paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5 | INTRODUCTION | 0 | null | null | 17,088,291 | null | We show that both long 3′-UTRs and introns located in the 3′-UTR act as NMD cis factors. | null | 88 | 7,900 | 0 | false | null | null | We show that both long 3′-UTRs and introns located in the 3′-UTR act as NMD cis factors. | true | true | true | true | true | 1,285 |
5 | INTRODUCTION | 0 | null | null | 17,088,291 | null | As both long 3′-UTR-based and intron-based PTC identification systems operate in plants as well as in animals, it is likely that these PTC definition systems already existed in the common ancestor of stem eukaryotes. | null | 216 | 7,901 | 0 | false | null | null | As both long 3′-UTR-based and intron-based PTC identification systems operate in plants as well as in animals, it is likely that these PTC definition systems already existed in the common ancestor of stem eukaryotes. | true | true | true | true | true | 1,285 |
5 | INTRODUCTION | 0 | null | null | 17,088,291 | null | We have also shown that tethering of UPF1 to either the 5′- or 3′-UTR causes a dramatic reduction of target mRNA levels, suggesting that in plants, UPF1 binds to the mRNA in a late, irreversible phase of NMD. | null | 208 | 7,902 | 0 | false | null | null | We have also shown that tethering of UPF1 to either the 5′- or 3′-UTR causes a dramatic reduction of target mRNA levels, suggesting that in plants, UPF1 binds to the mRNA in a late, irreversible phase of NMD. | true | true | true | true | true | 1,285 |
0 | DISCUSSION | 1 | 54 | [
"b54"
] | 17,088,291 | pmid-15448691|pmid-14690598|pmid-12609035 | Transient assays have been efficiently used to analyse NMD in mammalian and Drosophila cells. | [
"54"
] | 93 | 7,903 | 0 | false | Transient assays have been efficiently used to analyse NMD in mammalian and Drosophila cells. | [] | Transient assays have been efficiently used to analyse NMD in mammalian and Drosophila cells. | true | true | true | true | true | 1,286 |
0 | DISCUSSION | 1 | 54 | [
"b54"
] | 17,088,291 | pmid-15448691|pmid-14690598|pmid-12609035 | As transient NMD assays often require the expression of several different genes, and because agroinfiltration is the best method to co-express many different genes in plants (54), we have established an agroinfiltration-based transient plant NMD test system. | [
"54"
] | 258 | 7,904 | 1 | false | As transient NMD assays often require the expression of several different genes, and because agroinfiltration is the best method to co-express many different genes in plants, we have established an agroinfiltration-based transient plant NMD test system. | [
"54"
] | As transient NMD assays often require the expression of several different genes, and because agroinfiltration is the best method to co-express many different genes in plants, we have established an agroinfiltration-based transient plant NMD test system. | true | true | true | true | true | 1,286 |
0 | DISCUSSION | 1 | 54 | [
"b54"
] | 17,088,291 | pmid-15448691|pmid-14690598|pmid-12609035 | We have shown that PTC-containing mRNAs accumulate to low levels relative to wild-type controls and that the levels of PTC-containing mRNAs are selectively increased by cycloheximide treatment or by co-expressing UPF1DN, a dominant-negative mutant of plant UPF1 (Figures 2 and 3). | [
"54"
] | 280 | 7,905 | 0 | false | We have shown that PTC-containing mRNAs accumulate to low levels relative to wild-type controls and that the levels of PTC-containing mRNAs are selectively increased by cycloheximide treatment or by co-expressing UPF1DN, a dominant-negative mutant of plant UPF1 (Figures 2 and 3). | [] | We have shown that PTC-containing mRNAs accumulate to low levels relative to wild-type controls and that the levels of PTC-containing mRNAs are selectively increased by cycloheximide treatment or by co-expressing UPF1DN, a dominant-negative mutant of plant UPF1 (Figures 2 and 3). | true | true | true | true | true | 1,286 |
0 | DISCUSSION | 1 | 54 | [
"b54"
] | 17,088,291 | pmid-15448691|pmid-14690598|pmid-12609035 | These data indicate that in agroinfiltrated leaves PTC-containing mRNAs were targeted by NMD. | [
"54"
] | 93 | 7,906 | 0 | false | These data indicate that in agroinfiltrated leaves PTC-containing mRNAs were targeted by NMD. | [] | These data indicate that in agroinfiltrated leaves PTC-containing mRNAs were targeted by NMD. | true | true | true | true | true | 1,286 |
0 | DISCUSSION | 1 | 54 | [
"b54"
] | 17,088,291 | pmid-15448691|pmid-14690598|pmid-12609035 | We think that this versatile transient NMD test system, in combination with UPF1DN co-expression and λN-boxB tethering assay systems can become useful tools to characterize plant NMD. | [
"54"
] | 183 | 7,907 | 0 | false | We think that this versatile transient NMD test system, in combination with UPF1DN co-expression and λN-boxB tethering assay systems can become useful tools to characterize plant NMD. | [] | We think that this versatile transient NMD test system, in combination with UPF1DN co-expression and λN-boxB tethering assay systems can become useful tools to characterize plant NMD. | true | true | true | true | true | 1,286 |
1 | DISCUSSION | 0 | null | null | 17,088,291 | pmid-15040442|pmid-16043493|pmid-15525991|pmid-16246174 | Taking the advantage of the transient NMD test system, we have identified the cis elements of plant NMD. | null | 104 | 7,908 | 0 | false | null | null | Taking the advantage of the transient NMD test system, we have identified the cis elements of plant NMD. | true | true | true | true | true | 1,287 |
1 | DISCUSSION | 0 | null | null | 17,088,291 | pmid-15040442|pmid-16043493|pmid-15525991|pmid-16246174 | We found that in plants stop codons are identified as PTC if the 3′-UTR is unusually long or if an intron is located in the 3′-UTR. | null | 131 | 7,909 | 0 | false | null | null | We found that in plants stop codons are identified as PTC if the 3′-UTR is unusually long or if an intron is located in the 3′-UTR. | true | true | true | true | true | 1,287 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Previous reports have shown that intronless mRNAs can be degraded by NMD in plants (30–33). | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 91 | 7,910 | 0 | false | Previous reports have shown that intronless mRNAs can be degraded by NMD in plants. | [
"30–33"
] | Previous reports have shown that intronless mRNAs can be degraded by NMD in plants. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Consistently we have found that intronless mRNAs are targeted by NMD if a PTC is introduced into the coding region or if stuffer sequences are cloned into their 3′-UTRs (Figures 2 and 3). | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 187 | 7,911 | 0 | false | Consistently we have found that intronless mRNAs are targeted by NMD if a PTC is introduced into the coding region or if stuffer sequences are cloned into their 3′-UTRs (Figures 2 and 3). | [] | Consistently we have found that intronless mRNAs are targeted by NMD if a PTC is introduced into the coding region or if stuffer sequences are cloned into their 3′-UTRs. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | As we failed to identify DSE-like destabilizing sequences and because insertion of either bacterial or plant sequences into the 3′-UTR triggered NMD, we concluded that long 3′-UTR subjected intronless mRNAs to NMD in plants. | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 224 | 7,912 | 0 | false | As we failed to identify DSE-like destabilizing sequences and because insertion of either bacterial or plant sequences into the 3′-UTR triggered NMD, we concluded that long 3′-UTR subjected intronless mRNAs to NMD in plants. | [] | As we failed to identify DSE-like destabilizing sequences and because insertion of either bacterial or plant sequences into the 3′-UTR triggered NMD, we concluded that long 3′-UTR subjected intronless mRNAs to NMD in plants. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Moreover, we have shown that this effect was size-dependent, mRNAs with longer 3′-UTR were more effectively targeted by NMD than transcript with shorter 3′-UTR (Figure 3D and E). | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 178 | 7,913 | 0 | false | Moreover, we have shown that this effect was size-dependent, mRNAs with longer 3′-UTR were more effectively targeted by NMD than transcript with shorter 3′-UTR (Figure 3D and E). | [] | Moreover, we have shown that this effect was size-dependent, mRNAs with longer 3′-UTR were more effectively targeted by NMD than transcript with shorter 3′-UTR. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Long 3′-UTR could also trigger NMD in yeast, Drosophila, worm and mammalian cells (8,17–19,55). | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 95 | 7,914 | 0 | false | Long 3′-UTR could also trigger NMD in yeast, Drosophila, worm and mammalian cells. | [
"8,17–19,55"
] | Long 3′-UTR could also trigger NMD in yeast, Drosophila, worm and mammalian cells. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 9 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | The faux UTR model of yeast NMD suggests that long 3′-UTR (and perhaps other unusual 3′-UTRs) causes aberrant translation termination and that aberrant termination leads to the formation of a functional NMD complex (9). | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 219 | 7,915 | 1 | false | The faux UTR model of yeast NMD suggests that long 3′-UTR (and perhaps other unusual 3′-UTRs) causes aberrant translation termination and that aberrant termination leads to the formation of a functional NMD complex. | [
"9"
] | The faux UTR model of yeast NMD suggests that long 3′-UTR (and perhaps other unusual 3′-UTRs) causes aberrant translation termination and that aberrant termination leads to the formation of a functional NMD complex. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | As PTC-containing yeast mRNAs can be protected from NMD if PABP is tethered downstream of the stop codon, it is likely that long 3′-UTR causes aberrant termination by inhibiting the interaction of terminating ribosome with PABP ( | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 229 | 7,916 | 0 | false | As PTC-containing yeast mRNAs can be protected from NMD if PABP is tethered downstream of the stop codon, it is likely that long 3′-UTR causes aberrant termination by inhibiting the interaction of terminating ribosome with PABP ( | [] | As PTC-containing yeast mRNAs can be protected from NMD if PABP is tethered downstream of the stop codon, it is likely that long 3′-UTR causes aberrant termination by inhibiting the interaction of terminating ribosome with PABP ( | true | true | false | true | false | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Our findings that long 3′-UTR triggers NMD in plants and that this transcript destabilizing effect depends on the size of the 3′-UTR can be explained if the faux UTR model is valid for plant NMD. | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 195 | 7,917 | 0 | false | Our findings that long 3′-UTR triggers NMD in plants and that this transcript destabilizing effect depends on the size of the 3′-UTR can be explained if the faux UTR model is valid for plant NMD. | [] | Our findings that long 3′-UTR triggers NMD in plants and that this transcript destabilizing effect depends on the size of the 3′-UTR can be explained if the faux UTR model is valid for plant NMD. | true | true | true | true | true | 1,288 |
2 | DISCUSSION | 1 | 30 | [
"b30",
"b33",
"b8",
"b17",
"b19",
"b55",
"b9",
"b8"
] | 17,088,291 | pmid-12672499|pmid-15145352|pmid-11118221|pmid-15608055|pmid-9644970|pmid-7891717|pmid-10882134|pmid-15525991|pmid-12881430|pmid-8104846|pmid-16622410|pmid-15525991|pmid-16723977|pmid-2152115|pmid-10758507|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16246174|pmid-15525991 | Therefore, we suggest that aberrant translation termination also leads to NMD in plants and that increasing the distance between terminating ribosome and PABP results in aberrant termination. | [
"30",
"33",
"8",
"17",
"19",
"55",
"9",
"8"
] | 191 | 7,918 | 0 | false | Therefore, we suggest that aberrant translation termination also leads to NMD in plants and that increasing the distance between terminating ribosome and PABP results in aberrant termination. | [] | Therefore, we suggest that aberrant translation termination also leads to NMD in plants and that increasing the distance between terminating ribosome and PABP results in aberrant termination. | true | true | true | true | true | 1,288 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | Introns could also act as NMD cis elements in plants. | [
"56",
"57"
] | 53 | 7,919 | 0 | false | Introns could also act as NMD cis elements in plants. | [] | Introns could also act as NMD cis elements in plants. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | The finding that incorporation of Ls intron into the 3′-UTR of either the GFP or PHA-s transcripts subjects these mRNAs to NMD (Figure 4) supports this conclusion. | [
"56",
"57"
] | 163 | 7,920 | 0 | false | The finding that incorporation of Ls intron into the 3′-UTR of either the GFP or PHA-s transcripts subjects these mRNAs to NMD (Figure 4) supports this conclusion. | [] | The finding that incorporation of Ls intron into the 3′-UTR of either the GFP or PHA-s transcripts subjects these mRNAs to NMD (Figure 4) supports this conclusion. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | Moreover, the effect of plant introns on mRNA stability is position-dependent. | [
"56",
"57"
] | 78 | 7,921 | 0 | false | Moreover, the effect of plant introns on mRNA stability is position-dependent. | [] | Moreover, the effect of plant introns on mRNA stability is position-dependent. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | mRNAs carrying Ls intron 99 nt downstream of the stop codon were targeted by NMD, while transcripts carrying the same intron 28 nt downstream of the stop codon did not trigger NMD (Figure 4C and D). | [
"56",
"57"
] | 198 | 7,922 | 0 | false | mRNAs carrying Ls intron 99 nt downstream of the stop codon were targeted by NMD, while transcripts carrying the same intron 28 nt downstream of the stop codon did not trigger NMD (Figure 4C and D). | [] | mRNAs carrying Ls intron 99 nt downstream of the stop codon were targeted by NMD, while transcripts carrying the same intron 28 nt downstream of the stop codon did not trigger NMD (Figure 4C and D). | false | true | true | true | false | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | In mammals, introns located less than 50–55 nt downstream of the stop codon also fail to trigger NMD. | [
"56",
"57"
] | 101 | 7,923 | 0 | false | In mammals, introns located less than 50–55 nt downstream of the stop codon also fail to trigger NMD. | [] | In mammals, introns located less than 50–55 nt downstream of the stop codon also fail to trigger NMD. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | As 3′-UTR located introns trigger NMD in a similar position-dependent manner in both plants and mammals, we suggest that in plants, like in mammals, EJC connects splicing and NMD. | [
"56",
"57"
] | 179 | 7,924 | 0 | false | As 3′-UTR located introns trigger NMD in a similar position-dependent manner in both plants and mammals, we suggest that in plants, like in mammals, EJC connects splicing and NMD. | [] | As 3′-UTR located introns trigger NMD in a similar position-dependent manner in both plants and mammals, we suggest that in plants, like in mammals, EJC connects splicing and NMD. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | Indeed, the putative orthologs of most EJC components were identified in plants (56,57). | [
"56",
"57"
] | 88 | 7,925 | 0 | false | Indeed, the putative orthologs of most EJC components were identified in plants. | [
"56,57"
] | Indeed, the putative orthologs of most EJC components were identified in plants. | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | However, in plants, unlike in mammals, the 3′-UTR tethering of EJC proteins does not result in the decay of targeted mRNAs (Supplementary Figure 8). | [
"56",
"57"
] | 148 | 7,926 | 0 | false | However, in plants, unlike in mammals, the 3′-UTR tethering of EJC proteins does not result in the decay of targeted mRNAs (Supplementary Figure 8). | [] | However, in plants, unlike in mammals, the 3′-UTR tethering of EJC proteins does not result in the decay of targeted mRNAs (Supplementary Figure 8). | true | true | true | true | true | 1,289 |
3 | DISCUSSION | 1 | 56 | [
"b56",
"b57"
] | 17,088,291 | pmid-15901503|pmid-16141059|pmid-16289965|pmid-16280547|pmid-15496452 | Therefore further experiments are required to prove that plant EJCs are directly involved in NMD. | [
"56",
"57"
] | 97 | 7,927 | 0 | false | Therefore further experiments are required to prove that plant EJCs are directly involved in NMD. | [] | Therefore further experiments are required to prove that plant EJCs are directly involved in NMD. | true | true | true | true | true | 1,289 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | Our data that introns can act as NMD cis elements in plants are apparently conflicting with previous studies. | [
"35",
"35",
"36",
"58"
] | 109 | 7,928 | 0 | false | Our data that introns can act as NMD cis elements in plants are apparently conflicting with previous studies. | [] | Our data that introns can act as NMD cis elements in plants are apparently conflicting with previous studies. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | It has been suggested that introns do not trigger NMD in barley, because mRNAs containing introns downstream of the PTC and the control transcripts accumulated to comparable levels (35). | [
"35",
"35",
"36",
"58"
] | 186 | 7,929 | 1 | false | It has been suggested that introns do not trigger NMD in barley, because mRNAs containing introns downstream of the PTC and the control transcripts accumulated to comparable levels. | [
"35"
] | It has been suggested that introns do not trigger NMD in barley, because mRNAs containing introns downstream of the PTC and the control transcripts accumulated to comparable levels. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | However, the transcript which was used as a control in that study also carried a PTC, therefore the control transcript could be also targeted by NMD. | [
"35",
"35",
"36",
"58"
] | 149 | 7,930 | 0 | false | However, the transcript which was used as a control in that study also carried a PTC, therefore the control transcript could be also targeted by NMD. | [] | However, the transcript which was used as a control in that study also carried a PTC, therefore the control transcript could be also targeted by NMD. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | Indeed, both the intron containing and control mRNAs accumulated to 3-fold lower levels than the corresponding wild-type mRNA (35). | [
"35",
"35",
"36",
"58"
] | 131 | 7,931 | 1 | false | Indeed, both the intron containing and control mRNAs accumulated to 3-fold lower levels than the corresponding wild-type mRNA. | [
"35"
] | Indeed, both the intron containing and control mRNAs accumulated to 3-fold lower levels than the corresponding wild-type mRNA. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 36 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | Rose has shown that incorporation of the Arabidopsis ubiquitin intron 80 nt downstream of the stop codon of the GUS reporter gene did not result in reduced reporter mRNA levels (36). | [
"35",
"35",
"36",
"58"
] | 182 | 7,932 | 1 | false | Rose has shown that incorporation of the Arabidopsis ubiquitin intron 80 nt downstream of the stop codon of the GUS reporter gene did not result in reduced reporter mRNA levels. | [
"36"
] | Rose has shown that incorporation of the Arabidopsis ubiquitin intron 80 nt downstream of the stop codon of the GUS reporter gene did not result in reduced reporter mRNA levels. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 58 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | In mammals, different introns trigger NMD with different efficiency (58). | [
"35",
"35",
"36",
"58"
] | 73 | 7,933 | 1 | false | In mammals, different introns trigger NMD with different efficiency. | [
"58"
] | In mammals, different introns trigger NMD with different efficiency. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | It is possible that the Ls intron triggers NMD more effectively than the ubiquitin intron. | [
"35",
"35",
"36",
"58"
] | 90 | 7,934 | 0 | false | It is possible that the Ls intron triggers NMD more effectively than the ubiquitin intron. | [] | It is possible that the Ls intron triggers NMD more effectively than the ubiquitin intron. | true | true | true | true | true | 1,290 |
4 | DISCUSSION | 1 | 35 | [
"b35",
"b35",
"b36",
"b58"
] | 17,088,291 | pmid-15951220|pmid-8980474|pmid-12672499|pmid-16098107|pmid-16540482|pmid-16813578|pmid-16540482|pmid-16740149|pmid-2152115|pmid-10758507|pmid-11244118|pmid-15331098|pmid-15546357|pmid-15331098|pmid-15331098|pmid-15546357|pmid-16116435 | Alternatively, in plants, the intron should be more distant than 80 nt downstream of the stop codon to trigger NMD. | [
"35",
"35",
"36",
"58"
] | 115 | 7,935 | 0 | false | Alternatively, in plants, the intron should be more distant than 80 nt downstream of the stop codon to trigger NMD. | [] | Alternatively, in plants, the intron should be more distant than 80 nt downstream of the stop codon to trigger NMD. | true | true | true | true | true | 1,290 |
5 | DISCUSSION | 0 | null | null | 17,088,291 | null | Identification of NMD cis elements allows the recognition of Arabidopsis genes, which could be regulated by NMD. | null | 112 | 7,936 | 0 | false | null | null | Identification of NMD cis elements allows the recognition of Arabidopsis genes, which could be regulated by NMD. | true | true | true | true | true | 1,291 |
5 | DISCUSSION | 0 | null | null | 17,088,291 | null | Structural targets could be transcripts with an intron in the 3′-UTR, mRNAs with long 3′-UTR, or mRNAs containing an upstream ORF (uORF) in their 5′-UTR region. | null | 160 | 7,937 | 0 | false | null | null | Structural targets could be transcripts with an intron in the 3′-UTR, mRNAs with long 3′-UTR, or mRNAs containing an upstream ORF (uORF) in their 5′-UTR region. | true | true | true | true | true | 1,291 |
5 | DISCUSSION | 0 | null | null | 17,088,291 | null | In silico analysis shows, that ∼30% of plant mRNAs contain uORF. | null | 64 | 7,938 | 0 | false | null | null | In silico analysis shows, that ∼30% of plant mRNAs contain uORF. | true | true | true | true | true | 1,291 |
5 | DISCUSSION | 0 | null | null | 17,088,291 | null | We have identified ∼1000 genes whose 3′-UTRs are longer than 500 nt and found that 3.6% of all Arabidopsis genes contain intron in their 3′-UTRs (list of genes are available as Additional Materials, ). | null | 201 | 7,939 | 0 | false | null | null | We have identified ∼1000 genes whose 3′-UTRs are longer than 500 nt and found that 3.6% of all Arabidopsis genes contain intron in their 3′-UTRs (list of genes are available as Additional Materials, ). | true | true | true | true | true | 1,291 |
5 | DISCUSSION | 0 | null | null | 17,088,291 | null | Therefore, it is likely that NMD also plays a role in regulation of many wild-type genes in plants. | null | 99 | 7,940 | 0 | false | null | null | Therefore, it is likely that NMD also plays a role in regulation of many wild-type genes in plants. | true | true | true | true | true | 1,291 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
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"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | As the putative UPF1, 2 and 3 orthologs can be identified in each eukaryotic lineages and because the NMD system has not been found in prokaryotes, it is likely that NMD evolved in the stem eukaryotes (56,59). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 209 | 7,941 | 0 | false | As the putative UPF1, 2 and 3 orthologs can be identified in each eukaryotic lineages and because the NMD system has not been found in prokaryotes, it is likely that NMD evolved in the stem eukaryotes. | [
"56,59"
] | As the putative UPF1, 2 and 3 orthologs can be identified in each eukaryotic lineages and because the NMD system has not been found in prokaryotes, it is likely that NMD evolved in the stem eukaryotes. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | However, the evolution of NMD system is not well understood. | [
"56",
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"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 60 | 7,942 | 0 | false | However, the evolution of NMD system is not well understood. | [] | However, the evolution of NMD system is not well understood. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 19 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
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] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | As long 3′-UTR triggers NMD in yeast, Drosophila, worm and human cells (8,17–19,55), it has been suggested that this PTC definition system is ancient (19), perhaps it was already present in the stem eukaryotes. | [
"56",
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"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 210 | 7,943 | 1 | false | As long 3′-UTR triggers NMD in yeast, Drosophila, worm and human cells, it has been suggested that this PTC definition system is ancient, perhaps it was already present in the stem eukaryotes. | [
"8,17–19,55",
"19"
] | As long 3′-UTR triggers NMD in yeast, Drosophila, worm and human cells, it has been suggested that this PTC definition system is ancient, perhaps it was already present in the stem eukaryotes. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | Our result that long 3′-UTRs also trigger NMD in plants supports this hypothesis. | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 81 | 7,944 | 0 | false | Our result that long 3′-UTRs also trigger NMD in plants supports this hypothesis. | [] | Our result that long 3′-UTRs also trigger NMD in plants supports this hypothesis. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | The evolution of intron-based PTC definition is more debated. | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 61 | 7,945 | 0 | false | The evolution of intron-based PTC definition is more debated. | [] | The evolution of intron-based PTC definition is more debated. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 11 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | Based on the findings that introns are not NMD cis elements in yeast or Drosophila, it has been suggested that the intron-based PTC definition evolved late, only when alternative splicing had become dominant in certain animal lineages (11). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 240 | 7,946 | 1 | false | Based on the findings that introns are not NMD cis elements in yeast or Drosophila, it has been suggested that the intron-based PTC definition evolved late, only when alternative splicing had become dominant in certain animal lineages. | [
"11"
] | Based on the findings that introns are not NMD cis elements in yeast or Drosophila, it has been suggested that the intron-based PTC definition evolved late, only when alternative splicing had become dominant in certain animal lineages. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | An alternative model of NMD evolution has proposed that the intron-based PTC definition has already operated in the stem eukaryotes. | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 132 | 7,947 | 0 | false | An alternative model of NMD evolution has proposed that the intron-based PTC definition has already operated in the stem eukaryotes. | [] | An alternative model of NMD evolution has proposed that the intron-based PTC definition has already operated in the stem eukaryotes. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | This model suggests that splicing and NMD were coupled by the EJC in these ancient organisms (56,59). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 101 | 7,948 | 0 | false | This model suggests that splicing and NMD were coupled by the EJC in these ancient organisms. | [
"56,59"
] | This model suggests that splicing and NMD were coupled by the EJC in these ancient organisms. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | As the EJC components (56) and many introns (60,61) are highly conserved in eukaryotes, this model hypothesizes that in stem eukaryotes EJC-based NMD could efficiently eliminate PTC-containing mRNAs of spliced transcripts, thereby providing primary positive selection for the intron containing alleles. | [
"56",
"59",
"8",
"17",
"19",
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"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 302 | 7,949 | 1 | false | As the EJC components and many introns are highly conserved in eukaryotes, this model hypothesizes that in stem eukaryotes EJC-based NMD could efficiently eliminate PTC-containing mRNAs of spliced transcripts, thereby providing primary positive selection for the intron containing alleles. | [
"56",
"60,61"
] | As the EJC components and many introns are highly conserved in eukaryotes, this model hypothesizes that in stem eukaryotes EJC-based NMD could efficiently eliminate PTC-containing mRNAs of spliced transcripts, thereby providing primary positive selection for the intron containing alleles. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | Consequently, NMD facilitated the rapid spreading of ancient introns in stem eukaryotes (56,59). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 96 | 7,950 | 0 | false | Consequently, NMD facilitated the rapid spreading of ancient introns in stem eukaryotes. | [
"56,59"
] | Consequently, NMD facilitated the rapid spreading of ancient introns in stem eukaryotes. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | The finding that 3′-UTR located introns trigger NMD in a position-dependent manner in plants is consistent with this model. | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 123 | 7,951 | 0 | false | The finding that 3′-UTR located introns trigger NMD in a position-dependent manner in plants is consistent with this model. | [] | The finding that 3′-UTR located introns trigger NMD in a position-dependent manner in plants is consistent with this model. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
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"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | This model also predicts that introns should be ∼evenly distributed within the coding regions (56,59). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 102 | 7,952 | 0 | false | This model also predicts that introns should be ∼evenly distributed within the coding regions. | [
"56,59"
] | This model also predicts that introns should be ∼evenly distributed within the coding regions. | true | true | true | true | true | 1,292 |
6 | DISCUSSION | 1 | 56 | [
"b56",
"b59",
"b8",
"b17",
"b19",
"b55",
"b19",
"b11",
"b56",
"b59",
"b56",
"b60",
"b61",
"b56",
"b59",
"b56",
"b59",
"b59",
"b62"
] | 17,088,291 | pmid-16280547|pmid-12654936|pmid-15525991|pmid-12881430|pmid-16622410|pmid-11672865|pmid-16622410|pmid-15145352|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12956953|pmid-15687506|pmid-16280547|pmid-12654936|pmid-16280547|pmid-12654936|pmid-12654936|pmid-12468090 | Indeed, we and others (59,62) have shown that plant introns are distributed relatively equally along the coding regions except the very 5′ and 3′ regions (Additional Materials). | [
"56",
"59",
"8",
"17",
"19",
"55",
"19",
"11",
"56",
"59",
"56",
"60",
"61",
"56",
"59",
"56",
"59",
"59",
"62"
] | 177 | 7,953 | 0 | false | Indeed, we and others have shown that plant introns are distributed relatively equally along the coding regions except the very 5′ and 3′ regions (Additional Materials). | [
"59,62"
] | Indeed, we and others have shown that plant introns are distributed relatively equally along the coding regions except the very 5′ and 3′ regions (Additional Materials). | true | true | true | true | true | 1,292 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | Taken together, our findings suggest that both long 3′-UTR and intron-based PTC definition systems could operate in stem eukaryotes. | null | 132 | 7,954 | 0 | false | null | null | Taken together, our findings suggest that both long 3′-UTR and intron-based PTC definition systems could operate in stem eukaryotes. | true | true | true | true | true | 1,293 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | In lineages, in which intron loss dominated (yeast, Drosophila etc. | null | 67 | 7,955 | 0 | false | null | null | In lineages, in which intron loss dominated (yeast, Drosophila etc. | true | true | true | true | true | 1,293 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | ), splicing and NMD could be evolutionarily uncoupled, thus long 3′-UTR became the dominant NMD cis element. | null | 108 | 7,956 | 0 | false | null | null | ), splicing and NMD could be evolutionarily uncoupled, thus long 3′-UTR became the dominant NMD cis element. | false | false | true | true | false | 1,293 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | In contrast, in the extremely intron-dense lineages, where alternative splicing is very widely used (mammals), introns could become the more efficient and dominating NMD cis elements. | null | 183 | 7,957 | 0 | false | null | null | In contrast, in the extremely intron-dense lineages, where alternative splicing is very widely used (mammals), introns could become the more efficient and dominating NMD cis elements. | true | true | true | true | true | 1,293 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | Although, plants are intron-dense organisms, intronless genes are also frequently found in the plant genome, thus NMD machinery has evolved under dual constrains, it should efficiently identify PTC-containing mRNAs derived from either intronless or intron containing genes. | null | 273 | 7,958 | 0 | false | null | null | Although, plants are intron-dense organisms, intronless genes are also frequently found in the plant genome, thus NMD machinery has evolved under dual constrains, it should efficiently identify PTC-containing mRNAs derived from either intronless or intron containing genes. | true | true | true | true | true | 1,293 |
7 | DISCUSSION | 0 | null | null | 17,088,291 | null | Therefore, both long 3′-UTR and intron-based PTC recognition machinery should work efficiently in plants. | null | 105 | 7,959 | 0 | false | null | null | Therefore, both long 3′-UTR and intron-based PTC recognition machinery should work efficiently in plants. | true | true | true | true | true | 1,293 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b9",
"b4",
"b7",
"b10",
"b8",
"b11"
] | 17,175,534 | pmid-9421513|pmid-12060689|pmid-10556321|pmid-12783628|pmid-16314312|pmid-9461475|pmid-15070404 | Since the mid-1990s, automated gene finders for prokaryotic genome sequences have become available that allow the unsupervised discovery of genes from raw genomic sequence (1–9). | [
"1",
"9",
"4",
"7",
"10",
"8",
"11"
] | 178 | 7,960 | 0 | false | Since the mid-1990s, automated gene finders for prokaryotic genome sequences have become available that allow the unsupervised discovery of genes from raw genomic sequence. | [
"1–9"
] | Since the mid-1990s, automated gene finders for prokaryotic genome sequences have become available that allow the unsupervised discovery of genes from raw genomic sequence. | true | true | true | true | true | 1,294 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b9",
"b4",
"b7",
"b10",
"b8",
"b11"
] | 17,175,534 | pmid-9421513|pmid-12060689|pmid-10556321|pmid-12783628|pmid-16314312|pmid-9461475|pmid-15070404 | This accomplishment, accompanied by impressive values of accuracy, has made prokaryotic gene prediction one of the showcases of computational biology. | [
"1",
"9",
"4",
"7",
"10",
"8",
"11"
] | 150 | 7,961 | 0 | false | This accomplishment, accompanied by impressive values of accuracy, has made prokaryotic gene prediction one of the showcases of computational biology. | [] | This accomplishment, accompanied by impressive values of accuracy, has made prokaryotic gene prediction one of the showcases of computational biology. | true | true | true | true | true | 1,294 |
0 | INTRODUCTION | 1 | 4 | [
"b1",
"b9",
"b4",
"b7",
"b10",
"b8",
"b11"
] | 17,175,534 | pmid-9421513|pmid-12060689|pmid-10556321|pmid-12783628|pmid-16314312|pmid-9461475|pmid-15070404 | Subsequent developments have focused mostly on the introduction of novel techniques to more accurately capture sequence composition (4), modeling of the gene structure (7,10) and development of models that allow the unsupervised discovery of multiple gene classes (8,11). | [
"1",
"9",
"4",
"7",
"10",
"8",
"11"
] | 271 | 7,962 | 1 | false | Subsequent developments have focused mostly on the introduction of novel techniques to more accurately capture sequence composition, modeling of the gene structure and development of models that allow the unsupervised discovery of multiple gene classes. | [
"4",
"7,10",
"8,11"
] | Subsequent developments have focused mostly on the introduction of novel techniques to more accurately capture sequence composition, modeling of the gene structure and development of models that allow the unsupervised discovery of multiple gene classes. | true | true | true | true | true | 1,294 |
1 | INTRODUCTION | 1 | 6 | [
"b6",
"b12",
"b13"
] | 17,175,534 | pmid-12626720|pmid-14988122|pmid-14965344 | Because of the high accuracy initially reported for most programs, some might consider prokaryotic gene prediction solved, but from the point of a practitioner, this is not quite the case yet. | [
"6",
"12",
"13"
] | 192 | 7,963 | 0 | false | Because of the high accuracy initially reported for most programs, some might consider prokaryotic gene prediction solved, but from the point of a practitioner, this is not quite the case yet. | [] | Because of the high accuracy initially reported for most programs, some might consider prokaryotic gene prediction solved, but from the point of a practitioner, this is not quite the case yet. | true | true | true | true | true | 1,295 |
1 | INTRODUCTION | 1 | 6 | [
"b6",
"b12",
"b13"
] | 17,175,534 | pmid-12626720|pmid-14988122|pmid-14965344 | For some programs the predictive accuracy is uncertain, as they have not been re-evaluated since the original evaluation on a handful of genomes. | [
"6",
"12",
"13"
] | 145 | 7,964 | 0 | false | For some programs the predictive accuracy is uncertain, as they have not been re-evaluated since the original evaluation on a handful of genomes. | [] | For some programs the predictive accuracy is uncertain, as they have not been re-evaluated since the original evaluation on a handful of genomes. | true | true | true | true | true | 1,295 |
1 | INTRODUCTION | 1 | 6 | [
"b6",
"b12",
"b13"
] | 17,175,534 | pmid-12626720|pmid-14988122|pmid-14965344 | The recent development of techniques that improve predictions by combining the output of multiple programs (6,12,13) shows that accuracy can be increased. | [
"6",
"12",
"13"
] | 154 | 7,965 | 0 | false | The recent development of techniques that improve predictions by combining the output of multiple programs shows that accuracy can be increased. | [
"6,12,13"
] | The recent development of techniques that improve predictions by combining the output of multiple programs shows that accuracy can be increased. | true | true | true | true | true | 1,295 |
1 | INTRODUCTION | 1 | 6 | [
"b6",
"b12",
"b13"
] | 17,175,534 | pmid-12626720|pmid-14988122|pmid-14965344 | Another issue is that some programs are only accessible via a web interface, which for genome projects—due to the confidentiality of the data—is frequently not an option. | [
"6",
"12",
"13"
] | 170 | 7,966 | 0 | false | Another issue is that some programs are only accessible via a web interface, which for genome projects—due to the confidentiality of the data—is frequently not an option. | [] | Another issue is that some programs are only accessible via a web interface, which for genome projects—due to the confidentiality of the data—is frequently not an option. | true | true | true | true | true | 1,295 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | Here we describe our novel gene finder GISMO (Gene Identification using a Support Vector Machine for ORF classification), which is freely available under the GPL license. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 170 | 7,967 | 0 | false | Here we describe our novel gene finder GISMO (Gene Identification using a Support Vector Machine for ORF classification), which is freely available under the GPL license. | [] | Here we describe our novel gene finder GISMO (Gene Identification using a Support Vector Machine for ORF classification), which is freely available under the GPL license. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | GISMO has high classification accuracy: it is very sensitive, meaning that it identifies most known genes, and specific, i.e. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 125 | 7,968 | 0 | false | GISMO has high classification accuracy: it is very sensitive, meaning that it identifies most known genes, and specific, i.e. | [] | GISMO has high classification accuracy: it is very sensitive, meaning that it identifies most known genes, and specific, i.e. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | it produces reliable predictions. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 33 | 7,969 | 0 | false | it produces reliable predictions. | [] | it produces reliable predictions. | false | true | true | true | false | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | Our program combines a hidden Markov model (HMM)-based search for protein domains with a support vector machine (SVM) to identify coding regions based on sequence composition. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 175 | 7,970 | 0 | false | Our program combines a hidden Markov model (HMM)-based search for protein domains with a support vector machine (SVM) to identify coding regions based on sequence composition. | [] | Our program combines a hidden Markov model (HMM)-based search for protein domains with a support vector machine (SVM) to identify coding regions based on sequence composition. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | An advantage of the HMM-based search for protein domains compared with pair-wise sequence searches is the higher accuracy in discriminating between signal and noise for protein family members (14). | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 197 | 7,971 | 1 | false | An advantage of the HMM-based search for protein domains compared with pair-wise sequence searches is the higher accuracy in discriminating between signal and noise for protein family members. | [
"14"
] | An advantage of the HMM-based search for protein domains compared with pair-wise sequence searches is the higher accuracy in discriminating between signal and noise for protein family members. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | Also, genes with new orderings of known protein domains can be detected easily. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 79 | 7,972 | 0 | false | Also, genes with new orderings of known protein domains can be detected easily. | [] | Also, genes with new orderings of known protein domains can be detected easily. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | An SVM classifier is constructed for composition-based identification of protein-encoding genes. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 96 | 7,973 | 0 | false | An SVM classifier is constructed for composition-based identification of protein-encoding genes. | [] | An SVM classifier is constructed for composition-based identification of protein-encoding genes. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 20 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | The SVM is a machine learning technique with a strong theoretical foundation (15,16) that has been used to improve classification accuracy in biological applications such as the detection of protein family members (17–19), RNA and DNA binding proteins (20), and the functional classification of gene expression data (21)... | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 321 | 7,974 | 1 | false | The SVM is a machine learning technique with a strong theoretical foundation that has been used to improve classification accuracy in biological applications such as the detection of protein family members, RNA and DNA binding proteins, and the functional classification of gene expression data. | [
"15,16",
"17–19",
"20",
"21"
] | The SVM is a machine learning technique with a strong theoretical foundation that has been used to improve classification accuracy in biological applications such as the detection of protein family members, RNA and DNA binding proteins, and the functional classification of gene expression data. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | The SVM is a maximum margin classifier that can solve non-linear classification problems by learning an optimally separating hyperplane in a higher-dimensional feature space. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 174 | 7,975 | 0 | false | The SVM is a maximum margin classifier that can solve non-linear classification problems by learning an optimally separating hyperplane in a higher-dimensional feature space. | [] | The SVM is a maximum margin classifier that can solve non-linear classification problems by learning an optimally separating hyperplane in a higher-dimensional feature space. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | By use of non-linear kernel functions such as a Gaussian kernel, complex and non-linear decision functions can be learned by the SVM. | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 133 | 7,976 | 0 | false | By use of non-linear kernel functions such as a Gaussian kernel, complex and non-linear decision functions can be learned by the SVM. | [] | By use of non-linear kernel functions such as a Gaussian kernel, complex and non-linear decision functions can be learned by the SVM. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | Even if items of one class are clustered in multiple separate sub-regions in the input space they can be clearly separated from the other class (Figure 1). | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 155 | 7,977 | 0 | false | Even if items of one class are clustered in multiple separate sub-regions in the input space they can be clearly separated from the other class (Figure 1). | [] | Even if items of one class are clustered in multiple separate sub-regions in the input space they can be clearly separated from the other class. | true | true | true | true | true | 1,296 |
2 | INTRODUCTION | 1 | 14 | [
"b14",
"b15",
"b16",
"b17",
"b19",
"b20",
"b21",
"b22",
"b24"
] | 17,175,534 | pmid-9837738|NA|NA|pmid-14630658|pmid-11928508|pmid-12758155|pmid-10618406|pmid-10075995|pmid-10508724 | The learnt hyperplane allows accurate discrimination between classes that cannot be separated linearly in the input space, as may be the case when phenomena such as horizontal gene transfer, translational selection and leading/lagging strand biases influence the sequence composition of genes (22–24). | [
"14",
"15",
"16",
"17",
"19",
"20",
"21",
"22",
"24"
] | 301 | 7,978 | 0 | false | The learnt hyperplane allows accurate discrimination between classes that cannot be separated linearly in the input space, as may be the case when phenomena such as horizontal gene transfer, translational selection and leading/lagging strand biases influence the sequence composition of genes. | [
"22–24"
] | The learnt hyperplane allows accurate discrimination between classes that cannot be separated linearly in the input space, as may be the case when phenomena such as horizontal gene transfer, translational selection and leading/lagging strand biases influence the sequence composition of genes. | true | true | true | true | true | 1,296 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | Class boundaries learned by the SVM with different kernel functions. | [
"30"
] | 68 | 7,979 | 0 | false | Class boundaries learned by the SVM with different kernel functions. | [] | Class boundaries learned by the SVM with different kernel functions. | true | true | true | true | true | 1,297 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | Circles and crosses represent instances of a toy example training set. | [
"30"
] | 70 | 7,980 | 0 | false | Circles and crosses represent instances of a toy example training set. | [] | Circles and crosses represent instances of a toy example training set. | true | true | true | true | true | 1,297 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | Colored regions indicate the two classes learned by three example SVM applications. | [
"30"
] | 83 | 7,981 | 0 | false | Colored regions indicate the two classes learned by three example SVM applications. | [] | Colored regions indicate the two classes learned by three example SVM applications. | true | true | true | true | true | 1,297 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | (A) A linear decision function learned with a linear kernel. | [
"30"
] | 60 | 7,982 | 0 | false | (A) A linear decision function learned with a linear kernel. | [] | (A) A linear decision function learned with a linear kernel. | false | false | true | true | false | 1,297 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | (B) A polynomial kernel allows realization of a polynomial separating surface. | [
"30"
] | 78 | 7,983 | 0 | false | (B) A polynomial kernel allows realization of a polynomial separating surface. | [] | (B) A polynomial kernel allows realization of a polynomial separating surface. | false | false | true | true | false | 1,297 |
3 | INTRODUCTION | 1 | 30 | [
"b30"
] | 17,175,534 | NA | (C) With a Gaussian kernel the SVM can learn disjoint decision functions that surround a multitude of ‘islands’ of items from the same class (30). | [
"30"
] | 146 | 7,984 | 1 | false | (C) With a Gaussian kernel the SVM can learn disjoint decision functions that surround a multitude of ‘islands’ of items from the same class. | [
"30"
] | (C) With a Gaussian kernel the SVM can learn disjoint decision functions that surround a multitude of ‘islands’ of items from the same class. | false | false | true | true | false | 1,297 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | GISMO was evaluated with 165 prokaryotic chromosomes and 223 plasmid sequences. | [
"7",
"25"
] | 79 | 7,985 | 0 | false | GISMO was evaluated with 165 prokaryotic chromosomes and 223 plasmid sequences. | [] | GISMO was evaluated with 165 prokaryotic chromosomes and 223 plasmid sequences. | true | true | true | true | true | 1,298 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | For the chromosomal sequences, GISMO identified 94.3% of the genes (98.9% for genes with annotated function), and 94.3% of its predictions corresponded to annotated genes. | [
"7",
"25"
] | 171 | 7,986 | 0 | false | For the chromosomal sequences, GISMO identified 94.3% of the genes (98.9% for genes with annotated function), and 94.3% of its predictions corresponded to annotated genes. | [] | For the chromosomal sequences, GISMO identified 94.3% of the genes (98.9% for genes with annotated function), and 94.3% of its predictions corresponded to annotated genes. | true | true | true | true | true | 1,298 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | Several thousand of the new predictions for the published genomes are supported by extrinsic evidence, suggesting that these very probably are biologically active genes that are missing in the annotations. | [
"7",
"25"
] | 205 | 7,987 | 0 | false | Several thousand of the new predictions for the published genomes are supported by extrinsic evidence, suggesting that these very probably are biologically active genes that are missing in the annotations. | [] | Several thousand of the new predictions for the published genomes are supported by extrinsic evidence, suggesting that these very probably are biologically active genes that are missing in the annotations. | true | true | true | true | true | 1,298 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | We also address some of the most challenging problems for prokaryotic gene finders, including the correct identification of short genes (7,25) and of genes with atypical sequence composition and the prediction of genes when only little sequence material is available, as in the case of extrachromosomal replicons. | [
"7",
"25"
] | 313 | 7,988 | 0 | false | We also address some of the most challenging problems for prokaryotic gene finders, including the correct identification of short genes and of genes with atypical sequence composition and the prediction of genes when only little sequence material is available, as in the case of extrachromosomal replicons. | [
"7,25"
] | We also address some of the most challenging problems for prokaryotic gene finders, including the correct identification of short genes and of genes with atypical sequence composition and the prediction of genes when only little sequence material is available, as in the case of extrachromosomal replicons. | true | true | true | true | true | 1,298 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | The composition-based SVM, which uses vectors of sequence composition in the (low-dimensional) space of codon usage, is well suited for these tasks and achieved the highest classification accuracy for all cases when compared with two other popular, freely available programs. | [
"7",
"25"
] | 275 | 7,989 | 0 | false | The composition-based SVM, which uses vectors of sequence composition in the (low-dimensional) space of codon usage, is well suited for these tasks and achieved the highest classification accuracy for all cases when compared with two other popular, freely available programs. | [] | The composition-based SVM, which uses vectors of sequence composition in the (low-dimensional) space of codon usage, is well suited for these tasks and achieved the highest classification accuracy for all cases when compared with two other popular, freely available programs. | true | true | true | true | true | 1,298 |
4 | INTRODUCTION | 1 | 7 | [
"b7",
"b25"
] | 17,175,534 | pmid-12783628|pmid-16922601 | GISMO predictions for the 165 genomic sequences are available for download in GFF at . | [
"7",
"25"
] | 86 | 7,990 | 0 | false | GISMO predictions for the 165 genomic sequences are available for download in GFF at. | [] | GISMO predictions for the 165 genomic sequences are available for download in GFF at. | true | true | true | true | true | 1,298 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | P-TEFb plays a key role in RNA polymerase II elongation control (1–3). | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 70 | 7,991 | 1 | false | P-TEFb plays a key role in RNA polymerase II elongation control. | [
"1–3"
] | P-TEFb plays a key role in RNA polymerase II elongation control. | true | true | true | true | true | 1,299 |
0 | INTRODUCTION | 1 | 6 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | It is comprised of one of two isoforms of Cdk9 (4,5) and one of three cyclins, T1, T2 (6) or K (7) in humans. | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 109 | 7,992 | 1 | false | It is comprised of one of two isoforms of Cdk9 and one of three cyclins, T1, T2 or K in humans. | [
"4,5",
"6",
"7"
] | It is comprised of one of two isoforms of Cdk9 and one of three cyclins, T1, T2 or K in humans. | true | true | true | true | true | 1,299 |
0 | INTRODUCTION | 1 | 8 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | One of the major targets of the kinase activity of P-TEFb is the carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II (8), and this phosphorylation of the CTD by P-TEFb occurs during transcription elongation (9). | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 234 | 7,993 | 1 | false | One of the major targets of the kinase activity of P-TEFb is the carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II, and this phosphorylation of the CTD by P-TEFb occurs during transcription elongation. | [
"8",
"9"
] | One of the major targets of the kinase activity of P-TEFb is the carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II, and this phosphorylation of the CTD by P-TEFb occurs during transcription elongation. | true | true | true | true | true | 1,299 |
0 | INTRODUCTION | 1 | 10 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | P-TEFb also phosphorylates the negative transcription elongation factor DSIF (10), turning it into a positive elongation factor (11). | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 133 | 7,994 | 1 | false | P-TEFb also phosphorylates the negative transcription elongation factor DSIF, turning it into a positive elongation factor. | [
"10",
"11"
] | P-TEFb also phosphorylates the negative transcription elongation factor DSIF, turning it into a positive elongation factor. | true | true | true | true | true | 1,299 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | P-TEFb controls gene expression by regulating the fraction of RNA polymerase II molecules that generate full-length mRNAs. | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 122 | 7,995 | 0 | false | P-TEFb controls gene expression by regulating the fraction of RNA polymerase II molecules that generate full-length mRNAs. | [] | P-TEFb controls gene expression by regulating the fraction of RNA polymerase II molecules that generate full-length mRNAs. | true | true | true | true | true | 1,299 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B4",
"B12 B13 B14 B15 B16"
] | 17,395,637 | pmid-16959964|pmid-16885020|pmid-16720337|pmid-9334325|pmid-12706900|pmid-9593731|pmid-10574912|pmid-8900211|pmid-7759473|pmid-9450929|pmid-16427012|pmid-9334325|pmid-9334326|pmid-9649438|pmid-10384302|pmid-9491887|pmid-11545735 | In addition to its normal cellular role, P-TEFb has been shown to be recruited by viral transactivator Tat to the nascent viral transcript, TAR, near the promoter to enhance viral transcription, which is required for efficient HIV-1 replication (4,12–16). | [
"1–3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"4",
"12–16"
] | 255 | 7,996 | 0 | false | In addition to its normal cellular role, P-TEFb has been shown to be recruited by viral transactivator Tat to the nascent viral transcript, TAR, near the promoter to enhance viral transcription, which is required for efficient HIV-1 replication. | [
"4,12–16"
] | In addition to its normal cellular role, P-TEFb has been shown to be recruited by viral transactivator Tat to the nascent viral transcript, TAR, near the promoter to enhance viral transcription, which is required for efficient HIV-1 replication. | true | true | true | true | true | 1,299 |
1 | INTRODUCTION | 1 | 19–22 | [
"B17",
"B18",
"B19 B20 B21 B22",
"B16",
"B23",
"B24",
"B25",
"B26",
"B27",
"B17",
"B19",
"B22",
"B19",
"B28 B29 B30 B31"
] | 17,395,637 | pmid-11713533|pmid-11713532|pmid-12832472|pmid-14580347|pmid-15713661|pmid-15713662|pmid-11545735|pmid-12177005|pmid-12944920|pmid-12037670|pmid-16109377|pmid-16109376|pmid-11713533|pmid-12832472|pmid-15713662|pmid-12832472|pmid-15514168|pmid-12695656|pmid-12368904|pmid-14749500|pmid-16382153|pmid-1646389|pmid-1646389 | P-TEFb is uniquely regulated by the reversible association of a small nuclear RNA, 7SK (17,18) and one of two HEXIM proteins (19–22). | [
"17",
"18",
"19–22",
"16",
"23",
"24",
"25",
"26",
"27",
"17",
"19",
"22",
"19",
"28–31"
] | 133 | 7,997 | 1 | false | P-TEFb is uniquely regulated by the reversible association of a small nuclear RNA, 7SK and one of two HEXIM proteins. | [
"17,18",
"19–22"
] | P-TEFb is uniquely regulated by the reversible association of a small nuclear RNA, 7SK and one of two HEXIM proteins. | true | true | true | true | true | 1,300 |
1 | INTRODUCTION | 1 | 17 | [
"B17",
"B18",
"B19 B20 B21 B22",
"B16",
"B23",
"B24",
"B25",
"B26",
"B27",
"B17",
"B19",
"B22",
"B19",
"B28 B29 B30 B31"
] | 17,395,637 | pmid-11713533|pmid-11713532|pmid-12832472|pmid-14580347|pmid-15713661|pmid-15713662|pmid-11545735|pmid-12177005|pmid-12944920|pmid-12037670|pmid-16109377|pmid-16109376|pmid-11713533|pmid-12832472|pmid-15713662|pmid-12832472|pmid-15514168|pmid-12695656|pmid-12368904|pmid-14749500|pmid-16382153|pmid-1646389|pmid-1646389 | Glycerol gradient analyses of cell lysates indicate that two forms of P-TEFb exist in the cell. | [
"17",
"18",
"19–22",
"16",
"23",
"24",
"25",
"26",
"27",
"17",
"19",
"22",
"19",
"28–31"
] | 95 | 7,998 | 0 | false | Glycerol gradient analyses of cell lysates indicate that two forms of P-TEFb exist in the cell. | [] | Glycerol gradient analyses of cell lysates indicate that two forms of P-TEFb exist in the cell. | true | true | true | true | true | 1,300 |
1 | INTRODUCTION | 1 | 16 | [
"B17",
"B18",
"B19 B20 B21 B22",
"B16",
"B23",
"B24",
"B25",
"B26",
"B27",
"B17",
"B19",
"B22",
"B19",
"B28 B29 B30 B31"
] | 17,395,637 | pmid-11713533|pmid-11713532|pmid-12832472|pmid-14580347|pmid-15713661|pmid-15713662|pmid-11545735|pmid-12177005|pmid-12944920|pmid-12037670|pmid-16109377|pmid-16109376|pmid-11713533|pmid-12832472|pmid-15713662|pmid-12832472|pmid-15514168|pmid-12695656|pmid-12368904|pmid-14749500|pmid-16382153|pmid-1646389|pmid-1646389 | An active form of P-TEFb, free of HEXIM and 7SK, interacts with a variety of cellular factors, including NF-κB (16), c-Myc (23,24), MyoD (25) and Brd4 (26,27), to regulate gene transcription. | [
"17",
"18",
"19–22",
"16",
"23",
"24",
"25",
"26",
"27",
"17",
"19",
"22",
"19",
"28–31"
] | 191 | 7,999 | 1 | false | An active form of P-TEFb, free of HEXIM and 7SK, interacts with a variety of cellular factors, including NF-κB, c-Myc, MyoD and Brd4, to regulate gene transcription. | [
"16",
"23,24",
"25",
"26,27"
] | An active form of P-TEFb, free of HEXIM and 7SK, interacts with a variety of cellular factors, including NF-κB, c-Myc, MyoD and Brd4, to regulate gene transcription. | true | true | true | true | true | 1,300 |
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