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The role of Rad1 in coupling mRNA 3′-end processing to transcription termination:: implications for a unified allosteric-torpedo model
被引:141
作者:
Luo, WF
Johnson, AW
Bentley, DL
[1
]
机构:
[1] Univ Colorado, Sch Med, Hlth Sci Ctr, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Univ Texas, Dept Mol Genet & Microbiol, Austin, TX 78712 USA
关键词:
RNA pol II;
transcription termination;
Rat1;
3 '-end processing;
Pcf;
11;
D O I:
10.1101/gad.1409106
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The torpedo model of transcription termination by RNA polymerase II proposes that a 5'-3' RNA exonuclease enters at the poly(A) cleavage site, degrades the nascent RNA, and eventually displaces polymerase from the DNA. Cotranscriptional degradation of nascent RNA has not been directly demonstrated, however. Here we report that two exonucleases, Rat1 and Xrn1, both contribute to cotranscriptional degradation of nascent RNA, but this degradation is not sufficient to cause polymerase release. Unexpectedly, Rat1 functions in both 3'-end processing and termination by enhancing recruitment of T-end processing factors, including Pcf11 and Rna15. In addition, the cleavage factor Pcf11 reciprocally aids in recruitment of Rat1 to the elongation complex. Our results suggest a unified allosteric/torpedo model in which Rat1 is not a dedicated termination factor, but is an integrated component of the cleavage/polyadenylation apparatus.
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页码:954 / 965
页数:12
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