A role for the CPF 3′-end processing machinery in RNAP II-dependent gene looping

被引:195
作者
Ansari, A [1 ]
Hampsey, M [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Biochem, Div Nucle Acids Res, Piscataway, NJ 08854 USA
关键词
CPF complex; gene loops; RNA polymerase II; Ssu72; transcription termination;
D O I
10.1101/gad.1362305
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The prevailing view of the RNA polymerase 11 (RNAP 11) transcription cycle is that RNAP 11 is recruited to the promoter, transcribes a linear DNA template, then terminates transcription and dissociates from the template. Subsequent rounds of transcription are thought to require de novo recruitment of RNAP 11 to the promoter. Several recent findings, including physical interaction of T-end processing factors with both promoter and terminator regions, challenge this concept. Here we report a physical association of promoter and terminator regions of the yeast BUD3 and SEN1 genes. These interactions are transcription-dependent, require the Ssu72 and Pta1 components of the CPF 3'-end processing complex, and require the phosphatase activity of Ssu72. We propose a model for RNAP 11 transcription in which promoter and terminator regions are juxtaposed, and that the resulting gene loops facilitate transcription reinitiation by the same molecule of RNAP 11 in a manner dependent upon Ssu72-mediated CTD dephosphorylation.
引用
收藏
页码:2969 / 2978
页数:10
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