Ansari Athar, Hampsey Michael
Division of Nucleic Acids Research, Department of Biochemistry, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, 08854, USA.
Genes Dev. 2005 Dec 15;19(24):2969-78. doi: 10.1101/gad.1362305. Epub 2005 Nov 30.
The prevailing view of the RNA polymerase II (RNAP II) transcription cycle is that RNAP II 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 II to the promoter. Several recent findings, including physical interaction of 3'-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 II transcription in which promoter and terminator regions are juxtaposed, and that the resulting gene loops facilitate transcription reinitiation by the same molecule of RNAP II in a manner dependent upon Ssu72-mediated CTD dephosphorylation.
关于RNA聚合酶II(RNAP II)转录周期的主流观点是,RNAP II被招募到启动子,转录线性DNA模板,然后终止转录并从模板上解离。后续的转录轮次被认为需要将RNAP II重新招募到启动子。最近的一些发现,包括3'端加工因子与启动子和终止子区域的物理相互作用,对这一概念提出了挑战。在这里,我们报告了酵母BUD3和SEN1基因的启动子和终止子区域之间的物理关联。这些相互作用是转录依赖性的,需要CPF 3'端加工复合体的Ssu72和Pta1组分,并且需要Ssu72的磷酸酶活性。我们提出了一个RNAP II转录模型,其中启动子和终止子区域并列,并且由此产生的基因环以依赖于Ssu72介导的CTD去磷酸化的方式促进同一分子的RNAP II进行转录重新起始。