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亚基因RNA聚合酶II相互作用组鉴定区域特异性转录延伸调节因子。

Subgenic Pol II interactomes identify region-specific transcription elongation regulators.

作者信息

Harlen Kevin M, Churchman L Stirling

机构信息

Department of Genetics, Harvard Medical School, Boston, MA, USA.

Department of Genetics, Harvard Medical School, Boston, MA, USA

出版信息

Mol Syst Biol. 2017 Jan 2;13(1):900. doi: 10.15252/msb.20167279.

DOI:10.15252/msb.20167279
PMID:28043953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5293154/
Abstract

Transcription, RNA processing, and chromatin-related factors all interact with RNA polymerase II (Pol II) to ensure proper timing and coordination of transcription and co-transcriptional processes. Many transcription elongation regulators must function simultaneously to coordinate these processes, yet few strategies exist to explore the complement of factors regulating specific stages of transcription. To this end, we developed a strategy to purify Pol II elongation complexes from subgenic regions of a single gene, namely the 5' and 3' regions, using sequences in the nascent RNA. Applying this strategy to Saccharomyces cerevisiae, we determined the specific set of factors that interact with Pol II at precise stages during transcription. We identify many known region-specific factors as well as determine unappreciated associations of regulatory factors during early and late stages of transcription. These data reveal a role for the transcription termination factor, Rai1, in regulating the early stages of transcription genome-wide and support the role of Bye1 as a negative regulator of early elongation. We also demonstrate a role for the ubiquitin ligase, Bre1, in regulating Pol II dynamics during the latter stages of transcription. These data and our approach to analyze subgenic transcription elongation complexes will shed new light on the myriad factors that regulate the different stages of transcription and coordinate co-transcriptional processes.

摘要

转录、RNA 加工和染色质相关因子均与 RNA 聚合酶 II(Pol II)相互作用,以确保转录及共转录过程的时间安排得当且协调有序。许多转录延伸调节因子必须同时发挥作用来协调这些过程,但用于探索调控转录特定阶段的因子互补情况的策略却很少。为此,我们开发了一种策略,利用新生 RNA 中的序列从单个基因的亚基因区域(即 5' 和 3' 区域)纯化 Pol II 延伸复合物。将该策略应用于酿酒酵母,我们确定了在转录精确阶段与 Pol II 相互作用的特定因子集。我们鉴定出许多已知的区域特异性因子,并确定了转录早期和晚期调控因子之间未被重视的关联。这些数据揭示了转录终止因子 Rai1 在全基因组范围内调控转录早期阶段的作用,并支持 Bye1 作为早期延伸负调控因子的作用。我们还证明了泛素连接酶 Bre1 在转录后期调控 Pol II 动态方面的作用。这些数据以及我们分析亚基因转录延伸复合物的方法将为调控转录不同阶段并协调共转录过程的众多因子提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/db4f33950ef0/MSB-13-900-g010.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/ac64d339d8c5/MSB-13-900-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/db4f33950ef0/MSB-13-900-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/beb9c9282ffe/MSB-13-900-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/e2a150be8707/MSB-13-900-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/132a6dd88acd/MSB-13-900-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/5ac88a3f2a99/MSB-13-900-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/c242d7083941/MSB-13-900-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/f06237dc4ea3/MSB-13-900-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76d/5293154/55d2ffbad91c/MSB-13-900-g009.jpg
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