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PP1 磷酸酶介导的延伸/终止因子交换协调转录终止。

Elongation/Termination Factor Exchange Mediated by PP1 Phosphatase Orchestrates Transcription Termination.

机构信息

Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.

Department of Chemistry, University of Oxford, Oxford OX1 3QU, UK.

出版信息

Cell Rep. 2018 Oct 2;25(1):259-269.e5. doi: 10.1016/j.celrep.2018.09.007.

Abstract

Termination of RNA polymerase II (Pol II) transcription is a key step that is important for 3' end formation of functional mRNA, mRNA release, and Pol II recycling. Even so, the underlying termination mechanism is not yet understood. Here, we demonstrate that the conserved and essential termination factor Seb1 is found on Pol II near the end of the RNA exit channel and the Rpb4/7 stalk. Furthermore, the Seb1 interaction surface with Pol II largely overlaps with that of the elongation factor Spt5. Notably, Seb1 co-transcriptional recruitment is dependent on Spt5 dephosphorylation by the conserved PP1 phosphatase Dis2, which also dephosphorylates threonine 4 within the Pol II heptad repeated C-terminal domain. We propose that Dis2 orchestrates the transition from elongation to termination phase during the transcription cycle by mediating elongation to termination factor exchange and dephosphorylation of Pol II C-terminal domain.

摘要

RNA 聚合酶 II(Pol II)转录的终止是一个关键步骤,对于功能性 mRNA 的 3' 端形成、mRNA 释放和 Pol II 循环至关重要。即便如此,潜在的终止机制尚不清楚。在这里,我们证明了保守且必需的终止因子 Seb1 存在于 Pol II 靠近 RNA 出口通道和 Rpb4/7 柄的末端。此外,Seb1 与 Pol II 的相互作用表面在很大程度上与延伸因子 Spt5 的相互作用表面重叠。值得注意的是,Seb1 的共转录募集依赖于保守的 PP1 磷酸酶 Dis2 对 Spt5 的去磷酸化,Dis2 还对 Pol II 七肽重复 C 端结构域内的苏氨酸 4 进行去磷酸化。我们提出 Dis2 通过介导延伸至终止因子的交换和 Pol II C 端结构域的去磷酸化来协调转录循环中从延伸到终止阶段的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8d9/6180485/de16afb3f3e6/fx1.jpg

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