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多功能 Ccr4-Not 复合物直接促进转录延伸。

The multifunctional Ccr4-Not complex directly promotes transcription elongation.

机构信息

Department of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

Genes Dev. 2011 Mar 15;25(6):581-93. doi: 10.1101/gad.2020911.

Abstract

The Ccr4-Not complex has been implicated in the control of multiple steps of mRNA metabolism; however, its functions in transcription remain ambiguous. The discovery that Ccr4/Pop2 is the major cytoplasmic mRNA deadenylase and the detection of Not proteins within mRNA processing bodies have raised questions about the roles of the Ccr4-Not complex in transcription. Here we firmly establish Ccr4-Not as a positive elongation factor for RNA polymerase II (RNAPII). The Ccr4-Not complex is targeted to the coding region of genes in a transcription-dependent manner similar to RNAPII and promotes elongation in vivo. Furthermore, Ccr4-Not interacts directly with elongating RNAPII complexes and stimulates transcription elongation of arrested polymerase in vitro. Ccr4-Not can reactivate backtracked RNAPII using a mechanism different from that of the well-characterized elongation factor TFIIS. While not essential for its interaction with elongation complexes, Ccr4-Not interacts with the emerging transcript and promotes elongation in a manner dependent on transcript length, although this interaction is not required for it to bind RNAPII. Our comprehensive analysis shows that Ccr4-Not directly regulates transcription, and suggests it does so by promoting the resumption of elongation of arrested RNAPII when it encounters transcriptional blocks in vivo.

摘要

Ccr4-Not 复合物被牵涉到多个 mRNA 代谢步骤的调控中;然而,其在转录过程中的功能仍不明确。Ccr4/Pop2 是主要的细胞质 mRNA 脱腺苷酸化酶这一发现,以及在 mRNA 处理体中检测到 Not 蛋白,这引发了关于 Ccr4-Not 复合物在转录过程中作用的问题。在这里,我们明确证实 Ccr4-Not 是 RNA 聚合酶 II(RNAPII)的正向延伸因子。Ccr4-Not 复合物以类似于 RNAPII 的转录依赖性方式靶向基因的编码区,并在体内促进延伸。此外,Ccr4-Not 与延伸中的 RNAPII 复合物直接相互作用,并在体外刺激被阻遏的聚合酶的转录延伸。Ccr4-Not 可以使用不同于高度表征的延伸因子 TFIIS 的机制重新激活回退的 RNAPII。虽然 Ccr4-Not 与延伸复合物的相互作用不需要它,但它与正在延伸的转录本相互作用,并以依赖于转录本长度的方式促进延伸,尽管这种相互作用不是其结合 RNAPII 所必需的。我们的综合分析表明,Ccr4-Not 直接调节转录,并表明它通过在体内遇到转录障碍时促进被阻遏的 RNAPII 重新开始延伸来实现这一点。

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