Department of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Genes Dev. 2011 Mar 15;25(6):581-93. doi: 10.1101/gad.2020911.
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.
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。