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多亚基 CCR4-NOT 脱腺苷酸酶在 mRNA 降解起始中的调控。

Regulation of the multisubunit CCR4-NOT deadenylase in the initiation of mRNA degradation.

机构信息

Department of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.

RNA Biology Laboratory & Center for Structural Biology, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702-1201, USA.

出版信息

Curr Opin Struct Biol. 2022 Dec;77:102460. doi: 10.1016/j.sbi.2022.102460. Epub 2022 Sep 16.

Abstract

The conserved CCR4-NOT complex initiates the decay of mRNAs by catalyzing the shortening of their poly(A) tails in a process known as deadenylation. Recent studies have provided mechanistic insights into the action and regulation of this molecular machine. The two catalytic enzymatic subunits of the complex hydrolyze polyadenosine RNA. Notably, the non-catalytic subunits substantially enhance the complex's affinity and sequence selectivity for polyadenosine by directly contacting the RNA. An additional regulatory mechanism is the active recruitment of the CCR4-NOT to transcripts targeted for decay by RNA-binding proteins that recognize motifs or sequences residing predominantly in untranslated regions. This targeting and strict control of the mRNA deadenylation process emerges as a crucial nexus during post-transcriptional regulation of gene expression.

摘要

保守的 CCR4-NOT 复合物通过催化其 poly(A) 尾巴缩短来启动 mRNA 的降解,这个过程被称为去腺苷酸化。最近的研究提供了对这种分子机器的作用和调节的机制见解。该复合物的两个催化酶亚基水解多腺苷酸 RNA。值得注意的是,非催化亚基通过直接与 RNA 结合,大大提高了复合物对多腺苷酸的亲和力和序列选择性。另一个调节机制是通过识别主要位于非翻译区的基序或序列的 RNA 结合蛋白将 CCR4-NOT 复合物主动募集到靶向降解的转录本。这种靶向和严格控制 mRNA 去腺苷酸化过程成为转录后基因表达调控的关键枢纽。

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