转录辅激活因子PGC-1α通过CBP80结合新合成的RNA: Co- and -转录后基因调控的纽带。

Xavier Rambout, Hana Cho, Lynne E Maquat
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引用次数: 4

摘要

哺乳动物细胞有许多质量控制机制来调节蛋白质编码基因的表达,以确保正确的转录物合成、加工和翻译。如果转录物代谢的一个步骤不能满足必要的空间、时间或结构标准,包括rna结合蛋白的适当获取,那么该步骤将停止,不能进行下一步,最终导致转录物降解。质量控制机制是一个连续的过程,从细胞核开始,延伸到细胞质。在这里,我们提供了已发表和未发表的蛋白质编码基因的数据,这些基因的表达被转录辅激活因子PGC-1α激活。我们发现PGC-1α从染色质(它被dna结合蛋白募集到染色质上)移动到新生转录物5'帽的CBP80上,开始了一系列共同和转录后的质量和数量控制步骤,总的来说,确保了适当的基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional Coactivator PGC-1α Binding to Newly Synthesized RNA via CBP80: A Nexus for Co- and Posttranscriptional Gene Regulation.

Mammalian cells have many quality-control mechanisms that regulate protein-coding gene expression to ensure proper transcript synthesis, processing, and translation. Should a step in transcript metabolism fail to fulfill requisite spatial, temporal, or structural criteria, including the proper acquisition of RNA-binding proteins, then that step will halt, fail to proceed to the next step, and ultimately result in transcript degradation. Quality-control mechanisms constitute a continuum of processes that initiate in the nucleus and extend to the cytoplasm. Here, we present published and unpublished data for protein-coding genes whose expression is activated by the transcriptional coactivator PGC-1α. We show that PGC-1α movement from chromatin, to which it is recruited by DNA-binding proteins, to CBP80 at the 5' cap of nascent transcripts begins a series of co- and posttranscriptional quality- and quantity-control steps that, in total, ensure proper gene expression.

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