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GU 丰富元件和 CELF1 对 mRNA 降解网络的协调调控。

Coordinate regulation of mRNA decay networks by GU-rich elements and CELF1.

机构信息

Department of Microbiology, Center for Infectious Diseases and Microbiology Translational Research, University of Minnesota, Minneapolis, MN, USA.

出版信息

Curr Opin Genet Dev. 2011 Aug;21(4):444-51. doi: 10.1016/j.gde.2011.03.002. Epub 2011 Apr 13.

Abstract

The GU-rich element (GRE) was identified as a conserved sequence enriched in the 3' UTR of human transcripts that exhibited rapid mRNA turnover. In mammalian cells, binding to GREs by the protein CELF1 coordinates mRNA decay of networks of transcripts involved in cell growth, migration, and apoptosis. Depending on the context, GREs and CELF1 also regulate pre-mRNA splicing and translation. GREs are highly conserved throughout evolution and play important roles in the development of organisms ranging from worms to man. In humans, abnormal GRE-mediated regulation contributes to disease states and cancer. Thus, GREs and CELF proteins serve critical functions in gene expression regulation and define an important evolutionarily conserved posttranscriptional regulatory network.

摘要

富含 GU 的元件 (GRE) 被鉴定为富含人类转录本 3'UTR 的保守序列,这些转录本表现出快速的 mRNA 周转。在哺乳动物细胞中,蛋白 CELF1 与 GRE 的结合协调了参与细胞生长、迁移和凋亡的转录本网络的 mRNA 降解。根据具体情况,GRE 和 CELF1 还调节前体 mRNA 的剪接和翻译。GRE 在整个进化过程中高度保守,在从蠕虫到人类的生物体的发育中发挥着重要作用。在人类中,异常的 GRE 介导的调节导致疾病状态和癌症。因此,GRE 和 CELF 蛋白在基因表达调控中发挥着关键作用,并定义了一个重要的进化上保守的转录后调控网络。

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