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达成目的的新手段:mRNA 输出活性影响可变聚腺苷酸化。

New means to an end: mRNA export activity impacts alternative polyadenylation.

作者信息

Shin Jihae, Cheng Hong, Tian Bin

机构信息

Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, NJ, USA.

State Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, China.

出版信息

Transcription. 2019 Aug-Oct;10(4-5):207-211. doi: 10.1080/21541264.2019.1658557. Epub 2019 Sep 2.

Abstract

Gene expression involves multiple co- and post-transcriptional processes that have been increasingly found intertwined. A recent work by our groups (Chen et al. , 2019) indicates that expression of alternative polyadenylation isoforms in mammalian cells can be controlled by nuclear export activities. This regulation has distinct impacts on genes having different sizes and nucleotide contents, and involves RNA polymerase II distribution toward the 3' end of genes. This work raises a number of intriguing questions concerning how 3' end processing and nuclear export are integrated and how their regulation feeds back to transcription.

摘要

基因表达涉及多个转录共调控和转录后过程,人们越来越发现这些过程相互交织。我们团队最近的一项研究(Chen等人,2019年)表明,哺乳动物细胞中可变聚腺苷酸化异构体的表达可受核输出活性的控制。这种调控对具有不同大小和核苷酸含量的基因有不同影响,并且涉及RNA聚合酶II向基因3'端的分布。这项研究提出了许多有趣的问题,涉及3'端加工和核输出如何整合,以及它们的调控如何反馈到转录过程。

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本文引用的文献

2
A U2-snRNP-independent role of SF3b in promoting mRNA export.SF3b 在促进 mRNA 输出中的 U2-snRNP 非依赖性作用。
Proc Natl Acad Sci U S A. 2019 Apr 16;116(16):7837-7846. doi: 10.1073/pnas.1818835116. Epub 2019 Mar 28.

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