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Suv420 enrichment at the centromere limits Aurora B localization and function.Suv420 在着丝粒处的富集限制了 Aurora B 的定位和功能。
J Cell Sci. 2021 Aug 1;134(15). doi: 10.1242/jcs.249763. Epub 2021 Aug 3.
2
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Int J Mol Sci. 2021 Apr 21;22(9):4309. doi: 10.3390/ijms22094309.
3
Centromeric transcription maintains centromeric cohesion in human cells.着丝粒转录维持人类细胞的着丝粒黏合。
J Cell Biol. 2021 Jul 5;220(7). doi: 10.1083/jcb.202008146.
4
The structure, function and evolution of a complete human chromosome 8.完整人类 8 号染色体的结构、功能与进化
Nature. 2021 May;593(7857):101-107. doi: 10.1038/s41586-021-03420-7. Epub 2021 Apr 7.
5
Cohesin: behind dynamic genome topology and gene expression reprogramming.黏连蛋白:动态基因组拓扑结构和基因表达重编程的背后。
Trends Cell Biol. 2021 Sep;31(9):760-773. doi: 10.1016/j.tcb.2021.03.005. Epub 2021 Mar 22.
6
Alpha-satellite RNA transcripts are repressed by centromere-nucleolus associations.α-卫星 RNA 转录本受着丝粒-核仁关联的抑制。
Elife. 2020 Nov 11;9:e59770. doi: 10.7554/eLife.59770.
7
ZFAT binds to centromeres to control noncoding RNA transcription through the KAT2B-H4K8ac-BRD4 axis.ZFAT 通过 KAT2B-H4K8ac-BRD4 轴与着丝粒结合来控制非编码 RNA 转录。
Nucleic Acids Res. 2020 Nov 4;48(19):10848-10866. doi: 10.1093/nar/gkaa815.
8
R-loop induced G-quadruplex in non-template promotes transcription by successive R-loop formation.非模板链上 R 环诱导的 G-四链体通过连续形成 R 环促进转录。
Nat Commun. 2020 Jul 7;11(1):3392. doi: 10.1038/s41467-020-17176-7.
9
Functioning mechanisms of Shugoshin-1 in centromeric cohesion during mitosis.Shugoshin-1 在有丝分裂中着丝粒黏合的作用机制。
Essays Biochem. 2020 Sep 4;64(2):289-297. doi: 10.1042/EBC20190077.
10
Cohesin Removal Reprograms Gene Expression upon Mitotic Entry.着丝粒蛋白复合物移除在有丝分裂起始时重编程基因表达。
Mol Cell. 2020 Apr 2;78(1):127-140.e7. doi: 10.1016/j.molcel.2020.01.023. Epub 2020 Feb 7.

转录在染色体分离中的新作用:持续的着丝粒转录维持着丝粒的黏合。

An emerging role of transcription in chromosome segregation: Ongoing centromeric transcription maintains centromeric cohesion.

机构信息

Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, 70112, USA.

Tulane Cancer Center, Tulane University School of Medicine, New Orleans, 70112, USA.

出版信息

Bioessays. 2022 Jan;44(1):e2100201. doi: 10.1002/bies.202100201. Epub 2021 Nov 10.

DOI:10.1002/bies.202100201
PMID:34761408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8958860/
Abstract

Non-coding centromeres, which dictate kinetochore formation for proper chromosome segregation, are extremely divergent in DNA sequences across species but are under active transcription carried out by RNA polymerase (RNAP) II. The RNAP II-mediated centromeric transcription has been shown to facilitate the deposition of the centromere protein A (CENP-A) to centromeres, establishing a conserved and critical role of centromeric transcription in centromere maintenance. Our recent work revealed another role of centromeric transcription in chromosome segregation: maintaining centromeric cohesion during mitosis. Interestingly, this role appears to be fulfilled through ongoing centromeric transcription rather than centromeric transcripts. In addition, we found that centromeric transcription may not require some of the traditional transcription initiation factors, suggestive of "uniqueness" in its regulation. In this review, we discuss the novel role and regulation of centromeric transcription as well as the potential underlying mechanisms.

摘要

非编码着丝粒在物种间的 DNA 序列上差异极大,但它们在功能上是高度保守的,对于染色体的正确分离起着关键作用。这些着丝粒通过 RNA 聚合酶 II(RNAP II)进行活跃的转录。研究表明,RNAP II 介导的着丝粒转录有助于将着丝粒蛋白 A(CENP-A)沉积到着丝粒上,从而确立了着丝粒转录在维持着丝粒功能中的保守和关键作用。我们最近的工作揭示了着丝粒转录在染色体分离中的另一个作用:在有丝分裂过程中维持着丝粒的黏合。有趣的是,这一作用似乎是通过持续的着丝粒转录而不是着丝粒转录本来实现的。此外,我们还发现,着丝粒转录可能不需要一些传统的转录起始因子,这表明其调控具有“独特性”。在这篇综述中,我们讨论了着丝粒转录的新作用和调控机制,以及潜在的潜在机制。

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