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核仁 DNA 双链断裂反应是 rDNA 基因组稳定性的基础。

Nucleolar DNA Double-Strand Break Responses Underpinning rDNA Genomic Stability.

机构信息

Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland Galway, Galway, Ireland.

Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland Galway, Galway, Ireland.

出版信息

Trends Genet. 2019 Oct;35(10):743-753. doi: 10.1016/j.tig.2019.07.001. Epub 2019 Jul 25.

Abstract

Nucleoli, the sites of ribosome biogenesis, form around ribosomal gene (rDNA) arrays termed nucleolar organiser regions (NORs). These are the most transcriptionally active regions of the human genome and specialised responses have evolved to ensure their genomic stability. This review focuses on nucleolar responses to DNA double-strand breaks (DSBs) introduced into rDNA arrays using sequence-specific endonucleases, including CRISPR/Cas9. Repair of rDNA DSBs is predominantly carried out by the homology-directed repair (HDR) pathway that is facilitated by inhibition of transcription by RNA polymerase-I (Pol-I) and ensuing dramatic nucleolar reorganisation. Additionally, we review evidence that nucleoli can sense and respond to DSBs elsewhere in the genome.

摘要

核仁是核糖体生物发生的部位,围绕着核糖体基因(rDNA)阵列形成,这些阵列被称为核仁组织者区域(NORs)。这些是人类基因组中转录最活跃的区域,已经进化出了专门的反应来确保它们的基因组稳定性。这篇综述的重点是核仁对使用序列特异性内切酶(包括 CRISPR/Cas9)引入 rDNA 阵列中的 DNA 双链断裂(DSB)的反应。rDNA DSB 的修复主要是通过同源定向修复(HDR)途径进行的,该途径通过 RNA 聚合酶-I(Pol-I)转录抑制和随后的剧烈核仁重排来促进。此外,我们还回顾了核仁可以感知和响应基因组其他部位 DSB 的证据。

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