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R 环介导人类 rDNA 二级收缩的转录相关形成。

R-loops mediate transcription-associated formation of human rDNA secondary constrictions.

机构信息

Department of Genetics, College of Life Sciences, Wuhan University, Wuhan, China.

Department of Physiology, School of Basic medicine, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Cell Biochem. 2021 Oct;122(10):1517-1533. doi: 10.1002/jcb.30074. Epub 2021 Jul 5.

Abstract

The ribosomal gene DNA (rDNA) often forms secondary constrictions in the chromosome; however, the molecular mechanism involved remains poorly understood. Here, we report that occurrence of rDNA constriction was increased in the chromosomes in human cancer cell lines compared with normal cells and that decondensed rDNA was significantly enhanced after partial inhibition of rDNA transcription. rDNA transcription was found during the S phase when replication occurred, and thus, DNA replication inhibitors caused constriction formation through hindering rDNA transcription. Inhibition of ataxia ATR (telangiectasia-mutated and RAD3-related) induced rDNA constriction formation. Replication stress or transcription inhibition increased R-loop formation. Topoisomerase I and RNase H1 suppressed secondary constriction formation. These data demonstrate that transcription stress causes the accumulation of stable R-loops (RNA-DNA hybrid) and subsequent constriction formation in the chromosomes.

摘要

核糖体基因 DNA(rDNA)通常在染色体中形成二级缢痕;然而,相关的分子机制仍知之甚少。在这里,我们报告说,与正常细胞相比,人类癌细胞系中的染色体中 rDNA 缢痕的发生增加了,并且 rDNA 转录的部分抑制后去凝聚的 rDNA 明显增强。rDNA 转录发生在复制发生的 S 期,因此,DNA 复制抑制剂通过阻碍 rDNA 转录导致缢痕形成。ataxia ATR(毛细血管扩张性共济失调突变和 RAD3 相关)的抑制诱导 rDNA 缢痕形成。复制应激或转录抑制增加 R 环形成。拓扑异构酶 I 和 RNase H1 抑制二级缢痕形成。这些数据表明转录应激导致稳定的 R 环(RNA-DNA 杂交)的积累,并随后在染色体中形成缢痕。

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