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XRN2 Links Transcription Termination to DNA Damage and Replication Stress.XRN2 将转录终止与 DNA 损伤和复制应激联系起来。
PLoS Genet. 2016 Jul 20;12(7):e1006107. doi: 10.1371/journal.pgen.1006107. eCollection 2016 Jul.
2
Prevalent, Dynamic, and Conserved R-Loop Structures Associate with Specific Epigenomic Signatures in Mammals.普遍存在、动态变化且保守的R环结构与哺乳动物特定的表观基因组特征相关。
Mol Cell. 2016 Jul 7;63(1):167-78. doi: 10.1016/j.molcel.2016.05.032. Epub 2016 Jun 30.
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S1-DRIP-seq identifies high expression and polyA tracts as major contributors to R-loop formation.S1-DRIP-seq鉴定出高表达和多聚腺苷酸序列是R环形成的主要促成因素。
Genes Dev. 2016 Jun 1;30(11):1327-38. doi: 10.1101/gad.280834.116.
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Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci.筛查与 ALS 和额颞叶痴呆相关的基因座上新的六核苷酸重复扩展。
Neurol Genet. 2016 May 11;2(3):e71. doi: 10.1212/NXG.0000000000000071. eCollection 2016 Jun.
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Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.C9ORF72缺失会损害自噬,并与多聚谷氨酰胺Ataxin-2协同作用,导致运动神经元功能障碍和细胞死亡。
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The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription.范可尼贫血通路通过协调复制和转录来维持基因组稳定性。
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The Fanconi Anemia Pathway Protects Genome Integrity from R-loops.范可尼贫血通路保护基因组完整性免受R环影响。
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8
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R环与人类疾病的关联

R Loops and Links to Human Disease.

作者信息

Richard Patricia, Manley James L

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

J Mol Biol. 2017 Oct 27;429(21):3168-3180. doi: 10.1016/j.jmb.2016.08.031. Epub 2016 Sep 4.

DOI:10.1016/j.jmb.2016.08.031
PMID:27600412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5478472/
Abstract

Aberrant R-loop structures are increasingly being realized as an important contributor to human disease. R loops, which are mainly co-transcriptional, abundant RNA/DNA hybrids, form naturally and can indeed be beneficial for transcription regulation at certain loci. However, their unwanted persistence elsewhere or in particular situations can lead to DNA double-strand breaks, chromosome rearrangements, and hypermutation, which are all sources of genomic instability. Mutations in genes involved in R-loop resolution or mutations leading to R-loop formation at specific genes affect the normal physiology of the cell. We discuss here the examples of diseases for which a link with R loops has been described, as well as how disease-causing mutations might participate in the development and/or progression of diseases that include repeat-associated conditions, other neurological disorders, and cancers.

摘要

异常的R环结构日益被认为是导致人类疾病的一个重要因素。R环主要是共转录的、丰富的RNA/DNA杂交体,自然形成,并且在某些位点确实有利于转录调控。然而,它们在其他地方或特定情况下的异常持续存在会导致DNA双链断裂、染色体重排和超突变,这些都是基因组不稳定的来源。参与R环解决的基因突变或导致特定基因形成R环的突变会影响细胞的正常生理功能。我们在此讨论已描述与R环相关的疾病实例,以及致病突变可能如何参与包括重复相关疾病、其他神经疾病和癌症在内的疾病的发生和/或进展。