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由不同的断裂诱导复制引起的涉及F8和FUNDC2的双重复杂突变。

Double complex mutations involving F8 and FUNDC2 caused by distinct break-induced replication.

作者信息

Sheen Campbell R, Jewell Ursula R, Morris Christine M, Brennan Stephen O, Férec Claude, George Peter M, Smith Mark P, Chen Jian-Min

机构信息

Molecular Pathology Laboratory, Canterbury Health Laboratories, Christchurch, New Zealand.

出版信息

Hum Mutat. 2007 Dec;28(12):1198-206. doi: 10.1002/humu.20591.

DOI:10.1002/humu.20591
PMID:17683067
Abstract

Genomic rearrangements are a well-recognized cause of genetic disease and can be formed by a variety of mechanisms. We report a complex rearrangement causing severe hemophilia A, identified and further characterized using a range of PCR-based methods, and confirmed using array-comparative genomic hybridization (array-CGH). This rearrangement consists of a 15.5-kb deletion/16-bp insertion located 0.6 kb from a 28.1-kb deletion/263-kb insertion at Xq28 and is one of the most complex rearrangements described at a DNA sequence level. We propose that the rearrangement was generated by distinct but linked cellular responses to double strand breakage, namely break-induced replication (BIR) and a novel model of break-induced serial replication slippage (SRS). The copy number of several genes is affected by this rearrangement, with deletion of part of the Factor VIII gene (F8, causing hemophilia A) and the FUNDC2 gene, and duplication of the TMEM185A, HSFX1, MAGEA9, and MAGEA11 genes. As the patient exhibits no clinically detectable phenotype other than hemophilia A, it appears that the biological effects of the other genes involved are not dosage-dependent. This investigation has provided novel insights into processes of DNA repair including BIR and the first description of SRS during repair in a pathological context.

摘要

基因组重排是一种公认的遗传疾病病因,可由多种机制形成。我们报告了一例导致严重甲型血友病的复杂重排,通过一系列基于聚合酶链反应(PCR)的方法进行鉴定和进一步表征,并使用阵列比较基因组杂交(array-CGH)进行确认。这种重排由位于Xq28处距一个28.1 kb缺失/263 kb插入0.6 kb处的一个15.5 kb缺失/16 bp插入组成,是在DNA序列水平上描述的最复杂的重排之一。我们提出,这种重排是由对双链断裂的不同但相关的细胞反应产生的,即断裂诱导复制(BIR)和一种新的断裂诱导序列复制滑移(SRS)模型。几个基因的拷贝数受这种重排影响,部分凝血因子VIII基因(F8,导致甲型血友病)和FUNDC2基因缺失,而TMEM185A、HSFX1、MAGEA9和MAGEA11基因发生重复。由于该患者除甲型血友病外无临床可检测到的表型,似乎所涉及的其他基因的生物学效应不依赖于剂量。这项研究为DNA修复过程提供了新的见解,包括BIR以及在病理背景下修复过程中SRS的首次描述。

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Hum Mutat. 2007 Dec;28(12):1198-206. doi: 10.1002/humu.20591.
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