Complex human chromosomal and genomic rearrangements.

Complex human chromosomal and genomic rearrangements.
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DOI:
10.1016/j.tig.2009.05.005
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发表时间:
2009-07
期刊:
影响因子:
11.4
通讯作者:
Lupski, James R.
Lupski, James R.
中科院分区:
生物学1区
文献类型:
--
作者:
Zhang, Feng;Carvalho, Claudia M. B.;Lupski, James R.

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拷贝数变异(CNV)是人类遗传变异的主要来源。除了作为良性多态性存在之外,CNV还可以传递临床表型,包括基因组疾病、散发性疾病和复杂的人类性状。CNV由基因组重排引起,其可以代表基因组区段的简单缺失或重复,或者更复杂。复杂的染色体重排(CCR)已经知道了一段时间,但其机制仍然难以捉摸。最近的技术进步和高分辨率的人类基因组分析表明,复杂的基因组重排可以占很大一部分的非复发性重排在一个给定的基因座。各种机制,其中大部分是基于DNA复制,例如叉停滞和模板转换(FoSTeS)和微同源介导的断裂诱导复制(MMBIR),已被提出用于产生这种复杂的基因组重排,并可能负责CCR。
Copy number variation (CNV) is a major source of genetic variation among humans. In addition to existing as benign polymorphisms, CNVs can also convey clinical phenotypes, including genomic disorders, sporadic diseases and complex human traits. CNV results from genomic rearrangements that can represent simple deletion or duplication of a genomic segment, or be more complex. Complex chromosomal rearrangements (CCRs) have been known for some time but their mechanisms have remained elusive. Recent technology advances and high-resolution human genome analyses have revealed that complex genomic rearrangements can account for a large fraction of non-recurrent rearrangements at a given locus. Various mechanisms, most of which are DNA-replication-based, for example fork stalling and template switching (FoSTeS) and microhomology-mediated break-induced replication (MMBIR), have been proposed for generating such complex genomic rearrangements and are probably responsible for CCR.
DOI: 10.1016/j.ajhg.2007.11.002
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