Gene Conversion in Human Genetic Disease

被引:13
|
作者
Chen, Jian-Min [1 ,2 ,3 ]
Ferec, Claude [1 ,2 ,3 ,4 ]
Cooper, David N. [5 ]
机构
[1] INSERM U613, F-29218 Brest, France
[2] EFS Bretagne, Brest, France
[3] Univ Bretagne Occidentale, Fac Med & Sci Sante, Brest, France
[4] Hop Morvan, CHU Brest, Lab Genet Mol & Histocompatibili, Brest, France
[5] Cardiff Univ, Sch Med, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales
关键词
gene conversion mutation; homologous recombination; human inherited disease; B DNA CONFORMATIONS; MULTIPLE MUTATIONS; INHERITED DISEASE; RECOMBINATION; EVENTS; DIVERSITY; SEQUENCES; EXCHANGE; HOTSPOT; ALLELE;
D O I
10.3390/genes1030550
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene conversion is a specific type of homologous recombination that involves the unidirectional transfer of genetic material from a 'donor' sequence to a highly homologous 'acceptor'. We have recently reviewed the molecular mechanisms underlying gene conversion, explored the key part that this process has played in fashioning extant human genes, and performed a meta-analysis of gene-conversion events known to have caused human genetic disease. Here we shall briefly summarize some of the latest developments in the study of pathogenic gene conversion events, including (i) the emerging idea of minimal efficient sequence homology (MESH) for homologous recombination, (ii) the local DNA sequence features that appear to predispose to gene conversion, (iii) a mechanistic comparison of gene conversion and transient hypermutability, and (iv) recently reported examples of pathogenic gene conversion events.
引用
收藏
页码:550 / 563
页数:14
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