Genetic Diversification by Somatic Gene Conversion

被引:22
|
作者
Kurosawa, Kohei [1 ]
Ohta, Kunihiro [1 ]
机构
[1] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan
关键词
immunoglobulin locus; gene conversion; DNA break; recombination; INDUCED CYTIDINE DEAMINASE; LIGHT-CHAIN GENE; DOUBLE-STRAND BREAKS; B-CELL; HISTONE ACETYLATION; ANTIBODY REPERTOIRE; AID; RECOMBINATION; DNA; TRANSCRIPTION;
D O I
10.3390/genes2010048
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene conversion is a type of homologous recombination that leads to transfer of genetic information among homologous DNA sequences. It can be categorized into two classes: homogenizing and diversifying gene conversions. The former class results in neutralization and homogenization of any sequence variation among repetitive DNA sequences, and thus is important for concerted evolution. On the other hand, the latter functions to increase genetic diversity at the recombination-recipient loci. Thus, these two types of gene conversion play opposite roles in genome dynamics. Diversifying gene conversion is observed in the immunoglobulin (Ig) loci of chicken, rabbit, and other animals, and directs the diversification of Ig variable segments and acquisition of functional Ig repertoires. This type of gene conversion is initiated by the biased occurrence of recombination initiation events (e.g., DNA single-or double-strand breaks) on the recipient DNA site followed by unidirectional homologous recombination from multiple template sequences. Transcription and DNA accessibility is also important in the regulation of biased recombination initiation. In this review, we will discuss the biological significance and possible mechanisms of diversifying gene conversion in somatic cells of eukaryotes.
引用
收藏
页码:48 / 58
页数:11
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