Crosstalk between genetic and epigenetic information through cytosine deamination

被引:31
作者
Chahwan, Richard [1 ]
Wontakal, Sandeep N. [1 ]
Roa, Sergio [1 ]
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
关键词
INDUCED CYTIDINE DEAMINASE; SINGLE-STRANDED-DNA; RNA EDITING ENZYME; SOMATIC HYPERMUTATION; ANTIBODY DIVERSIFICATION; B-CELLS; AID/APOBEC FAMILY; DRUG-RESISTANCE; PATERNAL GENOME; AID DEFICIENCY;
D O I
10.1016/j.tig.2010.07.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Decades of work have elucidated the existence of two forms of heritable information, namely genetic and epigenetic, which are collectively referred to as the 'dual inheritance'. The underlying mechanisms behind these two modes of inheritance have so far remained distinct. Cytosine deaminases, such as activation-induced cytidine deaminase (AID) and other members of the APOBEC family, have been implicated both in genetic variation of somatic cells and in epigenetic remodeling of germ and pluripotent cells. We hereby synthesize these seemingly dissociated functions into one coherent model, and further suggest that cytosine deaminases, particularly AID, might have a broader influence by modulating epigenetic information in somatic or cancer cells, as well as by triggering genetic variation in germ and pluripotent cells through mutation followed by natural selection. We therefore propose that the AID/APOBEC family of deaminases are likely to have acted as drivers throughout vertebrate evolution.
引用
收藏
页码:443 / 448
页数:6
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