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通过胞嘧啶脱氨酶实现遗传信息与表观遗传信息的串扰。

Crosstalk between genetic and epigenetic information through cytosine deamination.

机构信息

Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Trends Genet. 2010 Oct;26(10):443-8. doi: 10.1016/j.tig.2010.07.005. Epub 2010 Aug 26.

Abstract

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.

摘要

几十年来的研究已经阐明了存在两种形式的可遗传信息,即遗传和表观遗传,它们统称为“双重遗传”。这两种遗传模式的潜在机制迄今为止仍然截然不同。胞嘧啶脱氨酶,如激活诱导的胞嘧啶脱氨酶(AID)和 APOBEC 家族的其他成员,不仅与体细胞的遗传变异有关,而且与生殖细胞和多能细胞的表观遗传重塑有关。我们在此将这些看似分离的功能综合成一个连贯的模型,并进一步提出,胞嘧啶脱氨酶,特别是 AID,可能通过调节体细胞或癌细胞中的表观遗传信息,以及通过突变后自然选择在生殖细胞和多能细胞中引发遗传变异,从而产生更广泛的影响。因此,我们提出 AID/APOBEC 家族的脱氨酶可能在整个脊椎动物进化过程中充当了驱动因素。

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