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什么是表观遗传跨代表型?F3代还是F2代?

What is an epigenetic transgenerational phenotype? F3 or F2.

作者信息

Skinner Michael K

机构信息

Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, WA 99164-4231, USA.

出版信息

Reprod Toxicol. 2008 Jan;25(1):2-6. doi: 10.1016/j.reprotox.2007.09.001. Epub 2007 Sep 11.

Abstract

The ability of an environmental exposure to induce an epigenetic transgenerational adult onset disease phenotype is discussed in the current mini-review in the context of defining this phenomenon and the associated reproductive toxicology. A gestating female (F0 generation) exposure to an environmental compound results in the F1 generation embryo and F2 generation germ-line being directly exposed, such that the F3 generation is the first not directly exposed to the environmental compound. In contrast, postnatal or adult exposure (F0 generation) results in the F1 generation germ-line being exposed, such that F2 generation is the first to not be directly exposed to the environmental compound. The unequivocal transgenerational transmission of an adult onset disease phenotype through the germ-line requires assessment of the F3 generation for embryonic exposure, and F2 generation for postnatal exposure. This is in contrast to a number of F1 and F2 generation studies referred to as transgenerational. The reproductive toxicology associated with this transgenerational phenotype generally involves the reprogramming of the germ-line epigenome. The biological phenomenon involved in this reproductive toxicology deals with embryonic gonadal development and germ-line differentiation, or postnatally the gametogenesis process and germ cell development. The ability of an environmental compound (e.g. endocrine disruptor) to promote this reprogramming of the germ-line appears to be the causal factor in the epigenetic transgenerational phenotype.

摘要

在当前的小型综述中,在定义这种现象及相关生殖毒理学的背景下,讨论了环境暴露诱导表观遗传跨代成年发病疾病表型的能力。妊娠期雌性(F0代)暴露于环境化合物会导致F1代胚胎和F2代生殖系直接暴露,因此F3代是第一个未直接暴露于该环境化合物的世代。相比之下,出生后或成年期暴露(F0代)会导致F1代生殖系暴露,因此F2代是第一个未直接暴露于该环境化合物的世代。通过生殖系明确的成年发病疾病表型的跨代传递需要评估F3代的胚胎暴露情况以及F2代的出生后暴露情况。这与许多被称为跨代的F1和F2代研究形成对比。与这种跨代表型相关的生殖毒理学通常涉及生殖系表观基因组的重编程。这种生殖毒理学所涉及的生物学现象涉及胚胎性腺发育和生殖系分化,或者出生后的配子发生过程和生殖细胞发育。环境化合物(如内分泌干扰物)促进生殖系这种重编程的能力似乎是表观遗传跨代表型的因果因素。

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