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      What is an epigenetic transgenerational phenotype? F3 or F2.

      1
      Reproductive toxicology (Elmsford, N.Y.)
      Elsevier BV

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          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.

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          Author and article information

          Journal
          Reprod Toxicol
          Reproductive toxicology (Elmsford, N.Y.)
          Elsevier BV
          0890-6238
          0890-6238
          Jan 2008
          : 25
          : 1
          Affiliations
          [1 ] Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, WA 99164-4231, USA. skinner@mail.wsu.edu
          Article
          S0890-6238(07)00278-X NIHMS38687
          10.1016/j.reprotox.2007.09.001
          2249610
          17949945
          e6a4c59e-afa2-49dd-a79d-fe4da13b7c72
          History

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