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      Role of epigenetic transgenerational inheritance in generational toxicology

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          Abstract

          Many environmental toxicants have been shown to be associated with the transgenerational inheritance of increased disease susceptibility. This review describes the generational toxicity of some of these chemicals and their role in the induction of epigenetic transgenerational inheritance of disease. Epigenetic factors include DNA methylation, histone modifications, retention of histones in sperm, changes to chromatin structure, and expression of non-coding RNAs. For toxicant-induced epigenetic transgenerational inheritance to occur, exposure to a toxicant must result in epigenetic changes to germ cells (sperm or eggs) since it is the germ cells that carry molecular information to subsequent generations. In addition, the epigenetic changes induced in transgenerational generation animals must cause alterations in gene expression in these animals’ somatic cells. In some cases of generational toxicology, negligible changes are seen in the directly exposed generations, but increased disease rates are seen in transgenerational descendants. Governmental policies regulating toxicant exposure should take generational effects into account. A new approach that takes into consideration generational toxicity will be needed to protect our future populations.

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          Most cited references110

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          Gene expression regulation mediated through reversible m⁶A RNA methylation.

          Cellular RNAs carry diverse chemical modifications that used to be regarded as static and having minor roles in 'fine-tuning' structural and functional properties of RNAs. In this Review, we focus on reversible methylation through the most prevalent mammalian mRNA internal modification, N(6)-methyladenosine (m(6)A). Recent studies have discovered protein 'writers', 'erasers' and 'readers' of this RNA chemical mark, as well as its dynamic deposition on mRNA and other types of nuclear RNA. These findings strongly indicate dynamic regulatory roles that are analogous to the well-known reversible epigenetic modifications of DNA and histone proteins. This reversible RNA methylation adds a new dimension to the developing picture of post-transcriptional regulation of gene expression.
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            Sperm tsRNAs contribute to intergenerational inheritance of an acquired metabolic disorder.

            Increasing evidence indicates that metabolic disorders in offspring can result from the father's diet, but the mechanism remains unclear. In a paternal mouse model given a high-fat diet (HFD), we showed that a subset of sperm transfer RNA-derived small RNAs (tsRNAs), mainly from 5' transfer RNA halves and ranging in size from 30 to 34 nucleotides, exhibited changes in expression profiles and RNA modifications. Injection of sperm tsRNA fractions from HFD males into normal zygotes generated metabolic disorders in the F1 offspring and altered gene expression of metabolic pathways in early embryos and islets of F1 offspring, which was unrelated to DNA methylation at CpG-enriched regions. Hence, sperm tsRNAs represent a paternal epigenetic factor that may mediate intergenerational inheritance of diet-induced metabolic disorders.
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              RNA methylation by Dnmt2 protects transfer RNAs against stress-induced cleavage.

              Dnmt2 proteins are the most conserved members of the DNA methyltransferase enzyme family, but their substrate specificity and biological functions have been a subject of controversy. We show here that, in addition to tRNA(Asp-GTC), tRNA(Val-AAC) and tRNA(Gly-GCC) are also methylated by Dnmt2. Drosophila Dnmt2 mutants showed reduced viability under stress conditions, and Dnmt2 relocalized to stress granules following heat shock. Strikingly, stress-induced cleavage of tRNAs was Dnmt2-dependent, and Dnmt2-mediated methylation protected tRNAs against ribonuclease cleavage. These results uncover a novel biological function of Dnmt2-mediated tRNA methylation, and suggest a role for Dnmt2 enzymes during the biogenesis of tRNA-derived small RNAs.
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                Author and article information

                Contributors
                Journal
                Environ Epigenet
                Environ Epigenet
                eep
                Environmental Epigenetics
                Oxford University Press (UK )
                2058-5888
                2022
                16 February 2022
                16 February 2022
                : 8
                : 1 , Special Issue: Environmental Epigenetics and Generational Toxicology
                : dvac001
                Affiliations
                departmentCenter for Reproductive Biology, School of Biological Sciences, Washington State University , Pullman, WA 99164-4236, USA
                departmentCenter for Reproductive Biology, School of Biological Sciences, Washington State University , Pullman, WA 99164-4236, USA
                departmentCenter for Reproductive Biology, School of Biological Sciences, Washington State University , Pullman, WA 99164-4236, USA
                Author notes
                **Correspondence address. Center for Reproductive Biology, School of Biological Sciences, Washington State University, Pullman, WA 99164-4236, USA. Tel: +509-335-1524; E-mail: skinner@ 123456wsu.edu
                Author information
                https://orcid.org/0000-0001-8894-4054
                https://orcid.org/0000-0001-8224-2078
                Article
                dvac001
                10.1093/eep/dvac001
                8848501
                35186326
                e5d69456-83a6-4972-b480-326196ea2610
                © The Author(s) 2022. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 15 September 2021
                : 04 November 2021
                : 03 February 2022
                : 20 January 2022
                : 16 February 2022
                Page count
                Pages: 9
                Funding
                Funded by: John Templeton Foundation, DOI 10.13039/100000925;
                Award ID: 50183
                Funded by: John Templeton Foundation, DOI 10.13039/100000925;
                Award ID: 61174
                Categories
                Review Article
                AcademicSubjects/SCI02302

                epigenetics,generational toxicology,transgenerational

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