Biparental contributions of the H2A.B histone variant control embryonic development in mice
AffiliationDepartment of Cellular and Molecular Medicine, University of Arizona
MetadataShow full item record
PublisherPublic Library of Science
CitationMolaro A, Wood AJ, Janssens D, Kindelay SM, Eickbush MT, Wu S, et al. (2020) Biparental contributions of the H2A.B histone variant control embryonic development in mice. PLoS Biol 18(12): e3001001.
RightsCopyright © 2020 Molaro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License.
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AbstractHistone variants expand chromatin functions in eukaryote genomes. H2A.B genes are testis-expressed short histone H2A variants that arose in placental mammals. Their biological functions remain largely unknown. To investigate their function, we generated a knockout (KO) model that disrupts all 3 H2A.B genes in mice. We show that H2A.B KO males have globally altered chromatin structure in postmeiotic germ cells. Yet, they do not show impaired spermatogenesis or testis function. Instead, we find that H2A.B plays a crucial role postfertilization. Crosses between H2A.B KO males and females yield embryos with lower viability and reduced size. Using a series of genetic crosses that separate parental and zygotic contributions, we show that the H2A.B status of both the father and mother, but not of the zygote, affects embryonic viability and growth during gestation. We conclude that H2A.B is a novel parental-effect gene, establishing a role for short H2A histone variants in mammalian development. We posit that parental antagonism over embryonic growth drove the origin and ongoing diversification of short histone H2A variants in placental mammals. Copyright: © 2020 Molaro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Except where otherwise noted, this item's license is described as Copyright © 2020 Molaro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License.
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