<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Iqbal K</submitter><funding>NIEHS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>59</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4376074</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Exposure to environmental endocrine-disrupting chemicals during pregnancy reportedly causes transgenerationally inherited reproductive defects. We hypothesized that to affect the grandchild, endocrine-disrupting chemicals must alter the epigenome of the germ cells of the in utero-exposed G1 male fetus. Additionally, to affect the great-grandchild, the aberration must persist in the germ cells of the unexposed G2 grandchild.&lt;h4>Results&lt;/h4>Here, we treat gestating female mice with vinclozolin, bisphenol A, or di-(2-ethylhexyl)phthalate during the time when global de novo DNA methylation and imprint establishment occurs in the germ cells of the G1 male fetus. We map genome-wide features in purified G1 and G2 prospermatogonia, in order to detect immediate and persistent epi</pubmed_abstract><journal>Genome biology</journal><pubmed_title>Deleterious effects of endocrine disruptors are corrected in the mammalian germline by epigenome reprogramming.</pubmed_title><pmcid>PMC4376074</pmcid><funding_grant_id>R01ES015185</funding_grant_id><funding_grant_id>R01GM064378</funding_grant_id><funding_grant_id>P30 CA033572</funding_grant_id><funding_grant_id>R01 ES015185</funding_grant_id><funding_grant_id>R01 GM064378</funding_grant_id><pubmed_authors>Warden C</pubmed_authors><pubmed_authors>Li AX</pubmed_authors><pubmed_authors>Bai AY</pubmed_authors><pubmed_authors>Singh P</pubmed_authors><pubmed_authors>Szabo PE</pubmed_authors><pubmed_authors>Iqbal K</pubmed_authors><pubmed_authors>Pfeifer GP</pubmed_authors><pubmed_authors>Tran DA</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deleterious effects of endocrine disruptors are corrected in the mammalian germline by epigenome reprogramming.</name><description>&lt;h4>Background&lt;/h4>Exposure to environmental endocrine-disrupting chemicals during pregnancy reportedly causes transgenerationally inherited reproductive defects. We hypothesized that to affect the grandchild, endocrine-disrupting chemicals must alter the epigenome of the germ cells of the in utero-exposed G1 male fetus. Additionally, to affect the great-grandchild, the aberration must persist in the germ cells of the unexposed G2 grandchild.&lt;h4>Results&lt;/h4>Here, we treat gestating female mice with vinclozolin, bisphenol A, or di-(2-ethylhexyl)phthalate during the time when global de novo DNA methylation and imprint establishment occurs in the germ cells of the G1 male fetus. We map genome-wide features in purified G1 and G2 prospermatogonia, in order to detect immediate and persistent epi</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Mar</publication><modification>2026-06-14T05:26:11.857Z</modification><creation>2026-06-14T03:09:26.882Z</creation></dates><accession>S-EPMC4376074</accession><cross_references><pubmed>25853433</pubmed><doi>10.1186/s13059-015-0619-z</doi></cross_references></HashMap>