<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ortega MA</submitter><funding>NICHD NIH HHS</funding><funding>National Institutes of Health</funding><pagination>1806-12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4909515</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>117(8)</volume><pubmed_abstract>After fertilization, the maternal and paternal chromosomes independently proceed through pronuclear formation. These chromatin reconfigurations occur within a shared cytoplasm thus exposing both gametes to the same factors. Here, we report that continuous cycloheximide [40 μg/mL] treatment of parthenogenotes, androgenotes, and ICSI embryos reveals ORC2 pronuclear instability in the maternal (MPN) but not the paternal pronucleus (PPN). When released from CHX after 8 h, the MPN can recover ORC2 and proceed through replication, however, parthenogenotes encounter severe mitotic defects while both ICSI embryos and androgenotes are able to recover and develop at significantly higher rates. Taken together, these data suggest cycloheximide treatment promotes an environment that asymmetrically affe</pubmed_abstract><journal>Journal of cellular biochemistry</journal><pubmed_title>Presence of the Paternal Pronucleus Assists Embryo in Overcoming Cycloheximide Induced Abnormalities in Zygotic Mitosis.</pubmed_title><pmcid>PMC4909515</pmcid><funding_grant_id>HD060722</funding_grant_id><funding_grant_id>R01 HD028501</funding_grant_id><funding_grant_id>R01 HD060722</funding_grant_id><pubmed_authors>Oshiro M</pubmed_authors><pubmed_authors>Ko M</pubmed_authors><pubmed_authors>Marh J</pubmed_authors><pubmed_authors>Ward WS</pubmed_authors><pubmed_authors>Finberg A</pubmed_authors><pubmed_authors>Ortega MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Presence of the Paternal Pronucleus Assists Embryo in Overcoming Cycloheximide Induced Abnormalities in Zygotic Mitosis.</name><description>After fertilization, the maternal and paternal chromosomes independently proceed through pronuclear formation. These chromatin reconfigurations occur within a shared cytoplasm thus exposing both gametes to the same factors. Here, we report that continuous cycloheximide [40 μg/mL] treatment of parthenogenotes, androgenotes, and ICSI embryos reveals ORC2 pronuclear instability in the maternal (MPN) but not the paternal pronucleus (PPN). When released from CHX after 8 h, the MPN can recover ORC2 and proceed through replication, however, parthenogenotes encounter severe mitotic defects while both ICSI embryos and androgenotes are able to recover and develop at significantly higher rates. Taken together, these data suggest cycloheximide treatment promotes an environment that asymmetrically affe</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2025-04-19T15:02:35.086Z</modification><creation>2019-03-27T02:16:09Z</creation></dates><accession>S-EPMC4909515</accession><cross_references><pubmed>26729559</pubmed><doi>10.1002/jcb.25480</doi></cross_references></HashMap>