<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Treen N</submitter><funding>NHGRI</funding><funding>NHGRI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIH</funding><pagination>1150-1156.e4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5996753</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(7)</volume><pubmed_abstract>Most animal embryos display a delay in the activation of zygotic transcription during early embryogenesis [1]. This process is thought to help coordinate rapid increases in cell number during early development [2]. The timing of zygotic genome activation (ZGA) during the maternal-to-zygotic transition (MZT) remains uncertain despite extensive efforts. We explore ZGA in the simple protovertebrate, Ciona intestinalis. Single-cell RNA sequencing (RNA-seq) assays identified Cyclin B3 (Ccnb3) as a putative mediator of ZGA. Maternal Ccnb3 transcripts rapidly diminish in abundance during the onset of zygotic transcription at the 8-cell and 16-cell stages. Disruption of Ccnb3 activity results in precocious activation of zygotic transcription, while overexpression abolishes normal activation. These</pubmed_abstract><journal>Current biology : CB</journal><pubmed_title>Depletion of Maternal Cyclin B3 Contributes to Zygotic Genome Activation in the Ciona Embryo.</pubmed_title><pmcid>PMC5996753</pmcid><funding_grant_id>NS076542</funding_grant_id><funding_grant_id>T32HG003284</funding_grant_id><funding_grant_id>T32 HG003284</funding_grant_id><funding_grant_id>R01 NS076542</funding_grant_id><pubmed_authors>Levine M</pubmed_authors><pubmed_authors>Heist T</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Treen N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Depletion of Maternal Cyclin B3 Contributes to Zygotic Genome Activation in the Ciona Embryo.</name><description>Most animal embryos display a delay in the activation of zygotic transcription during early embryogenesis [1]. This process is thought to help coordinate rapid increases in cell number during early development [2]. The timing of zygotic genome activation (ZGA) during the maternal-to-zygotic transition (MZT) remains uncertain despite extensive efforts. We explore ZGA in the simple protovertebrate, Ciona intestinalis. Single-cell RNA sequencing (RNA-seq) assays identified Cyclin B3 (Ccnb3) as a putative mediator of ZGA. Maternal Ccnb3 transcripts rapidly diminish in abundance during the onset of zygotic transcription at the 8-cell and 16-cell stages. Disruption of Ccnb3 activity results in precocious activation of zygotic transcription, while overexpression abolishes normal activation. These</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2025-04-03T22:20:42.115Z</modification><creation>2019-08-04T08:11:39Z</creation></dates><accession>S-EPMC5996753</accession><cross_references><pubmed>29576477</pubmed><doi>10.1016/j.cub.2018.02.046</doi></cross_references></HashMap>