<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Boag PR</submitter><funding>NIGMS NIH HHS</funding><pagination>543-57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2500139</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>182(3)</volume><pubmed_abstract>During oogenesis, numerous messenger RNAs (mRNAs) are maintained in a translationally silenced state. In eukaryotic cells, various translation inhibition and mRNA degradation mechanisms congregate in cytoplasmic processing bodies (P bodies). The P body protein Dhh1 inhibits translation and promotes decapping-mediated mRNA decay together with Pat1 in yeast, and has been implicated in mRNA storage in metazoan oocytes. Here, we have investigated in Caenorhabditis elegans whether Dhh1 and Pat1 generally function together, and how they influence mRNA sequestration during oogenesis. We show that in somatic tissues, the Dhh1 orthologue (CGH-1) forms Pat1 (patr-1)-dependent P bodies that are involved in mRNA decapping. In contrast, during oogenesis, CGH-1 forms patr-1-independent mRNA storage bodi</pubmed_abstract><journal>The Journal of cell biology</journal><pubmed_title>Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis.</pubmed_title><pmcid>PMC2500139</pmcid><funding_grant_id>R01 GM063826</funding_grant_id><funding_grant_id>R01 GM065682</funding_grant_id><funding_grant_id>GM63826</funding_grant_id><funding_grant_id>GM65682</funding_grant_id><pubmed_authors>Robida S</pubmed_authors><pubmed_authors>Atalay A</pubmed_authors><pubmed_authors>Boag PR</pubmed_authors><pubmed_authors>Blackwell TK</pubmed_authors><pubmed_authors>Reinke V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis.</name><description>During oogenesis, numerous messenger RNAs (mRNAs) are maintained in a translationally silenced state. In eukaryotic cells, various translation inhibition and mRNA degradation mechanisms congregate in cytoplasmic processing bodies (P bodies). The P body protein Dhh1 inhibits translation and promotes decapping-mediated mRNA decay together with Pat1 in yeast, and has been implicated in mRNA storage in metazoan oocytes. Here, we have investigated in Caenorhabditis elegans whether Dhh1 and Pat1 generally function together, and how they influence mRNA sequestration during oogenesis. We show that in somatic tissues, the Dhh1 orthologue (CGH-1) forms Pat1 (patr-1)-dependent P bodies that are involved in mRNA decapping. In contrast, during oogenesis, CGH-1 forms patr-1-independent mRNA storage bodi</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Aug</publication><modification>2025-04-18T22:32:24.881Z</modification><creation>2019-03-27T00:16:06Z</creation></dates><accession>S-EPMC2500139</accession><cross_references><pubmed>18695045</pubmed><doi>10.1083/jcb.200801183</doi></cross_references></HashMap>