<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Y</submitter><funding>Ministry of Science and Technology of China</funding><funding>USTC research funds</funding><funding>fundamental research funds for the central universities</funding><funding>National Natural Science Foundation of China</funding><pagination>20359</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8514580</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Previous studies indicated that the P-body components, CGH-1 and EDC-3 may play a crucial role in the regulation of lifespan in Caenorhabditis elegans. Homo sapiens DDX6 or Saccharomyces cerevisiae Dhh1p (CGH-1 in C. elegans) could form complexes with EDC3 (Edc3p in yeast), respectively, which is significant for translation inhibition and mRNA decay. However, it is currently unclear how CGH-1 can be recognized by EDC-3 in C. elegans. Here, we provided structural and biochemical insights into the interaction between CGH-1 and EDC-3. Combined with homology modeling, mutation, and ITC assays, we uncovered an interface between CGH-1 RecA2 domain and EDC-3 FDF-FEK. Additionally, GST-pulldown and co-localization experiments confirmed the interaction between CGH-1 and EDC-3 in vitro and in vivo. </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Insight into the interaction between the RNA helicase CGH-1 and EDC-3 and its implications.</pubmed_title><pmcid>PMC8514580</pmcid><funding_grant_id>31870760</funding_grant_id><funding_grant_id>WK2070000145</funding_grant_id><funding_grant_id>2019YFA0508403</funding_grant_id><funding_grant_id>31970669</funding_grant_id><funding_grant_id>KY2070000075</funding_grant_id><pubmed_authors>Yang K</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Hong J</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Insight into the interaction between the RNA helicase CGH-1 and EDC-3 and its implications.</name><description>Previous studies indicated that the P-body components, CGH-1 and EDC-3 may play a crucial role in the regulation of lifespan in Caenorhabditis elegans. Homo sapiens DDX6 or Saccharomyces cerevisiae Dhh1p (CGH-1 in C. elegans) could form complexes with EDC3 (Edc3p in yeast), respectively, which is significant for translation inhibition and mRNA decay. However, it is currently unclear how CGH-1 can be recognized by EDC-3 in C. elegans. Here, we provided structural and biochemical insights into the interaction between CGH-1 and EDC-3. Combined with homology modeling, mutation, and ITC assays, we uncovered an interface between CGH-1 RecA2 domain and EDC-3 FDF-FEK. Additionally, GST-pulldown and co-localization experiments confirmed the interaction between CGH-1 and EDC-3 in vitro and in vivo. </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-09T01:25:01.925Z</modification><creation>2022-02-11T12:10:31.722Z</creation></dates><accession>S-EPMC8514580</accession><cross_references><pubmed>34645931</pubmed><doi>10.1038/s41598-021-99919-0</doi></cross_references></HashMap>