<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cheng E</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Fonds de recherche du Québec – Nature et technologies</funding><funding>NIH HHS</funding><pagination>e1011351</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11706408</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(12)</volume><pubmed_abstract>Stem and progenitor cell mitosis is essential for tissue development and homeostasis. How these cells ensure proper chromosome segregation, and thereby maintain mitotic fidelity, in the complex physiological environment of a living animal is poorly understood. Here we use in situ live-cell imaging of C. elegans germline stem and progenitor cells (GSPCs) to ask how the signaling environment influences stem and progenitor cell mitosis in vivo. Through a candidate screen we identify a new role for the insulin/IGF receptor (IGFR), daf-2, during GSPC mitosis. Mitosis is delayed in daf-2/IGFR mutants, and these delays require canonical, DAF-2/IGFR to DAF-16/FoxO insulin signaling, here acting cell non-autonomously from the soma. Interestingly, mitotic delays in daf-2/IGFR mutants depend on the s</pubmed_abstract><journal>PLoS genetics</journal><pubmed_title>Non-autonomous insulin signaling delays mitotic progression in C. elegans germline stem and progenitor cells.</pubmed_title><pmcid>PMC11706408</pmcid><funding_grant_id>RGPIN/05199-2020</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><funding_grant_id>283252</funding_grant_id><pubmed_authors>Cheng E</pubmed_authors><pubmed_authors>Gerhold AR</pubmed_authors><pubmed_authors>Lu R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Non-autonomous insulin signaling delays mitotic progression in C. elegans germline stem and progenitor cells.</name><description>Stem and progenitor cell mitosis is essential for tissue development and homeostasis. How these cells ensure proper chromosome segregation, and thereby maintain mitotic fidelity, in the complex physiological environment of a living animal is poorly understood. Here we use in situ live-cell imaging of C. elegans germline stem and progenitor cells (GSPCs) to ask how the signaling environment influences stem and progenitor cell mitosis in vivo. Through a candidate screen we identify a new role for the insulin/IGF receptor (IGFR), daf-2, during GSPC mitosis. Mitosis is delayed in daf-2/IGFR mutants, and these delays require canonical, DAF-2/IGFR to DAF-16/FoxO insulin signaling, here acting cell non-autonomously from the soma. Interestingly, mitotic delays in daf-2/IGFR mutants depend on the s</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-05-29T15:22:52.544Z</modification><creation>2025-04-04T21:49:29.543Z</creation></dates><accession>S-EPMC11706408</accession><cross_references><pubmed>39715269</pubmed><doi>10.1371/journal.pgen.1011351</doi></cross_references></HashMap>