<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4</volume><submitter>Kelley M</submitter><funding>American Cancer Society</funding><funding>NIBIB NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>National Institutes of Health (NIH)</funding><funding>National Marfan Foundation (NMF)</funding><funding>NINDS NIH HHS</funding><funding>Human Frontier Science Program (HFSP)</funding><funding>Fondo Nacional de Desarrollo Científico y Tecnológico</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>During development, biomechanical forces contour the body and provide shape to internal organs. Using genetic and molecular approaches in combination with a FRET-based tension sensor, we characterized a pulling force exerted by the elongating pharynx (foregut) on the anterior epidermis during C. elegans embryogenesis. Resistance of the epidermis to this force and to actomyosin-based circumferential constricting forces is mediated by FBN-1, a ZP domain protein related to vertebrate fibrillins. fbn-1 was required specifically within the epidermis and FBN-1 was expressed in epidermal cells and secreted to the apical surface as a putative component of the embryonic sheath. Tiling array studies indicated that fbn-1 mRNA processing requires the conserved alternative splicing factor MEC-8/RBPMS. </pubmed_abstract><journal>eLife</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4395870</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>FBN-1, a fibrillin-related protein, is required for resistance of the epidermis to mechanical deformation during C. elegans embryogenesis.</pubmed_title><pmcid>PMC4395870</pmcid><funding_grant_id>NS073121</funding_grant_id><funding_grant_id>1131038</funding_grant_id><funding_grant_id>R01 GM108754</funding_grant_id><funding_grant_id>S10RR02557401</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><funding_grant_id>Long-Term Fellowship</funding_grant_id><funding_grant_id>GM108754</funding_grant_id><funding_grant_id>NS047715</funding_grant_id><funding_grant_id>EB006745</funding_grant_id><funding_grant_id>1K99NS089942-01</funding_grant_id><funding_grant_id>R01 NS064273</funding_grant_id><funding_grant_id>R01 GM066868</funding_grant_id><funding_grant_id>GM30997</funding_grant_id><funding_grant_id>RSG-12-149-01-DCC</funding_grant_id><funding_grant_id>R37 GM030997</funding_grant_id><funding_grant_id>K99 NS089942</funding_grant_id><funding_grant_id>P20 GM103432</funding_grant_id><funding_grant_id>R01 EB006745</funding_grant_id><funding_grant_id>R01 GM030997</funding_grant_id><funding_grant_id>R01 NS073121</funding_grant_id><funding_grant_id>GM066868</funding_grant_id><funding_grant_id>NS064273</funding_grant_id><funding_grant_id>R01 NS047715</funding_grant_id><pubmed_authors>Fay DS</pubmed_authors><pubmed_authors>Kelley M</pubmed_authors><pubmed_authors>Heiman MG</pubmed_authors><pubmed_authors>Krieg M</pubmed_authors><pubmed_authors>Calixto A</pubmed_authors><pubmed_authors>Chalfie M</pubmed_authors><pubmed_authors>Yochem J</pubmed_authors><pubmed_authors>Kuzmanov A</pubmed_authors><pubmed_authors>Frand A</pubmed_authors><pubmed_authors>Meli V</pubmed_authors><pubmed_authors>Goodman MB</pubmed_authors><pubmed_authors>Shaham S</pubmed_authors></additional><is_claimable>false</is_claimable><name>FBN-1, a fibrillin-related protein, is required for resistance of the epidermis to mechanical deformation during C. elegans embryogenesis.</name><description>During development, biomechanical forces contour the body and provide shape to internal organs. Using genetic and molecular approaches in combination with a FRET-based tension sensor, we characterized a pulling force exerted by the elongating pharynx (foregut) on the anterior epidermis during C. elegans embryogenesis. Resistance of the epidermis to this force and to actomyosin-based circumferential constricting forces is mediated by FBN-1, a ZP domain protein related to vertebrate fibrillins. fbn-1 was required specifically within the epidermis and FBN-1 was expressed in epidermal cells and secreted to the apical surface as a putative component of the embryonic sheath. Tiling array studies indicated that fbn-1 mRNA processing requires the conserved alternative splicing factor MEC-8/RBPMS. </description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Mar</publication><modification>2026-05-07T22:02:01.356Z</modification><creation>2025-06-01T00:10:00.833Z</creation></dates><accession>S-EPMC4395870</accession><cross_references><pubmed>25798732</pubmed><doi>10.7554/eLife.06565</doi></cross_references></HashMap>