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CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans

The onset of sexual maturity involves dramatic changes in physiology and gene expression in many animals. These include abundant yolk protein production in egg-laying species, an energetically costly process under extensive transcriptional control. Here, we used the model organism Caenorhabditis ele...

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Autores principales: Van de Walle, Pieter, Geens, Ellen, Baggerman, Geert, José Naranjo-Galindo, Francisco, Askjaer, Peter, Schoofs, Liliane, Temmerman, Liesbet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824563/
https://www.ncbi.nlm.nih.gov/pubmed/31675356
http://dx.doi.org/10.1371/journal.pbio.3000499
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author Van de Walle, Pieter
Geens, Ellen
Baggerman, Geert
José Naranjo-Galindo, Francisco
Askjaer, Peter
Schoofs, Liliane
Temmerman, Liesbet
author_facet Van de Walle, Pieter
Geens, Ellen
Baggerman, Geert
José Naranjo-Galindo, Francisco
Askjaer, Peter
Schoofs, Liliane
Temmerman, Liesbet
author_sort Van de Walle, Pieter
collection PubMed
description The onset of sexual maturity involves dramatic changes in physiology and gene expression in many animals. These include abundant yolk protein production in egg-laying species, an energetically costly process under extensive transcriptional control. Here, we used the model organism Caenorhabditis elegans to provide evidence for the spatiotemporally defined interaction of two evolutionarily conserved transcription factors, CEH-60/PBX and UNC-62/MEIS, acting as a gateway to yolk protein production. Via proteomics, bimolecular fluorescence complementation (BiFC), and biochemical and functional readouts, we show that this interaction occurs in the intestine of animals at the onset of sexual maturity and suffices to support the reproductive program. Our electron micrographs and functional assays provide evidence that intestinal PBX/MEIS cooperation drives another process that depends on lipid mobilization: the formation of an impermeable epicuticle. Without this lipid-rich protective layer, mutant animals are hypersensitive to exogenous oxidative stress and are poor partners for mating. Dedicated communication between the hypodermis and intestine in C. elegans likely supports these physiological outcomes, and we propose a fundamental role for the conserved PBX/MEIS interaction in multicellular signaling networks that rely on lipid homeostasis.
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spelling pubmed-68245632019-11-12 CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans Van de Walle, Pieter Geens, Ellen Baggerman, Geert José Naranjo-Galindo, Francisco Askjaer, Peter Schoofs, Liliane Temmerman, Liesbet PLoS Biol Research Article The onset of sexual maturity involves dramatic changes in physiology and gene expression in many animals. These include abundant yolk protein production in egg-laying species, an energetically costly process under extensive transcriptional control. Here, we used the model organism Caenorhabditis elegans to provide evidence for the spatiotemporally defined interaction of two evolutionarily conserved transcription factors, CEH-60/PBX and UNC-62/MEIS, acting as a gateway to yolk protein production. Via proteomics, bimolecular fluorescence complementation (BiFC), and biochemical and functional readouts, we show that this interaction occurs in the intestine of animals at the onset of sexual maturity and suffices to support the reproductive program. Our electron micrographs and functional assays provide evidence that intestinal PBX/MEIS cooperation drives another process that depends on lipid mobilization: the formation of an impermeable epicuticle. Without this lipid-rich protective layer, mutant animals are hypersensitive to exogenous oxidative stress and are poor partners for mating. Dedicated communication between the hypodermis and intestine in C. elegans likely supports these physiological outcomes, and we propose a fundamental role for the conserved PBX/MEIS interaction in multicellular signaling networks that rely on lipid homeostasis. Public Library of Science 2019-11-01 /pmc/articles/PMC6824563/ /pubmed/31675356 http://dx.doi.org/10.1371/journal.pbio.3000499 Text en © 2019 Van de Walle et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Van de Walle, Pieter
Geens, Ellen
Baggerman, Geert
José Naranjo-Galindo, Francisco
Askjaer, Peter
Schoofs, Liliane
Temmerman, Liesbet
CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title_full CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title_fullStr CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title_full_unstemmed CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title_short CEH-60/PBX regulates vitellogenesis and cuticle permeability through intestinal interaction with UNC-62/MEIS in Caenorhabditis elegans
title_sort ceh-60/pbx regulates vitellogenesis and cuticle permeability through intestinal interaction with unc-62/meis in caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824563/
https://www.ncbi.nlm.nih.gov/pubmed/31675356
http://dx.doi.org/10.1371/journal.pbio.3000499
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