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Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause

Environmental stress can induce adult reproductive diapause, a state of developmental arrest that temporarily suspends reproduction. Deficiency for C. elegans Piwi protein PRG-1 results in strains that reproduce for many generations but then become sterile. We found that sterile-generation prg-1/Piw...

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Autores principales: Heestand, Bree, Simon, Matt, Frenk, Stephen, Titov, Denis, Ahmed, Shawn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918633/
https://www.ncbi.nlm.nih.gov/pubmed/29617657
http://dx.doi.org/10.1016/j.celrep.2018.03.015
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author Heestand, Bree
Simon, Matt
Frenk, Stephen
Titov, Denis
Ahmed, Shawn
author_facet Heestand, Bree
Simon, Matt
Frenk, Stephen
Titov, Denis
Ahmed, Shawn
author_sort Heestand, Bree
collection PubMed
description Environmental stress can induce adult reproductive diapause, a state of developmental arrest that temporarily suspends reproduction. Deficiency for C. elegans Piwi protein PRG-1 results in strains that reproduce for many generations but then become sterile. We found that sterile-generation prg-1/Piwi mutants typically displayed pronounced germ cell atrophy as L4 larvae matured into 1-day-old adults. Atrophied germlines spontaneously reproliferated across the first days of adulthood, and this was accompanied by fertility for day 2–4 adults. Sterile day 5 prg-1 mutant adults remained sterile indefinitely, but providing an alternative food source could restore their fertility. Our data imply that late-generation prg-1 mutants experience a dynamic form of adult reproductive diapause, promoted by stress response, cell death, and RNAi pathways, where delayed fertility and reproductive quiescence represent parallel adaptive developmental outcomes. This may occur in response to a form of “heritable stress” that is transmitted by gametes and epigenetic in nature.
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spelling pubmed-59186332018-04-27 Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause Heestand, Bree Simon, Matt Frenk, Stephen Titov, Denis Ahmed, Shawn Cell Rep Article Environmental stress can induce adult reproductive diapause, a state of developmental arrest that temporarily suspends reproduction. Deficiency for C. elegans Piwi protein PRG-1 results in strains that reproduce for many generations but then become sterile. We found that sterile-generation prg-1/Piwi mutants typically displayed pronounced germ cell atrophy as L4 larvae matured into 1-day-old adults. Atrophied germlines spontaneously reproliferated across the first days of adulthood, and this was accompanied by fertility for day 2–4 adults. Sterile day 5 prg-1 mutant adults remained sterile indefinitely, but providing an alternative food source could restore their fertility. Our data imply that late-generation prg-1 mutants experience a dynamic form of adult reproductive diapause, promoted by stress response, cell death, and RNAi pathways, where delayed fertility and reproductive quiescence represent parallel adaptive developmental outcomes. This may occur in response to a form of “heritable stress” that is transmitted by gametes and epigenetic in nature. 2018-04-03 /pmc/articles/PMC5918633/ /pubmed/29617657 http://dx.doi.org/10.1016/j.celrep.2018.03.015 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Heestand, Bree
Simon, Matt
Frenk, Stephen
Titov, Denis
Ahmed, Shawn
Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title_full Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title_fullStr Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title_full_unstemmed Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title_short Transgenerational Sterility of Piwi Mutants Represents a Dynamic Form of Adult Reproductive Diapause
title_sort transgenerational sterility of piwi mutants represents a dynamic form of adult reproductive diapause
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918633/
https://www.ncbi.nlm.nih.gov/pubmed/29617657
http://dx.doi.org/10.1016/j.celrep.2018.03.015
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