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A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging
During aging, environmental stressors and mutations along with reduced DNA repair cause germ cell aneuploidy and genome instability, which limits fertility and embryo development. Benevolent commensal microbiota and dietary plants secrete indoles, which improve healthspan and reproductive success, s...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9956122/ https://www.ncbi.nlm.nih.gov/pubmed/36827370 http://dx.doi.org/10.1126/sciadv.ade8653 |
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author | Sonowal, Robert Swimm, Alyson I. Cingolani, Francesca Parulekar, Noyonika Cleverley, Tesia L. Sahoo, Anusmita Ranawade, Ayush Chaudhuri, Debalina Mocarski, Edward S. Koehler, Heather Nitsche, Karolina Mesiano, Sam Kalman, Daniel |
author_facet | Sonowal, Robert Swimm, Alyson I. Cingolani, Francesca Parulekar, Noyonika Cleverley, Tesia L. Sahoo, Anusmita Ranawade, Ayush Chaudhuri, Debalina Mocarski, Edward S. Koehler, Heather Nitsche, Karolina Mesiano, Sam Kalman, Daniel |
author_sort | Sonowal, Robert |
collection | PubMed |
description | During aging, environmental stressors and mutations along with reduced DNA repair cause germ cell aneuploidy and genome instability, which limits fertility and embryo development. Benevolent commensal microbiota and dietary plants secrete indoles, which improve healthspan and reproductive success, suggesting regulation of germ cell quality. We show that indoles prevent aneuploidy and promote DNA repair and embryo viability, which depends on age and genotoxic stress levels and affects embryo quality across generations. In young animals or with low doses of radiation, indoles promote DNA repair and embryo viability; however, in older animals or with high doses of radiation, indoles promote death of the embryo. These studies reveal a previously unknown quality control mechanism by which indole integrates DNA repair and cell death responses to preclude germ cell aneuploidy and ensure transgenerational genome integrity. Such regulation affects healthy aging, reproductive senescence, cancer, and the evolution of genetic diversity in invertebrates and vertebrates. |
format | Online Article Text |
id | pubmed-9956122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99561222023-02-25 A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging Sonowal, Robert Swimm, Alyson I. Cingolani, Francesca Parulekar, Noyonika Cleverley, Tesia L. Sahoo, Anusmita Ranawade, Ayush Chaudhuri, Debalina Mocarski, Edward S. Koehler, Heather Nitsche, Karolina Mesiano, Sam Kalman, Daniel Sci Adv Biomedicine and Life Sciences During aging, environmental stressors and mutations along with reduced DNA repair cause germ cell aneuploidy and genome instability, which limits fertility and embryo development. Benevolent commensal microbiota and dietary plants secrete indoles, which improve healthspan and reproductive success, suggesting regulation of germ cell quality. We show that indoles prevent aneuploidy and promote DNA repair and embryo viability, which depends on age and genotoxic stress levels and affects embryo quality across generations. In young animals or with low doses of radiation, indoles promote DNA repair and embryo viability; however, in older animals or with high doses of radiation, indoles promote death of the embryo. These studies reveal a previously unknown quality control mechanism by which indole integrates DNA repair and cell death responses to preclude germ cell aneuploidy and ensure transgenerational genome integrity. Such regulation affects healthy aging, reproductive senescence, cancer, and the evolution of genetic diversity in invertebrates and vertebrates. American Association for the Advancement of Science 2023-02-24 /pmc/articles/PMC9956122/ /pubmed/36827370 http://dx.doi.org/10.1126/sciadv.ade8653 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Sonowal, Robert Swimm, Alyson I. Cingolani, Francesca Parulekar, Noyonika Cleverley, Tesia L. Sahoo, Anusmita Ranawade, Ayush Chaudhuri, Debalina Mocarski, Edward S. Koehler, Heather Nitsche, Karolina Mesiano, Sam Kalman, Daniel A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title | A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title_full | A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title_fullStr | A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title_full_unstemmed | A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title_short | A microbiota and dietary metabolite integrates DNA repair and cell death to regulate embryo viability and aneuploidy during aging |
title_sort | microbiota and dietary metabolite integrates dna repair and cell death to regulate embryo viability and aneuploidy during aging |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9956122/ https://www.ncbi.nlm.nih.gov/pubmed/36827370 http://dx.doi.org/10.1126/sciadv.ade8653 |
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