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Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function
Respiratory electron transport in mitochondria is coupled to ATP synthesis while generating mutagenic oxygen free radicals. Mitochondrial DNA mutation then accumulates with age, and may set a limit to the lifespan of individual, multicellular organisms. Why is this mutation not inherited? Here we de...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814205/ https://www.ncbi.nlm.nih.gov/pubmed/24068653 http://dx.doi.org/10.1093/gbe/evt147 |
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author | de Paula, Wilson B.M. Agip, Ahmed-Noor A. Missirlis, Fanis Ashworth, Rachel Vizcay-Barrena, Gema Lucas, Cathy H. Allen, John F. |
author_facet | de Paula, Wilson B.M. Agip, Ahmed-Noor A. Missirlis, Fanis Ashworth, Rachel Vizcay-Barrena, Gema Lucas, Cathy H. Allen, John F. |
author_sort | de Paula, Wilson B.M. |
collection | PubMed |
description | Respiratory electron transport in mitochondria is coupled to ATP synthesis while generating mutagenic oxygen free radicals. Mitochondrial DNA mutation then accumulates with age, and may set a limit to the lifespan of individual, multicellular organisms. Why is this mutation not inherited? Here we demonstrate that female gametes—oocytes—have unusually small and simple mitochondria that are suppressed for DNA transcription, electron transport, and free radical production. By contrast, male gametes—sperm—and somatic cells of both sexes transcribe mitochondrial genes for respiratory electron carriers and produce oxygen free radicals. This germ-line division between mitochondria of sperm and egg is observed in both the vinegar fruitfly and the zebrafish—species spanning a major evolutionary divide within the animal kingdom. We interpret these findings as an evidence that oocyte mitochondria serve primarily as genetic templates, giving rise, irreversibly and in each new generation, to the familiar energy-transducing mitochondria of somatic cells and male gametes. Suppressed mitochondrial metabolism in the female germ line may therefore constitute a mechanism for increasing the fidelity of mitochondrial DNA inheritance. |
format | Online Article Text |
id | pubmed-3814205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38142052013-10-31 Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function de Paula, Wilson B.M. Agip, Ahmed-Noor A. Missirlis, Fanis Ashworth, Rachel Vizcay-Barrena, Gema Lucas, Cathy H. Allen, John F. Genome Biol Evol Research Article Respiratory electron transport in mitochondria is coupled to ATP synthesis while generating mutagenic oxygen free radicals. Mitochondrial DNA mutation then accumulates with age, and may set a limit to the lifespan of individual, multicellular organisms. Why is this mutation not inherited? Here we demonstrate that female gametes—oocytes—have unusually small and simple mitochondria that are suppressed for DNA transcription, electron transport, and free radical production. By contrast, male gametes—sperm—and somatic cells of both sexes transcribe mitochondrial genes for respiratory electron carriers and produce oxygen free radicals. This germ-line division between mitochondria of sperm and egg is observed in both the vinegar fruitfly and the zebrafish—species spanning a major evolutionary divide within the animal kingdom. We interpret these findings as an evidence that oocyte mitochondria serve primarily as genetic templates, giving rise, irreversibly and in each new generation, to the familiar energy-transducing mitochondria of somatic cells and male gametes. Suppressed mitochondrial metabolism in the female germ line may therefore constitute a mechanism for increasing the fidelity of mitochondrial DNA inheritance. Oxford University Press 2013 2013-09-25 /pmc/articles/PMC3814205/ /pubmed/24068653 http://dx.doi.org/10.1093/gbe/evt147 Text en © The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article de Paula, Wilson B.M. Agip, Ahmed-Noor A. Missirlis, Fanis Ashworth, Rachel Vizcay-Barrena, Gema Lucas, Cathy H. Allen, John F. Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title | Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title_full | Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title_fullStr | Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title_full_unstemmed | Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title_short | Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function |
title_sort | female and male gamete mitochondria are distinct and complementary in transcription, structure, and genome function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814205/ https://www.ncbi.nlm.nih.gov/pubmed/24068653 http://dx.doi.org/10.1093/gbe/evt147 |
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