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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...

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Autores principales: de Paula, Wilson B.M., Agip, Ahmed-Noor A., Missirlis, Fanis, Ashworth, Rachel, Vizcay-Barrena, Gema, Lucas, Cathy H., Allen, John F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
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.
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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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