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High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life

Heteroplasmic mitochondrial DNA (mtDNA) mutations are a major cause of inherited disease and contribute to common late-onset human disorders. The late onset and clinical progression of mtDNA-associated disease is thought to be due to changing heteroplasmy levels, but it is not known how and when thi...

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Autores principales: Glynos, Angelos, Bozhilova, Lyuba V., Frison, Michele, Burr, Stephen, Stewart, James B., Chinnery, Patrick F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599618/
https://www.ncbi.nlm.nih.gov/pubmed/37878704
http://dx.doi.org/10.1126/sciadv.adi4038
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author Glynos, Angelos
Bozhilova, Lyuba V.
Frison, Michele
Burr, Stephen
Stewart, James B.
Chinnery, Patrick F.
author_facet Glynos, Angelos
Bozhilova, Lyuba V.
Frison, Michele
Burr, Stephen
Stewart, James B.
Chinnery, Patrick F.
author_sort Glynos, Angelos
collection PubMed
description Heteroplasmic mitochondrial DNA (mtDNA) mutations are a major cause of inherited disease and contribute to common late-onset human disorders. The late onset and clinical progression of mtDNA-associated disease is thought to be due to changing heteroplasmy levels, but it is not known how and when this occurs. Performing high-throughput single-cell genotyping in two mouse models of human mtDNA disease, we saw unanticipated cell-to-cell differences in mtDNA heteroplasmy levels that emerged prenatally and progressively increased throughout life. Proliferating spleen cells and nondividing brain cells had a similar single-cell heteroplasmy variance, implicating mtDNA or organelle turnover as the major force determining cell heteroplasmy levels. The two different mtDNA mutations segregated at different rates with no evidence of selection, consistent with different rates of random genetic drift in vivo, leading to the accumulation of cells with a very high mutation burden at different rates. This provides an explanation for differences in severity seen in human diseases caused by similar mtDNA mutations.
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spelling pubmed-105996182023-10-26 High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life Glynos, Angelos Bozhilova, Lyuba V. Frison, Michele Burr, Stephen Stewart, James B. Chinnery, Patrick F. Sci Adv Biomedicine and Life Sciences Heteroplasmic mitochondrial DNA (mtDNA) mutations are a major cause of inherited disease and contribute to common late-onset human disorders. The late onset and clinical progression of mtDNA-associated disease is thought to be due to changing heteroplasmy levels, but it is not known how and when this occurs. Performing high-throughput single-cell genotyping in two mouse models of human mtDNA disease, we saw unanticipated cell-to-cell differences in mtDNA heteroplasmy levels that emerged prenatally and progressively increased throughout life. Proliferating spleen cells and nondividing brain cells had a similar single-cell heteroplasmy variance, implicating mtDNA or organelle turnover as the major force determining cell heteroplasmy levels. The two different mtDNA mutations segregated at different rates with no evidence of selection, consistent with different rates of random genetic drift in vivo, leading to the accumulation of cells with a very high mutation burden at different rates. This provides an explanation for differences in severity seen in human diseases caused by similar mtDNA mutations. American Association for the Advancement of Science 2023-10-25 /pmc/articles/PMC10599618/ /pubmed/37878704 http://dx.doi.org/10.1126/sciadv.adi4038 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
Glynos, Angelos
Bozhilova, Lyuba V.
Frison, Michele
Burr, Stephen
Stewart, James B.
Chinnery, Patrick F.
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title_full High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title_fullStr High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title_full_unstemmed High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title_short High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life
title_sort high-throughput single-cell analysis reveals progressive mitochondrial dna mosaicism throughout life
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599618/
https://www.ncbi.nlm.nih.gov/pubmed/37878704
http://dx.doi.org/10.1126/sciadv.adi4038
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