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Pronounced somatic bottleneck in mitochondrial DNA of human hair

Heteroplasmy is the presence of variable mitochondrial DNA (mtDNA) within the same individual. The dynamics of heteroplasmy allele frequency among tissues of the human body is not well understood. Here, we measured allele frequency at heteroplasmic sites in two to eight hairs from each of 11 humans...

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Autores principales: Barrett, Alison, Arbeithuber, Barbara, Zaidi, Arslan, Wilton, Peter, Paul, Ian M., Nielsen, Rasmus, Makova, Kateryna D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939377/
https://www.ncbi.nlm.nih.gov/pubmed/31787049
http://dx.doi.org/10.1098/rstb.2019.0175
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author Barrett, Alison
Arbeithuber, Barbara
Zaidi, Arslan
Wilton, Peter
Paul, Ian M.
Nielsen, Rasmus
Makova, Kateryna D.
author_facet Barrett, Alison
Arbeithuber, Barbara
Zaidi, Arslan
Wilton, Peter
Paul, Ian M.
Nielsen, Rasmus
Makova, Kateryna D.
author_sort Barrett, Alison
collection PubMed
description Heteroplasmy is the presence of variable mitochondrial DNA (mtDNA) within the same individual. The dynamics of heteroplasmy allele frequency among tissues of the human body is not well understood. Here, we measured allele frequency at heteroplasmic sites in two to eight hairs from each of 11 humans using next-generation sequencing. We observed a high variance in heteroplasmic allele frequency among separate hairs from the same individual—much higher than that for blood and cheek tissues. Our population genetic modelling estimated the somatic bottleneck during embryonic follicle development of separate hairs to be only 11.06 (95% confidence interval 0.6–34.0) mtDNA segregating units. This bottleneck is much more drastic than somatic bottlenecks for blood and cheek tissues (136 and 458 units, respectively), as well as more drastic than, or comparable to, the germline bottleneck (equal to 25–32 or 7–10 units, depending on the study). We demonstrated that hair undergoes additional genetic drift before and after the divergence of mtDNA lineages of individual hair follicles. Additionally, we showed a positive correlation between donor's age and variance in heteroplasmy allele frequency in hair. These findings have important implications for forensics and for our understanding of mtDNA dynamics in the human body. This article is part of the theme issue ‘Linking the mitochondrial genotype to phenotype: a complex endeavour’.
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spelling pubmed-69393772020-01-03 Pronounced somatic bottleneck in mitochondrial DNA of human hair Barrett, Alison Arbeithuber, Barbara Zaidi, Arslan Wilton, Peter Paul, Ian M. Nielsen, Rasmus Makova, Kateryna D. Philos Trans R Soc Lond B Biol Sci Articles Heteroplasmy is the presence of variable mitochondrial DNA (mtDNA) within the same individual. The dynamics of heteroplasmy allele frequency among tissues of the human body is not well understood. Here, we measured allele frequency at heteroplasmic sites in two to eight hairs from each of 11 humans using next-generation sequencing. We observed a high variance in heteroplasmic allele frequency among separate hairs from the same individual—much higher than that for blood and cheek tissues. Our population genetic modelling estimated the somatic bottleneck during embryonic follicle development of separate hairs to be only 11.06 (95% confidence interval 0.6–34.0) mtDNA segregating units. This bottleneck is much more drastic than somatic bottlenecks for blood and cheek tissues (136 and 458 units, respectively), as well as more drastic than, or comparable to, the germline bottleneck (equal to 25–32 or 7–10 units, depending on the study). We demonstrated that hair undergoes additional genetic drift before and after the divergence of mtDNA lineages of individual hair follicles. Additionally, we showed a positive correlation between donor's age and variance in heteroplasmy allele frequency in hair. These findings have important implications for forensics and for our understanding of mtDNA dynamics in the human body. This article is part of the theme issue ‘Linking the mitochondrial genotype to phenotype: a complex endeavour’. The Royal Society 2020-01-20 2019-12-02 /pmc/articles/PMC6939377/ /pubmed/31787049 http://dx.doi.org/10.1098/rstb.2019.0175 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Barrett, Alison
Arbeithuber, Barbara
Zaidi, Arslan
Wilton, Peter
Paul, Ian M.
Nielsen, Rasmus
Makova, Kateryna D.
Pronounced somatic bottleneck in mitochondrial DNA of human hair
title Pronounced somatic bottleneck in mitochondrial DNA of human hair
title_full Pronounced somatic bottleneck in mitochondrial DNA of human hair
title_fullStr Pronounced somatic bottleneck in mitochondrial DNA of human hair
title_full_unstemmed Pronounced somatic bottleneck in mitochondrial DNA of human hair
title_short Pronounced somatic bottleneck in mitochondrial DNA of human hair
title_sort pronounced somatic bottleneck in mitochondrial dna of human hair
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939377/
https://www.ncbi.nlm.nih.gov/pubmed/31787049
http://dx.doi.org/10.1098/rstb.2019.0175
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