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Genetics and geography of leukocyte telomere length in sub-Saharan Africans
Leukocyte telomere length (LTL) might be causal in cardiovascular disease and major cancers. To elucidate the roles of genetics and geography in LTL variability across humans, we compared LTL measured in 1295 sub-Saharan Africans (SSAs) with 559 African–Americans (AAms) and 2464 European–Americans (...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645709/ https://www.ncbi.nlm.nih.gov/pubmed/32821950 http://dx.doi.org/10.1093/hmg/ddaa187 |
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author | Hunt, Steven C Hansen, Matthew E B Verhulst, Simon McQuillan, Michael A Beggs, William Lai, Tsung-Po Mokone, Gaonyadiwe G Mpoloka, Sununguko Wata Meskel, Dawit Wolde Belay, Gurja Nyambo, Thomas B Abnet, Christian C Yeager, Meredith Chanock, Stephen J Province, Michael A Williams, Scott M Aviv, Abraham Tishkoff, Sarah A |
author_facet | Hunt, Steven C Hansen, Matthew E B Verhulst, Simon McQuillan, Michael A Beggs, William Lai, Tsung-Po Mokone, Gaonyadiwe G Mpoloka, Sununguko Wata Meskel, Dawit Wolde Belay, Gurja Nyambo, Thomas B Abnet, Christian C Yeager, Meredith Chanock, Stephen J Province, Michael A Williams, Scott M Aviv, Abraham Tishkoff, Sarah A |
author_sort | Hunt, Steven C |
collection | PubMed |
description | Leukocyte telomere length (LTL) might be causal in cardiovascular disease and major cancers. To elucidate the roles of genetics and geography in LTL variability across humans, we compared LTL measured in 1295 sub-Saharan Africans (SSAs) with 559 African–Americans (AAms) and 2464 European–Americans (EAms). LTL differed significantly across SSAs (P = 0.003), with the San from Botswana (with the oldest genomic ancestry) having the longest LTL and populations from Ethiopia having the shortest LTL. SSAs had significantly longer LTL than AAms [P = 6.5(e-16)] whose LTL was significantly longer than EAms [P = 2.5(e-7)]. Genetic variation in SSAs explained 52% of LTL variance versus 27% in AAms and 34% in EAms. Adjustment for genetic variation removed the LTL differences among SSAs. LTL genetic variation among SSAs, with the longest LTL in the San, supports the hypothesis that longer LTL was ancestral in humans. Identifying factors driving LTL variation in Africa may have important ramifications for LTL-associated diseases. |
format | Online Article Text |
id | pubmed-7645709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76457092020-11-12 Genetics and geography of leukocyte telomere length in sub-Saharan Africans Hunt, Steven C Hansen, Matthew E B Verhulst, Simon McQuillan, Michael A Beggs, William Lai, Tsung-Po Mokone, Gaonyadiwe G Mpoloka, Sununguko Wata Meskel, Dawit Wolde Belay, Gurja Nyambo, Thomas B Abnet, Christian C Yeager, Meredith Chanock, Stephen J Province, Michael A Williams, Scott M Aviv, Abraham Tishkoff, Sarah A Hum Mol Genet General Article Leukocyte telomere length (LTL) might be causal in cardiovascular disease and major cancers. To elucidate the roles of genetics and geography in LTL variability across humans, we compared LTL measured in 1295 sub-Saharan Africans (SSAs) with 559 African–Americans (AAms) and 2464 European–Americans (EAms). LTL differed significantly across SSAs (P = 0.003), with the San from Botswana (with the oldest genomic ancestry) having the longest LTL and populations from Ethiopia having the shortest LTL. SSAs had significantly longer LTL than AAms [P = 6.5(e-16)] whose LTL was significantly longer than EAms [P = 2.5(e-7)]. Genetic variation in SSAs explained 52% of LTL variance versus 27% in AAms and 34% in EAms. Adjustment for genetic variation removed the LTL differences among SSAs. LTL genetic variation among SSAs, with the longest LTL in the San, supports the hypothesis that longer LTL was ancestral in humans. Identifying factors driving LTL variation in Africa may have important ramifications for LTL-associated diseases. Oxford University Press 2020-08-21 /pmc/articles/PMC7645709/ /pubmed/32821950 http://dx.doi.org/10.1093/hmg/ddaa187 Text en © The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), 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 | General Article Hunt, Steven C Hansen, Matthew E B Verhulst, Simon McQuillan, Michael A Beggs, William Lai, Tsung-Po Mokone, Gaonyadiwe G Mpoloka, Sununguko Wata Meskel, Dawit Wolde Belay, Gurja Nyambo, Thomas B Abnet, Christian C Yeager, Meredith Chanock, Stephen J Province, Michael A Williams, Scott M Aviv, Abraham Tishkoff, Sarah A Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title | Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title_full | Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title_fullStr | Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title_full_unstemmed | Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title_short | Genetics and geography of leukocyte telomere length in sub-Saharan Africans |
title_sort | genetics and geography of leukocyte telomere length in sub-saharan africans |
topic | General Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645709/ https://www.ncbi.nlm.nih.gov/pubmed/32821950 http://dx.doi.org/10.1093/hmg/ddaa187 |
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