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Population size influences the type of nucleotide variations in humans

BACKGROUND: It is well known that the effective size of a population (N(e)) is one of the major determinants of the amount of genetic variation within the population. However, it is unclear whether the types of genetic variations are also dictated by the effective population size. To examine this, w...

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Autor principal: Subramanian, Sankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894472/
https://www.ncbi.nlm.nih.gov/pubmed/31805852
http://dx.doi.org/10.1186/s12863-019-0798-9
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author Subramanian, Sankar
author_facet Subramanian, Sankar
author_sort Subramanian, Sankar
collection PubMed
description BACKGROUND: It is well known that the effective size of a population (N(e)) is one of the major determinants of the amount of genetic variation within the population. However, it is unclear whether the types of genetic variations are also dictated by the effective population size. To examine this, we obtained whole genome data from over 100 populations of the world and investigated the patterns of mutational changes. RESULTS: Our results revealed that for low frequency variants, the ratio of AT→GC to GC→AT variants (β) was similar across populations, suggesting the similarity of the pattern of mutation in various populations. However, for high frequency variants, β showed a positive correlation with the effective population size of the populations. This suggests a much higher proportion of high frequency AT→GC variants in large populations (e.g. Africans) compared to those with small population sizes (e.g. Asians). These results imply that the substitution patterns vary significantly between populations. These findings could be explained by the effect of GC-biased gene conversion (gBGC), which favors the fixation of G/C over A/T variants in populations. In large population, gBGC causes high β. However, in small populations, genetic drift reduces the effect of gBGC resulting in reduced β. This was further confirmed by a positive relationship between N(e) and β for homozygous variants. CONCLUSIONS: Our results highlight the huge variation in the types of homozygous and high frequency polymorphisms between world populations. We observed the same pattern for deleterious variants, implying that the homozygous polymorphisms associated with recessive genetic diseases will be more enriched with G or C in populations with large N(e) (e.g. Africans) than in populations with small N(e) (e.g. Europeans).
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spelling pubmed-68944722019-12-11 Population size influences the type of nucleotide variations in humans Subramanian, Sankar BMC Genet Research Article BACKGROUND: It is well known that the effective size of a population (N(e)) is one of the major determinants of the amount of genetic variation within the population. However, it is unclear whether the types of genetic variations are also dictated by the effective population size. To examine this, we obtained whole genome data from over 100 populations of the world and investigated the patterns of mutational changes. RESULTS: Our results revealed that for low frequency variants, the ratio of AT→GC to GC→AT variants (β) was similar across populations, suggesting the similarity of the pattern of mutation in various populations. However, for high frequency variants, β showed a positive correlation with the effective population size of the populations. This suggests a much higher proportion of high frequency AT→GC variants in large populations (e.g. Africans) compared to those with small population sizes (e.g. Asians). These results imply that the substitution patterns vary significantly between populations. These findings could be explained by the effect of GC-biased gene conversion (gBGC), which favors the fixation of G/C over A/T variants in populations. In large population, gBGC causes high β. However, in small populations, genetic drift reduces the effect of gBGC resulting in reduced β. This was further confirmed by a positive relationship between N(e) and β for homozygous variants. CONCLUSIONS: Our results highlight the huge variation in the types of homozygous and high frequency polymorphisms between world populations. We observed the same pattern for deleterious variants, implying that the homozygous polymorphisms associated with recessive genetic diseases will be more enriched with G or C in populations with large N(e) (e.g. Africans) than in populations with small N(e) (e.g. Europeans). BioMed Central 2019-12-05 /pmc/articles/PMC6894472/ /pubmed/31805852 http://dx.doi.org/10.1186/s12863-019-0798-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Subramanian, Sankar
Population size influences the type of nucleotide variations in humans
title Population size influences the type of nucleotide variations in humans
title_full Population size influences the type of nucleotide variations in humans
title_fullStr Population size influences the type of nucleotide variations in humans
title_full_unstemmed Population size influences the type of nucleotide variations in humans
title_short Population size influences the type of nucleotide variations in humans
title_sort population size influences the type of nucleotide variations in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894472/
https://www.ncbi.nlm.nih.gov/pubmed/31805852
http://dx.doi.org/10.1186/s12863-019-0798-9
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