Cargando…

Evolutionary dynamics of the human pseudoautosomal regions

Recombination between the X and Y human sex chromosomes is limited to the two pseudoautosomal regions (PARs) that present quite distinct evolutionary origins. Despite the crucial importance for male meiosis, genetic diversity patterns and evolutionary dynamics of these regions are poorly understood....

Descripción completa

Detalles Bibliográficos
Autores principales: Monteiro, Bruno, Arenas, Miguel, Prata, Maria João, Amorim, António
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084340/
https://www.ncbi.nlm.nih.gov/pubmed/33872316
http://dx.doi.org/10.1371/journal.pgen.1009532
_version_ 1783686134586408960
author Monteiro, Bruno
Arenas, Miguel
Prata, Maria João
Amorim, António
author_facet Monteiro, Bruno
Arenas, Miguel
Prata, Maria João
Amorim, António
author_sort Monteiro, Bruno
collection PubMed
description Recombination between the X and Y human sex chromosomes is limited to the two pseudoautosomal regions (PARs) that present quite distinct evolutionary origins. Despite the crucial importance for male meiosis, genetic diversity patterns and evolutionary dynamics of these regions are poorly understood. In the present study, we analyzed and compared the genetic diversity of the PAR regions using publicly available genomic sequences encompassing both PAR1 and PAR2. Comparisons were performed through allele diversities, linkage disequilibrium status and recombination frequencies within and between X and Y chromosomes. In agreement with previous studies, we confirmed the role of PAR1 as a male-specific recombination hotspot, but also observed similar characteristic patterns of diversity in both regions although male recombination occurs at PAR2 to a much lower extent (at least one recombination event at PAR1 and in ≈1% in normal male meioses at PAR2). Furthermore, we demonstrate that both PARs harbor significantly different allele frequencies between X and Y chromosomes, which could support that recombination is not sufficient to homogenize the pseudoautosomal gene pool or is counterbalanced by other evolutionary forces. Nevertheless, the observed patterns of diversity are not entirely explainable by sexually antagonistic selection. A better understanding of such processes requires new data from intergenerational transmission studies of PARs, which would be decisive on the elucidation of PARs evolution and their role in male-driven heterosomal aneuploidies.
format Online
Article
Text
id pubmed-8084340
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-80843402021-05-06 Evolutionary dynamics of the human pseudoautosomal regions Monteiro, Bruno Arenas, Miguel Prata, Maria João Amorim, António PLoS Genet Research Article Recombination between the X and Y human sex chromosomes is limited to the two pseudoautosomal regions (PARs) that present quite distinct evolutionary origins. Despite the crucial importance for male meiosis, genetic diversity patterns and evolutionary dynamics of these regions are poorly understood. In the present study, we analyzed and compared the genetic diversity of the PAR regions using publicly available genomic sequences encompassing both PAR1 and PAR2. Comparisons were performed through allele diversities, linkage disequilibrium status and recombination frequencies within and between X and Y chromosomes. In agreement with previous studies, we confirmed the role of PAR1 as a male-specific recombination hotspot, but also observed similar characteristic patterns of diversity in both regions although male recombination occurs at PAR2 to a much lower extent (at least one recombination event at PAR1 and in ≈1% in normal male meioses at PAR2). Furthermore, we demonstrate that both PARs harbor significantly different allele frequencies between X and Y chromosomes, which could support that recombination is not sufficient to homogenize the pseudoautosomal gene pool or is counterbalanced by other evolutionary forces. Nevertheless, the observed patterns of diversity are not entirely explainable by sexually antagonistic selection. A better understanding of such processes requires new data from intergenerational transmission studies of PARs, which would be decisive on the elucidation of PARs evolution and their role in male-driven heterosomal aneuploidies. Public Library of Science 2021-04-19 /pmc/articles/PMC8084340/ /pubmed/33872316 http://dx.doi.org/10.1371/journal.pgen.1009532 Text en © 2021 Monteiro et al 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 author and source are credited.
spellingShingle Research Article
Monteiro, Bruno
Arenas, Miguel
Prata, Maria João
Amorim, António
Evolutionary dynamics of the human pseudoautosomal regions
title Evolutionary dynamics of the human pseudoautosomal regions
title_full Evolutionary dynamics of the human pseudoautosomal regions
title_fullStr Evolutionary dynamics of the human pseudoautosomal regions
title_full_unstemmed Evolutionary dynamics of the human pseudoautosomal regions
title_short Evolutionary dynamics of the human pseudoautosomal regions
title_sort evolutionary dynamics of the human pseudoautosomal regions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084340/
https://www.ncbi.nlm.nih.gov/pubmed/33872316
http://dx.doi.org/10.1371/journal.pgen.1009532
work_keys_str_mv AT monteirobruno evolutionarydynamicsofthehumanpseudoautosomalregions
AT arenasmiguel evolutionarydynamicsofthehumanpseudoautosomalregions
AT pratamariajoao evolutionarydynamicsofthehumanpseudoautosomalregions
AT amorimantonio evolutionarydynamicsofthehumanpseudoautosomalregions