» Articles » PMID: 33872316

Evolutionary Dynamics of the Human Pseudoautosomal Regions

Overview
Journal PLoS Genet
Specialty Genetics
Date 2021 Apr 19
PMID 33872316
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Integration of long-read sequencing, DNA methylation and gene expression reveals heterogeneity in Y chromosome segment lengths in phenotypic males with 46,XX testicular disorder/difference of sex development.

Berglund A, Johannsen E, Skakkebaek A, Chang S, Rohayem J, Laurentino S Biol Sex Differ. 2024; 15(1):77.

PMID: 39380113 PMC: 11463111. DOI: 10.1186/s13293-024-00654-8.


Worse than nothing at all: the inequality of fusions joining autosomes to the PAR and non-PAR portions of sex chromosomes.

Wilhoit K, Alexander E, Blackmon H PeerJ. 2024; 12:e17740.

PMID: 39071118 PMC: 11276758. DOI: 10.7717/peerj.17740.


Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome.

Chen D, Roshandel D, Wang Z, Sun L, Paterson A Hum Mol Genet. 2023; 33(6):543-551.

PMID: 38073250 PMC: 10939428. DOI: 10.1093/hmg/ddad201.


Genomic and demographic processes differentially influence genetic variation across the human X chromosome.

Cotter D, Webster T, Wilson M PLoS One. 2023; 18(11):e0287609.

PMID: 37910456 PMC: 10619814. DOI: 10.1371/journal.pone.0287609.


Analysis of genetic variability in Turner syndrome linked to long-term clinical features.

Suntharalingham J, Ishida M, Cameron-Pimblett A, McGlacken-Byrne S, Buonocore F, Del Valle I Front Endocrinol (Lausanne). 2023; 14:1227164.

PMID: 37800145 PMC: 10548239. DOI: 10.3389/fendo.2023.1227164.


References
1.
Bissegger M, Laurentino T, Roesti M, Berner D . Widespread intersex differentiation across the stickleback genome - The signature of sexually antagonistic selection?. Mol Ecol. 2019; 29(2):262-271. DOI: 10.1111/mec.15255. View

2.
Charlesworth B, Jordan C, Charlesworth D . The evolutionary dynamics of sexually antagonistic mutations in pseudoautosomal regions of sex chromosomes. Evolution. 2014; 68(5):1339-50. PMC: 4289941. DOI: 10.1111/evo.12364. View

3.
Visootsak J, Graham Jr J . Klinefelter syndrome and other sex chromosomal aneuploidies. Orphanet J Rare Dis. 2006; 1:42. PMC: 1634840. DOI: 10.1186/1750-1172-1-42. View

4.
Jeffreys A, Neumann R, Panayi M, Myers S, Donnelly P . Human recombination hot spots hidden in regions of strong marker association. Nat Genet. 2005; 37(6):601-6. DOI: 10.1038/ng1565. View

5.
Flaquer A, Rappold G, Wienker T, Fischer C . The human pseudoautosomal regions: a review for genetic epidemiologists. Eur J Hum Genet. 2008; 16(7):771-9. DOI: 10.1038/ejhg.2008.63. View