Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/12078
Title: A major recombination hotspot in the XqYq pseudoautosomal region gives new insight into processing of human gene conversion events
Authors: Sarbajna, Shriparna
Denniff, Matthew
Jeffreys, Alec J.
Neumann, Rita
Artigas, María Soler
Veselis, Amelia
May, Celia A.
First Published: 1-Jun-2014
Publisher: Oxford University Press
Citation: Human Molecular Genetics, 2012, 21 (9), pp. 2029-2038
Abstract: Recombination plays a fundamental role in meiosis. Non-exchange gene conversion (non-crossover, NCO) may facilitate homologue pairing, while reciprocal crossover (CO) physically connects homologues so they orientate appropriately on the meiotic spindle. In males, X–Y homologous pairing and exchange occurs within the two pseudoautosomal regions (PARs) together comprising <5% of the human sex chromosomes. Successful meiosis depends on an obligatory CO within PAR1, while the nature and role of exchange within PAR2 is unclear. Here, we describe the identification and characterization of a typical ∼1 kb wide recombination hotspot within PAR2. We find that both COs and NCOs are strongly modulated in trans by the presumed chromatin remodelling protein PRDM9, and in cis by a single nucleotide polymorphism (SNP) located at the hotspot centre that appears to influence recombination initiation and which causes biased gene conversion in SNP heterozygotes. This, the largest survey to date of human NCOs reveals for the first time substantial inter-individual variation in the NCO:CO ratio. Although the extent of biased transmission at the central marker in COs is similar across men, it is highly variable among NCO recombinants. This suggests that cis-effects are mediated not only through recombination initiation frequencies varying between haplotypes but also through subsequent processing, with the potential to significantly intensify meiotic drive of hotspot-suppressing alleles. The NCO:CO ratio and extent of transmission distortion among NCOs appear to be inter-related, suggesting the existence of two NCO pathways in humans.
DOI Link: 10.1093/hmg/dds019
ISSN: 0964-6906
eISSN: 1460-2083
Links: http://hdl.handle.net/2381/12078
http://hmg.oxfordjournals.org/content/21/9/2029
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © The Author(s) 2012. Deposited with reference to the publisher’s archiving policy available on the SHERPA/RoMEO website.
Description: This is a pre-copyedited, author-produced PDF of an article accepted for publication in Human Molecular Genetics following peer review. The definitive publisher-authenticated version [Human Molecular Genetics, 2012, 21 (9), pp. 2029-2038] is available online at: http://hmg.oxfordjournals.org/content/21/9/2029.
Appears in Collections:Published Articles, Dept. of Genetics

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