Literature DB >> 12089524

Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX.

Celia A May1, Angela C Shone, Luba Kalaydjieva, Antti Sajantila, Alec J Jeffreys.   

Abstract

Crossover between the human sex chromosomes during male meiosis is restricted to the terminal pseudoautosomal pairing regions. An obligatory exchange occurs in PAR1, an Xp/Yp pseudoautosomal region of 2.6 Mb, which creates a male-specific recombination 'hot domain' with a recombination rate that is about 20 times higher than the genome average. Low-resolution analysis of PAR1 suggests that crossovers are distributed fairly randomly. By contrast, linkage disequilibrium (LD) and sperm crossover analyses indicate that crossovers in autosomal regions tend to cluster into 'hot spots' of 1-2 kb that lie between islands of disequilibrium of tens to hundreds of kilobases. To determine whether at high resolution this autosomal pattern also applies to PAR1, we have examined linkage disequilibrium over an interval of 43 kb around the gene SHOX. Here we show that in northern European populations, disequilibrium decays rapidly with physical distance, which is consistent with this interval of PAR1 being recombinationally active in male meiosis. Analysis of a subregion of 9.9 kb in sperm shows, however, that crossovers are not distributed randomly, but instead cluster into an intense recombination hot spot that is very similar in morphology to autosomal hot spots. Thus, PAR1 crossover activity may be influenced by male-specific hot spots that are highly suitable for characterization by sperm DNA analysis.

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Year:  2002        PMID: 12089524     DOI: 10.1038/ng918

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  38 in total

1.  Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature.

Authors:  Sara Benito-Sanz; Miriam Aza-Carmona; Amaya Rodríguez-Estevez; Ixaso Rica-Etxebarria; Ricardo Gracia; Angel Campos-Barros; Karen E Heath
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

2.  DNA enrichment by allele-specific hybridization (DEASH): a novel method for haplotyping and for detecting low-frequency base substitutional variants and recombinant DNA molecules.

Authors:  Alec J Jeffreys; Celia A May
Journal:  Genome Res       Date:  2003-10       Impact factor: 9.043

Review 3.  Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved.

Authors:  Norman Arnheim; Peter Calabrese; Magnus Nordborg
Journal:  Am J Hum Genet       Date:  2003-05-22       Impact factor: 11.025

4.  Patterns of linkage disequilibrium in the MHC region on human chromosome 6p.

Authors:  Annette Stenzel; Timothy Lu; W Andreas Koch; Jochen Hampe; Simone M Guenther; Francisco M De La Vega; Michael Krawczak; Stefan Schreiber
Journal:  Hum Genet       Date:  2004-01-22       Impact factor: 4.132

5.  Assessing the performance of the haplotype block model of linkage disequilibrium.

Authors:  Jeffrey D Wall; Jonathan K Pritchard
Journal:  Am J Hum Genet       Date:  2003-08-11       Impact factor: 11.025

6.  Extended linkage disequilibrium surrounding the hemoglobin E variant due to malarial selection.

Authors:  Jun Ohashi; Izumi Naka; Jintana Patarapotikul; Hathairad Hananantachai; Gary Brittenham; Sornchai Looareesuwan; Andrew G Clark; Katsushi Tokunaga
Journal:  Am J Hum Genet       Date:  2004-04-27       Impact factor: 11.025

7.  Insights into recombination from patterns of linkage disequilibrium in humans.

Authors:  Susan E Ptak; Kristian Voelpel; Molly Przeworski
Journal:  Genetics       Date:  2004-05       Impact factor: 4.562

Review 8.  Meiotic recombination hot spots and human DNA diversity.

Authors:  Alec J Jeffreys; J Kim Holloway; Liisa Kauppi; Celia A May; Rita Neumann; M Timothy Slingsby; Adam J Webb
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2004-01-29       Impact factor: 6.237

9.  Preimplantation genetic diagnosis (PGD) for SHOX-related haploinsufficiency in conjunction with trisomy 21 detection by molecular analysis.

Authors:  Gheona Altarescu; Orit Reish; Paul Renbaum; Ester Kasterstein; Dvorah Komarovsky; Alisa Komsky; Orna Bern; Dvorah Strassburger; Ephrat Levy-Lahad; Raphael Ron-El
Journal:  J Assist Reprod Genet       Date:  2010-12-01       Impact factor: 3.412

10.  htSNPer1.0: software for haplotype block partition and htSNPs selection.

Authors:  Keyue Ding; Jing Zhang; Kaixin Zhou; Yan Shen; Xuegong Zhang
Journal:  BMC Bioinformatics       Date:  2005-03-01       Impact factor: 3.169

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