Literature DB >> 9244441

Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex.

L Malfroy1, M P Roth, M Carrington, N Borot, A Volz, A Ziegler, H Coppin.   

Abstract

Analysis of 784 informative meioses in the CEPH pedigrees revealed a total of 22 recombination events having occurred in the 6-Mb region between D6S265 (70 kb centromeric of HLA-A) and D6S276. These 22 breakpoints were localized with respect to anonymous polymorphic markers, leading to a detailed genetic map of the region telomeric to the human major histocompatibility complex. A nonrandom pattern of recombination was observed throughout this region: the low recombination rate of 0.19% within the 4-Mb interval centromeric to the HLA class I-like candidate gene for hemochromatosis indeed contrasts with the approximate 1% rate observed within the most telomeric two megabases. This reduced rate of recombination may be due to selective constraints depending on environmental factors related to immunity and iron status or to structural variations hampering proper meiotic pairing of homologous sequences. Population data from other human genome segments are now needed to determine whether linkage disequilibrium extending over 4 Mb is unique to this region.

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Year:  1997        PMID: 9244441     DOI: 10.1006/geno.1997.4800

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  20 in total

1.  Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

Authors:  X Liu; D F Barker
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

2.  Evidence for linkage and association with reading disability on 6p21.3-22.

Authors:  D E Kaplan; J Gayán; J Ahn; T-W Won; D Pauls; R K Olson; J C DeFries; F Wood; B F Pennington; G P Page; S D Smith; J R Gruen
Journal:  Am J Hum Genet       Date:  2002-04-10       Impact factor: 11.025

3.  Sequence variation and haplotype structure at the human HFE locus.

Authors:  Christopher Toomajian; Martin Kreitman
Journal:  Genetics       Date:  2002-08       Impact factor: 4.562

4.  A method for detecting recent selection in the human genome from allele age estimates.

Authors:  Christopher Toomajian; Richard S Ajioka; Lynn B Jorde; James P Kushner; Martin Kreitman
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

5.  Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

Authors:  Karen E Deffenbacher; Judith B Kenyon; Denise M Hoover; Richard K Olson; Bruce F Pennington; John C DeFries; Shelley D Smith
Journal:  Hum Genet       Date:  2004-05-11       Impact factor: 4.132

6.  The origin and spread of the HFE-C282Y haemochromatosis mutation.

Authors:  S Distante; K J H Robson; J Graham-Campbell; A Arnaiz-Villena; P Brissot; Mark Worwood
Journal:  Hum Genet       Date:  2004-09       Impact factor: 4.132

7.  Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis.

Authors:  Justin P Rubio; Melanie Bahlo; Niall Tubridy; Jim Stankovich; Rachel Burfoot; Helmut Butzkueven; Caron Chapman; Laura Johnson; Mark Marriott; Grant Mraz; Brian Tait; Chris Wilkinson; Bruce Taylor; Terence P Speed; Simon J Foote; Trevor J Kilpatrick
Journal:  Hum Genet       Date:  2004-03-11       Impact factor: 4.132

Review 8.  Genomic architecture of MHC-linked odorant receptor gene repertoires among 16 vertebrate species.

Authors:  Pablo Sandro Carvalho Santos; Thomas Kellermann; Barbara Uchanska-Ziegler; Andreas Ziegler
Journal:  Immunogenetics       Date:  2010-08-03       Impact factor: 2.846

9.  Allelic association under map error and recombinational heterogeneity: a tale of two sites.

Authors:  C Lonjou; A Collins; R S Ajioka; L B Jorde; J P Kushner; N E Morton
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-15       Impact factor: 11.205

10.  Quantitative-trait locus for specific language and reading deficits on chromosome 6p.

Authors:  J Gayán; S D Smith; S S Cherny; L R Cardon; D W Fulker; A M Brower; R K Olson; B F Pennington; J C DeFries
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

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