Literature DB >> 22893033

Meiotic recombinations within major histocompatibility complex of human embryos.

Fulya Taylan1, Ender Altiok.   

Abstract

We studied the rate and pattern of recombinations within the extended major histocompatibility complex (MHC) locus of the human embryos obtained during preimplantation genetic diagnosis (PGD) for HLA compatibility. Recombinant allele frequency was on average 5.33 %, and recombination rate was 0.44 cM/Mb in the 12.2 Mb of the extended MHC locus. Recombination rate varied up to 14-fold (0.19-2.73 cM/Mb) between cases, and maternal recombination rate was on average 3.8 times higher than paternal alleles. More than 69 % of the recombination hot spots were clustered within the extended class II region where the recombination rate was 5.4 times more than that in extended class I region. These findings indicate the potential of PGD to study the mechanisms of linkage disequilibrium within MHC locus of human embryos, demonstrate the recombination characteristics within extended MHC loci of human embryos in comparison to sperm and family studies, and point to the significance of design and interpretation of PGD for HLA compatibility to avoid misdiagnosis because of meiotic recombinations.

Entities:  

Mesh:

Year:  2012        PMID: 22893033     DOI: 10.1007/s00251-012-0644-y

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  40 in total

1.  A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families.

Authors:  A Sanchez-Mazas; S Djoulah; M Busson; I Le Monnier de Gouville; J C Poirier; C Dehay; D Charron; L Excoffier; S Schneider; A Langaney; J Dausset; J Hors
Journal:  Eur J Hum Genet       Date:  2000-01       Impact factor: 4.246

Review 2.  Recombination within the human MHC.

Authors:  M Carrington
Journal:  Immunol Rev       Date:  1999-02       Impact factor: 12.988

Review 3.  MHC class I molecules and KIRs in human history, health and survival.

Authors:  Peter Parham
Journal:  Nat Rev Immunol       Date:  2005-03       Impact factor: 53.106

4.  Sequence variants in the RNF212 gene associate with genome-wide recombination rate.

Authors:  Augustine Kong; Gudmar Thorleifsson; Hreinn Stefansson; Gisli Masson; Agnar Helgason; Daniel F Gudbjartsson; Gudrun M Jonsdottir; Sigurjon A Gudjonsson; Sverrir Sverrisson; Theodora Thorlacius; Aslaug Jonasdottir; Gudmundur A Hardarson; Stefan T Palsson; Michael L Frigge; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Science       Date:  2008-01-31       Impact factor: 47.728

5.  The experience of two European preimplantation genetic diagnosis centres on human leukocyte antigen typing.

Authors:  Hilde Van de Velde; Martine De Rycke; Caroline De Man; Kim De Hauwere; Francesco Fiorentino; Semra Kahraman; Guido Pennings; Willem Verpoest; Paul Devroey; Inge Liebaers
Journal:  Hum Reprod       Date:  2008-12-05       Impact factor: 6.918

6.  Recombination fractions in the HLA system based on the data set 'provinces Françaises': indications of haplotype-specific recombination rates.

Authors:  M Thomsen; M Neugebauer; J Arnaud; N Borot; A Sevin; M Baur; A Cambon-Thomsen
Journal:  Eur J Immunogenet       Date:  1994-02

7.  Individual variation in recombination among human males.

Authors:  J Yu; L Lazzeroni; J Qin; M M Huang; W Navidi; H Erlich; N Arnheim
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

8.  Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Authors:  K W Broman; J C Murray; V C Sheffield; R L White; J L Weber
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

9.  Genetic crossovers are predicted accurately by the computed human recombination map.

Authors:  Pavel P Khil; R Daniel Camerini-Otero
Journal:  PLoS Genet       Date:  2010-01-29       Impact factor: 5.917

10.  The fine-scale structure of recombination rate variation in the human genome.

Authors:  Gilean A T McVean; Simon R Myers; Sarah Hunt; Panos Deloukas; David R Bentley; Peter Donnelly
Journal:  Science       Date:  2004-04-23       Impact factor: 47.728

View more
  3 in total

1.  Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma.

Authors:  Maria I New; Yu K Tong; Tony Yuen; Peiyong Jiang; Christian Pina; K C Allen Chan; Ahmed Khattab; Gary J W Liao; Mabel Yau; Se-Min Kim; Rossa W K Chiu; Li Sun; Mone Zaidi; Y M Dennis Lo
Journal:  J Clin Endocrinol Metab       Date:  2014-02-28       Impact factor: 5.958

2.  Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection.

Authors:  Tobias L Lenz; Victor Spirin; Daniel M Jordan; Shamil R Sunyaev
Journal:  Mol Biol Evol       Date:  2016-06-28       Impact factor: 16.240

3.  Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility.

Authors:  Douglas S Goodin; Pouya Khankhanian; Pierre-Antoine Gourraud; Nicolas Vince
Journal:  PLoS One       Date:  2018-02-13       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.