Meiotic recombinations within major histocompatibility complex of human embryos

dc.authoridTaylan, Fulya/0000-0002-2907-0235
dc.authorscopusid58685662800
dc.authorscopusid6601988964
dc.authorwosidTaylan, Fulya/V-7121-2019
dc.contributor.authorTaylan, Fulya
dc.contributor.authorAltiok, Ender
dc.date.accessioned2024-05-25T11:24:19Z
dc.date.available2024-05-25T11:24:19Z
dc.date.issued2012
dc.departmentOkan Universityen_US
dc.department-temp[Taylan, Fulya; Altiok, Ender] Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey; [Taylan, Fulya; Altiok, Ender] Acibadem Genet Diag Ctr, Istanbul, Turkey; [Altiok, Ender] Acibadem Univ, Fac Med, Dept Med Biol, Istanbul, Turkeyen_US
dc.descriptionTaylan, Fulya/0000-0002-2907-0235en_US
dc.description.abstractWe 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.en_US
dc.identifier.citation7
dc.identifier.doi10.1007/s00251-012-0644-y
dc.identifier.endpage844en_US
dc.identifier.issn0093-7711
dc.identifier.issn1432-1211
dc.identifier.issue11en_US
dc.identifier.pmid22893033
dc.identifier.scopus2-s2.0-84867887260
dc.identifier.scopusqualityQ2
dc.identifier.startpage839en_US
dc.identifier.urihttps://doi.org/10.1007/s00251-012-0644-y
dc.identifier.urihttps://hdl.handle.net/20.500.14517/803
dc.identifier.volume64en_US
dc.identifier.wosWOS:000309871800006
dc.identifier.wosqualityQ2
dc.language.isoen
dc.publisherSpringeren_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEmbryoen_US
dc.subjectHLAen_US
dc.subjectLinkage disequilibriumen_US
dc.subjectMHCen_US
dc.subjectPGDen_US
dc.subjectPreimplantation genetic diagnosisen_US
dc.subjectRecombinationen_US
dc.titleMeiotic recombinations within major histocompatibility complex of human embryosen_US
dc.typeArticleen_US
dspace.entity.typePublication

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