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PMID: 6401863 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

Awdeh ZL, Raum D, Yunis EJ, Alper CA

Abstract

The chromosomal distribution of alleles for HLA-A,-B,-C, and -DR and the serum complement protein alleles of factor B and C2 and C4 was studied in normal Caucasian families. Eight combinations of HLA-B, DR, BF, C2, C4A, and C4B markers were found to occur in haplotypes at frequencies significantly higher than expected. In these combinations, which were defined as extended major histocompatibility complex haplotypes, HLA-A showed limited variation. A possible mechanism for the maintenance of extended haplotypes are human analogs of murine t mutants which are characterized by crossover suppression and male transmission bias. One human 6p haplotype, HLA-B8, DR3, SCO1, GLO 2, was found to be transmitted from males to 83% of their offspring. The same haplotype with GLO 1 had no transmission bias. It is suggested that this GLO 2-marked chromosome is a human analog of a murine t mutant.

MeSH Terms
Alleles Complement System Proteins/genetics Galactose Oxidase/genetics Genes, MHC Class II Genetic Linkage Genotype HLA Antigens/genetics HLA-DR Antigens Humans Mutation
Chemicals
HLA Antigens HLA-DR Antigens Complement System Proteins Galactose Oxidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Awdeh Z L
Raum D
Yunis E J
Alper C A
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25 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-01-00
Pages
259-63
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC393352
Subset
IM
Grants
NIAID NIH HHS · AI 14157 · United States
NIAID NIH HHS · AI 15033 · United States
NIADDK NIH HHS · AM 16392 · United States
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