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PMID: 2563360 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Definition of IDDM-associated HLA DQ and DX RFLPs by segregation analysis of multiplex sibships.

Human immunology ·Vol. 24 ·No. 1 ·1989-01-00 ·Pages 51-63

Carrier CM, Mollen N, Rothman WC, Rodriguez de Cordoba S, Rey-Campos J, Ginsberg-Fellner F, Carpenter C, Rubinstein P

Abstract

Genetic variation of the DQ alpha and beta and of the DX alpha genes, detectable as RFLP in genomic DNA digests, has been suggested to improve the identification of individuals at high risk for insulin-dependent diabetes mellitus (IDDM). DNA from all members of 32 IDDM multiplex families was digested with six restriction endonucleases and the resulting fragments analyzed in Southern blots for hybridization with labeled cDNA probes for those genes. A computerized segregation analysis procedure was then used to assign fragments to haplotypes. Associations among fragments and between fragments and haplotypes characterized serologically and biochemically for their class II genes and IDDM-carrier status were calculated. The results indicate that the alleles of the DX alpha polymorphism maintain linkage disequilibrium with those of the DQ beta genes responsible for the well-known DQ beta 3.2-IDDM association, so that IDDM-carrier haplotypes carry disproportionally often both DQ beta 3.2 and DX alpha-TaqI-2.2kb. Thus, these RFLPs identify a DR-DQ-DX haplotype in high linkage disequilibrium, rather than the locus or loci that account for their high relative risk. However, four DR4-DQ beta 3.2 haplotypes that lack DX alpha-TaqI-2.2kb were encountered, two of which are "affected." These haplotypes suggest that the identification of the "disease locus" can be facilitated by the study of unusual haplotypes in which distinct IDDM-associated alleles occur separated from their neighbors of the standard genetic configurations.

MeSH Terms
Alleles DNA Probes, HLA Diabetes Mellitus, Type 1/genetics,immunology Genes, MHC Class II Genetic Linkage HLA-D Antigens/genetics HLA-DQ Antigens/genetics Haplotypes Humans Polymorphism, Genetic Polymorphism, Restriction Fragment Length
Chemicals
DNA Probes, HLA HLA-D Antigens HLA-DQ Antigens HLA-Dx antigen
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Carrier C M
Department of Immunogenetics, Lindsley F. Kimball Research Institute of the New York Blood Center, NY 10021.
Mollen N
Rothman W C
Rodriguez de Cordoba S
Rey-Campos J
Ginsberg-Fellner F
Carpenter C
Rubinstein P
Article Info
Journal
Human immunology
Abbr.
Hum Immunol
ISSN
0198-8859
Published
1989-01-00
Pages
51-63
Language
English
Region
United States
NLM ID
8010936
Subset
IM
Grants
NIDDK NIH HHS · DK 19631-11 · United States
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