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PMID: 1353477 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Genomic organization of a polymorphic duplicated region centromeric of HLA-B.

Immunogenetics ·Vol. 36 ·No. 4 ·1992-00-00 ·Pages 208-12

Leelayuwat C, Abraham LJ, Tabarias H, Christiansen FT, Dawkins RL

Abstract

The region between tumor necrosis factor (TNF) and HLA-B in the central major histocompatibility complex (MHC) is polymorphic and associated with several autoimmune diseases. The polymorphisms are haplospecific or haplotypic and retained within the same MHC ancestral haplotype (AH). We have cloned this region from four AHs into lambda bacteriophage and found that a highly polymorphic region in the TNF-HLA-B interval is duplicated. Clones from this region isolated from three MHC AHs show two populations. The regions, designated CL1 and CL2, have different sizes of Bam HI fragments carrying the duplicated sequences. These fragments correspond to those seen after Bam HI restriction fragment length polymorphism (RFLP) analysis of genomic DNA from the same cell lines. Pulsed field gel electrophoresis analysis shows that both CL1 and CL2 are in the central MHC and are about 16 kilobases apart. DNA cloning and RFLP analysis demonstrate that the CL region is highly polymorphic but retained within an MHC AH. Polymorphism and duplication are common characteristics of the genes found in the MHC and therefore the CL sequences have the potential to be interesting in this respect.

Related Genes
MeSH Terms
Autoradiography Centromere Cloning, Molecular Electrophoresis, Gel, Pulsed-Field HLA-B Antigens/genetics Major Histocompatibility Complex Multigene Family Polymorphism, Restriction Fragment Length Tumor Necrosis Factor-alpha/genetics
Chemicals
HLA-B Antigens Tumor Necrosis Factor-alpha
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Leelayuwat C
Department of Clinical Immunology, Royal Perth Hospital, Western Australia.
Abraham L J
Tabarias H
Christiansen F T
Dawkins R L
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Article Info
Journal
Immunogenetics
Abbr.
Immunogenetics
ISSN
0093-7711
Published
1992-00-00
Pages
208-12
Language
English
Region
United States
NLM ID
0420404
Subset
IM
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