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Unique sequences for two HLA-DRB1 genes expressed on distinct DRw6 haplotypes
Authors:Effie W. Petersdorf  Robert L. Griffith  Henry A. Erlich  Eric M. Mickelson  Anajane G. Smith  Brenda B. Nisperos  Paul J. Martin  John A. Hansen
Affiliation:(1) Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA;(2) Human Genetics Department, Cetus Corporation, Emeryville, California, USA;(3) Department of Medicine, University of Washington, Seattle, Washington, USA;(4) Division of Clinical Research, Fred Hutchinson Cancer Research Center, 1124 Columbia Street, 98104 Seattle, WA, USA
Abstract:We have used restriction fragment length polymorphism (RFLP) analysis and DNA sequencing to characterize two distinct DRB1 alleles expressed on DRw52 and DQw7-associated haplotypes but not readily defined by conventional DR serology. These two haplotypes, designated HLA-D ldquoHAGrdquo and ldquoPEVrdquo, react variably with DRw13(w6), DRw14(w6), and the more broad DR ldquo3+6rdquo antisera. Analysis of RFLP revealed that HLA-D ldquoHAGrdquo and ldquoPEVrdquo are associated with different DRw52 variants, and that ldquoHAGrdquo is indistinguishable from DRw18(3) haplotypes. Sequencing of the ldquoHAGrdquo and ldquoPEVrdquo DRB1 genes showed each to represent novel alleles. Nevertheless, these sequences show similarities with the other alleles of the DR5, w6, and w8 family. ldquoHAGrdquo (DRB1*1303) appears to have arisen either from two recombinational events involving at least three DRB1 sequences (DRB1*1101, DRB1*0803, DRB1*0401) or from a single recombinational event together with multiple point mutational events. ldquoPEVrdquo appears to represent a DRB1*1301-1302/DRB1*1101 recombinant allele, with recombination having occured in the region of bases 175 – 198. The results of this study suggest that the DRw52 family haplotypes is derived from a relatively restricted number of ancestral sequences, with diversity among DRB1 alleles within this family arising through gene conversion or recombination events.
Keywords:
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