The MHC type 1 diabetes susceptibility gene is centromeric to HLA-DQB1

被引:10
作者
Husain, Zaheed [1 ,2 ]
Kelly, M. Ann [7 ]
Eisenbarth, George S. [6 ]
Pugliese, Alberto [5 ]
Awdeh, Zuheir L. [1 ]
Larsen, Charles E. [1 ,3 ]
Alper, Chester A. [1 ,4 ]
机构
[1] Immune Dis Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[5] Univ Miami, Sch Med, Diabet Res Inst, Miami, FL 33101 USA
[6] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Aurora, CO 80045 USA
[7] Univ Birmingham, Sch Med, Div Med Sci, Birmingham B15 2TT, W Midlands, England
关键词
major histocompatibility complex; single nucleotide polymorphism; susceptibility gene; type; 1; diabetes;
D O I
10.1016/j.jaut.2007.10.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HLA-DQB1 is widely considered to be the major histocompatibility complex (MHC) susceptibility gene for type I diabetes (T1D). However, since inheritance of the gene in T1D is recessive, the presence of the protective HLA-DQB1*0602 allele with normal nucleotide sequence in some patients raises the question of whether HLA-DQB1 is not the susceptibility locus itself but merely a good marker. HLA-DQB1*0602 is part of a conserved extended haplotype (CEH) [HLA-B7, SC31, DR2] (137, DR2) with fixed DNA over more than 1 Mb of genomic DNA that normally carries a protective allele at the true susceptibility locus. We postulated that, in patients with HLA-DQB1*0602, the protective allele at the susceptibility locus has been replaced by a susceptibility allele through an ancient crossover at meiosis centromeric to HLA-DQB1. We analyzed single nucleotide polymorphisms (SNPs) distinguishing the HLA-DQA2 (the first expressed gene centromeric to HLA-DQB1) allele on the normal HLA-B7, DR2 CEH from those on susceptibility CEHs in T1D patients and controls with HLA-DQB1*0602. All but 1 of 20 healthy control HLA-DQB1*0602 haplotypes had identical (consensus) first intron HLA-DQA2 5-SNP haplotypes. Fifteen of 19 patients with HLA-DQB1*0602 were homozygous for I or more HLA-DQA2 SNPs differing from consensus HLA-DQA2 SNPs, providing evidence of crossover involving the HLA-DQA2 locus. The remaining 4 patients were heterozygous at all positions and therefore uninformative. The loss of dominant protection usually associated with HLA-DQB1*0602 haplotypes is consistent with a locus centromeric to HLA-DQB1 being a major determinant of MHC-associated susceptibility, and perhaps the true T1D susceptibility locus. (C) 2007 Published by Elsevier Ltd.
引用
收藏
页码:266 / 272
页数:7
相关论文
共 36 条
[1]   A simple estimate of the general population frequency of the MHC susceptibility gene for autoimmune polygenic disease [J].
Alper, CA ;
Dubey, DP ;
Yunis, EJ ;
Awdeh, Z .
EXPERIMENTAL AND CLINICAL IMMUNOGENETICS, 2000, 17 (03) :138-147
[2]   Incomplete penetrance of susceptibility genes for MHC-determined immunoglobulin deficiencies in monozygotic twins discordant for type I diabetes [J].
Alper, Chester A. ;
Husain, Zaheed ;
Larsen, Charles E. ;
Dubey, Devendra P. ;
Stein, Rosanne ;
Day, Caitlin ;
Baker, Alissa ;
Beyan, Huriya ;
Hawa, Mohammed ;
Ola, Thomas O. ;
Leslie, R. David .
JOURNAL OF AUTOIMMUNITY, 2006, 27 (02) :89-95
[3]   The haplotype structure of the human major histocompatibility complex [J].
Alper, Chester A. ;
Larsen, Charles E. ;
Dubey, Devendra P. ;
Awdeh, Zuheir L. ;
Fici, Dolores A. ;
Yunis, Edmond J. .
HUMAN IMMUNOLOGY, 2006, 67 (1-2) :73-84
[4]   Multi-SNP analysis of MHC region - Remarkable conservation of HLA-A1-M-DR3 haplotype [J].
Aly, TA ;
Erer, E ;
Ide, A ;
Gowan, K ;
Babu, SR ;
Erlich, HA ;
Rewers, MJ ;
Eisenbarth, GS ;
Fain, PR .
DIABETES, 2006, 55 (05) :1265-1269
[5]   MAPPING AND NUCLEOTIDE-SEQUENCE OF A NEW HLA CLASS-II LIGHT CHAIN GENE, DQB3 [J].
ANDO, A ;
KAWAI, J ;
MAEDA, M ;
TSUJI, K ;
TROWSDALE, J ;
INOKO, H .
IMMUNOGENETICS, 1989, 30 (04) :243-249
[6]   ISOTYPIC AND ALLOTYPIC VARIATION OF HUMAN CLASS-II HISTOCOMPATIBILITY ANTIGEN ALPHA-CHAIN GENES [J].
AUFFRAY, C ;
LILLIE, JW ;
ARNOT, D ;
GROSSBERGER, D ;
KAPPES, D ;
STROMINGER, JL .
NATURE, 1984, 308 (5957) :327-333
[7]   STRUCTURE AND EXPRESSION OF HLA-DQ-ALPHA AND -DX-ALPHA GENES - INTERALLELIC ALTERNATE SPLICING OF THE HLA-DQ-ALPHA GENE AND FUNCTIONAL SPLICING OF THE HLA-DX-ALPHA GENE USING A RETROVIRAL VECTOR [J].
AUFFRAY, C ;
LILLIE, JW ;
KORMAN, AJ ;
BOSS, JM ;
FRECHIN, N ;
GUILLEMOT, F ;
COOPER, J ;
MULLIGAN, RC ;
STROMINGER, JL .
IMMUNOGENETICS, 1987, 26 (1-2) :63-73
[8]   A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease [J].
Awdeh, Z. L. ;
Yunis, Edmond J. ;
Audeh, Mark J. ;
Fici, Dolores ;
Pugliese, Alberto ;
Larsen, Charles E. ;
Alper, Chester A. .
JOURNAL OF AUTOIMMUNITY, 2006, 27 (03) :174-181
[9]   EXTENDED HLA/COMPLEMENT ALLELE HAPLOTYPES - EVIDENCE FOR T/T-LIKE COMPLEX IN MAN [J].
AWDEH, ZL ;
RAUM, D ;
YUNIS, EJ ;
ALPER, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (01) :259-263
[10]   RESTRICTION FRAGMENT LENGTH POLYMORPHISM ANALYSIS OF HLA HAPLOTYPES IN FAMILIES WITH TYPE-I DIABETES-MELLITUS [J].
BADENHOOP, K ;
SCHWARZ, G ;
BINGLEY, P ;
LEWIS, V ;
DRUMMOND, V ;
GALE, EAM ;
BOTTAZZO, GF .
TISSUE ANTIGENS, 1990, 35 (01) :32-39