EXTENSIVE POLYMORPHISM OF A (CA)(N) MICROSATELLITE LOCATED IN THE HLA-DQA1/DQB1 CLASS-II REGION

被引:38
作者
MACAUBAS, C
HALLMAYER, J
KALIL, J
KIMURA, A
YASUNAGA, S
GRUMET, FC
MIGNOT, E
机构
[1] CTR NARCOLEPSY RES,DEPT PSYCHIAT,PALO ALTO,CA
[2] STANFORD UNIV,SCH MED,DEPT GENET,PALO ALTO,CA 94304
[3] UNIV SAO PAULO,TRANSPLANTAT IMMUNOL LAB,SAO PAULO,BRAZIL
[4] KYUSHU UNIV,MED INST BIOREGULAT,DEPT GENET,FUKUOKA 812,JAPAN
[5] STANFORD UNIV,CTR BLOOD,PALO ALTO,CA 94304
关键词
D O I
10.1016/0198-8859(94)00101-U
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A highly polymorphic (CA)n microsatellite marker (DQCAR), located between the DQA1 and the DQB1 genes, was characterized in four ethnic groups. Based on length polymorphism, 12 alleles could be defined. The marker is located 1- to 2-kb telomeric to the DQB1 gene and 10 kb centromeric to the DQA1 gene and was shown to be in tight linkage disequilibrium with HLA-DQ. Analysis of the linkage disequilibrium pattern revealed little additional diversity in DQ1-associated haplotypes. Almost all DQ1 subjects examined were DQCAR 103 or DQCAR 107 (13 and 15 CA repeats, respectively). In contrast, significant haplotypic diversity was observed for most DQ2-, DQ3-, and DQ4-associated haplotypes. These haplotypes often had longer allele sizes (DQCAR > 111, more than 17 CA repeats) and more DQCAR alleles per haplotype. These haplotypes also carried DQCAR alleles of different sizes, even though they bore the same DQA1 and DQB1 alleles, and sometimes the same DRB1 allele as well. These results indicate that DQCAR could be a useful marker to better define disease associations with HLA. Our results are also consistent with the hypothesis that CAR alleles with higher numbers of repeats have higher mutation rates and that recombination within the HLA-DR/DQ region is haplotype dependent.
引用
收藏
页码:209 / 220
页数:12
相关论文
共 42 条
[1]   CHARACTERIZATION OF A NOVEL DQB1 (DQB1-ASTERISK-0609) ALLELE BY PCR AMPLIFICATION WITH SEQUENCE-SPECIFIC PRIMERS (PCR-SSP) AND NUCLEOTIDE SEQUENCING [J].
ALDENER, A ;
OLERUP, O .
TISSUE ANTIGENS, 1993, 42 (05) :536-538
[2]   SURVEY OF HUMAN AND RAT MICROSATELLITES [J].
BECKMANN, JS ;
WEBER, JL .
GENOMICS, 1992, 12 (04) :627-631
[3]  
BEGOVICH AB, 1992, J IMMUNOL, V148, P249
[4]  
BLANCK G, 1988, J IMMUNOL, V141, P1734
[5]   SEQUENCE-ANALYSIS OF 3 NOVEL DRW14-DRB1 ALLELES [J].
DONG, RP ;
KIMURA, A ;
SASAZUKI, T .
IMMUNOGENETICS, 1992, 36 (02) :130-133
[6]   SHARED EPITOPES AMONG HLA CLASS-II ALLELES - GENE CONVERSION, COMMON ANCESTRY AND BALANCING SELECTION [J].
ERLICH, HA ;
GYLLENSTEN, UB .
IMMUNOLOGY TODAY, 1991, 12 (11) :411-414
[7]  
Falconer D. S., 1989, Introduction to quantitative genetics.
[8]   2 NOVEL HLA-DQB1-ASTERISK-06 ALLELES REVEAL ADDITIONAL HETEROGENEITY OF HLA-DQWL [J].
FENSKE, TS ;
BAXTERLOWE, LA .
TISSUE ANTIGENS, 1992, 40 (01) :49-52
[9]   ALLELES AT 4 HLA CLASS-II LOCI DETERMINED BY OLIGONUCLEOTIDE HYBRIDIZATION AND THEIR ASSOCIATIONS IN 5 ETHNIC-GROUPS [J].
FERNANDEZVINA, MA ;
GAO, XJ ;
MORAES, ME ;
MORAES, JR ;
SALATIEL, I ;
MILLER, S ;
TSAI, J ;
SUN, YP ;
AN, JB ;
LAYRISSE, Z ;
GAZIT, E ;
BRAUTBAR, C ;
STASTNY, P .
IMMUNOGENETICS, 1991, 34 (05) :299-312
[10]  
GERNANDEZVINA MA, 1994, HUM IMMUNOL, V39, P290