The complex mutation pattern of a microsatellite

被引:33
作者
Macaubas, C
Jin, L
Hallmayer, J
Kimura, A
Mignot, E
机构
[1] STANFORD UNIV,DEPT PSYCHIAT,CTR NARCOLEPSY,PALO ALTO,CA 94304
[2] STANFORD UNIV,DEPT GENET,PALO ALTO,CA 94304
[3] TOKYO MED & DENT UNIV,MED RES INST,DEPT TISSUE PHYSIOL,TOKYO 101,JAPAN
来源
GENOME RESEARCH | 1997年 / 7卷 / 06期
关键词
D O I
10.1101/gr.7.6.635
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DQCAR is a [CA](n) microsatellite located in the HLA class ii region and tightly linked to HLA-DQB1. Previous studies showed a strikingly low level of size variation in DQCAR alleles within an extensive subfamily of HLA-DQ subtypes [DQ1]. DQCAR alleles in non-DQ1 subtypes showed a higher degree of size polymorphism. In this study sequence analysis demonstrates that DQ1- associated DQCAR alleles have a single C-->A nucleotide substitution interupting the CA repeat array. Frequent CA-->GA mutations are also observed in DQ1-associated microsatellites with identical allele sizes. In contrast, DQCAR alleles associated with non-DQ1 haplotypes display a perfect CA repeat sequence and the variation in allele size is attributable only to differences in the number of CA repeats. Our results imply that several mutational mechanisms are involved in the generation of allelic diversity within the same microsatellite locus. The possibility of different mutation rates in the same locus should to be taken into account when using these markers in evolutionary and disease studies.
引用
收藏
页码:635 / 641
页数:7
相关论文
共 39 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]  
BLANCK G, 1988, J IMMUNOL, V141, P1734
[3]   HIGH-RESOLUTION OF HUMAN EVOLUTIONARY TREES WITH POLYMORPHIC MICROSATELLITES [J].
BOWCOCK, AM ;
RUIZLINARES, A ;
TOMFOHRDE, J ;
MINCH, E ;
KIDD, JR ;
CAVALLISFORZA, LL .
NATURE, 1994, 368 (6470) :455-457
[4]   EVIDENCE FOR A MECHANISM PREDISPOSING TO INTERGENERATIONAL CAG REPEAT INSTABILITY IN SPINOCEREBELLAR ATAXIA TYPE-I [J].
CHUNG, MY ;
RANUM, LPW ;
DUVICK, LA ;
SERVADIO, A ;
ZOGHBI, HY ;
ORR, HT .
NATURE GENETICS, 1993, 5 (03) :254-258
[5]  
DEKA R, 1995, AM J HUM GENET, V56, P461
[6]   A comprehensive genetic map of the human genome based on 5,264 microsatellites [J].
Dib, C ;
Faure, S ;
Fizames, C ;
Samson, D ;
Drouot, N ;
Vignal, A ;
Millasseau, P ;
Marc, S ;
Hazan, J ;
Seboun, E ;
Lathrop, M ;
Gyapay, G ;
Morissette, J ;
Weissenbach, J .
NATURE, 1996, 380 (6570) :152-154
[7]   MUTATIONAL PROCESSES OF SIMPLE-SEQUENCE REPEAT LOCI IN HUMAN-POPULATIONS [J].
DIRIENZO, A ;
PETERSON, AC ;
GARZA, JC ;
VALDES, AM ;
SLATKIN, M ;
FREIMER, NB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3166-3170
[8]  
EDWARDS A, 1992, P NATL ACAD SCI USA, V91, P3166
[9]   LENGTH OF UNINTERRUPTED CGG REPEATS DETERMINES INSTABILITY IN THE FMR1 GENE [J].
EICHLER, EE ;
HOLDEN, JJA ;
POPOVICH, BW ;
REISS, AL ;
SNOW, K ;
THIBODEAU, SN ;
RICHARDS, CS ;
WARD, PA ;
NELSON, DL .
NATURE GENETICS, 1994, 8 (01) :88-94
[10]  
ESTOUP A, 1995, MOL BIOL EVOL, V12, P1074