DNA RECOMBINATION AND NATURAL-SELECTION PRESSURE SUSTAIN GENETIC SEQUENCE DIVERSITY OF THE FELINE MHC CLASS-I GENES

被引:36
作者
YUHKI, N
OBRIEN, SJ
机构
[1] Laboratory of Viral Carcinogenesis, National Cancer Institute, Frederick, MD
关键词
D O I
10.1084/jem.172.2.621
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sequence comparisons of seven distinct MHC class I cDNA clones revealed that feline class I molecules have a remarkable similarity to human HLA genes in their organization of functional domains as well as in the nonrandom partitioning of genetic variability according to the functional constraints ascribed to different regions of the MHC molecule. The distribution of the pattern of sequence polymorphism in the cat as compared with genetic diversity of human and mouse class I genes provides evidence for four coordinate factors that contribute to the origin and sustenance of abundant allele diversity that characterizes the MHC in the species. These include: (a) a gradual accumulation of spontaneous mutational substitution over evolutionary time; (b) selection against mutational divergence in regions of the class I molecule involved in T cell receptor interaction and also in certain regions that interact with common features of antigens ; (c) positive selection pressure in favor of persistence of polymorphism and heterozygosity at 57 nucleotide residues that comprise the antigen recognition site; and (d) periodic intragenic (interallelic) and intergenic recombination within the class I genes. We describe a highly conserved 23-bp nucleotide sequence within the coding region of the first α-helix that separates two relatively polymorphic segments located in the α1 domain that may act as a template or "hot spot" for homologous recombination between class I alleles. © 1990, Rockefeller University Press., All rights reserved.
引用
收藏
页码:621 / 630
页数:10
相关论文
共 39 条
[1]   STRUCTURE OF THE HUMAN CLASS-I HISTOCOMPATIBILITY ANTIGEN, HLA-A2 [J].
BJORKMAN, PJ ;
SAPER, MA ;
SAMRAOUI, B ;
BENNETT, WS ;
STROMINGER, JL ;
WILEY, DC .
NATURE, 1987, 329 (6139) :506-512
[2]   THE FOREIGN ANTIGEN-BINDING SITE AND T-CELL RECOGNITION REGIONS OF CLASS-I HISTOCOMPATIBILITY ANTIGENS [J].
BJORKMAN, PJ ;
SAPER, MA ;
SAMRAOUI, B ;
BENNETT, WS ;
STROMINGER, JL ;
WILEY, DC .
NATURE, 1987, 329 (6139) :512-518
[3]   EVOLUTIONARY SIGNIFICANCE OF HL-A SYSTEM [J].
BODMER, WF .
NATURE, 1972, 237 (5351) :139-+
[4]   DIRECT BINDING OF INFLUENZA PEPTIDES TO CLASS-I HLA MOLECULES [J].
CHEN, BP ;
PARHAM, P .
NATURE, 1989, 337 (6209) :743-745
[5]  
COTTER SM, 1975, J AM VET MED ASSOC, V166, P449
[6]  
Davis L. G., 1986, BASIC METHODS MOL BI
[7]   T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION [J].
DAVIS, MM ;
BJORKMAN, PJ .
NATURE, 1988, 334 (6181) :395-402
[8]   ENHANCED IMMUNOLOGICAL SURVEILLANCE IN MICE HETEROZYGOUS AT H-2 GENE COMPLEX [J].
DOHERTY, PC ;
ZINKERNAGEL, RM .
NATURE, 1975, 256 (5512) :50-52
[9]   MHC POLYMORPHISM PREDATING SPECIATION [J].
FIGUEROA, F ;
GUNTHER, E ;
KLEIN, J .
NATURE, 1988, 335 (6187) :265-267
[10]   A SIMPLE AND VERY EFFICIENT METHOD FOR GENERATING CDNA LIBRARIES [J].
GUBLER, U ;
HOFFMAN, BJ .
GENE, 1983, 25 (2-3) :263-269