Analysis of polymorphisms in the major expressed class I locus (B-FIV) of the chicken

被引:67
作者
Hunt, HD
Fulton, JE
机构
[1] USDA ARS, Avian Dis & Oncol Lab, E Lansing, MI 48823 USA
[2] Hy Line Int, Dallas Ctr, IA 50063 USA
关键词
Mhc; class I; BF; concerted evolution;
D O I
10.1007/s002510050383
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We analyzed the polymorphic nature of eleven alleles expressed by the major class I locus (B-FIV) in chickens. Similar to mammalian class I loci, the nucleotide substitutions with high variability occur in exons 2 and 3 encoding the alpha 1 and alpha 2 domains. However, the nonsynon ymous to synonymous ratio of nucleotide substitutions in exon 3 encoding the alpha helix and beta sheets is reversed compared with HLA. The region of exon 3 encoding the alpha 2 helix demonstrates a much lower nonsynonymous to synonymous ratio, suggesting evolutionary selection of a more conserved alpha 2 helix in B-FIV compared with HLA. Amino acid residues with high Wu-Kabat variability are typically located in positions predicted to impact antigen presentation. B-FIV amino acid residues predicted to interact with the CDR1 alpha region of the T-cell receptor (Tcr) demonstrate less variability than in mouse and human class I alleles. The combination of a reduced nonsynonymous to synonymous ratio in exon 3 encoding the alpha 2 helix and the limited variability in CDR1 alpha contact residues is discussed with regard to concerted evolution between a minimal major histocompatibility complex and compaction of Tcr variable gene segments in the chicken.
引用
收藏
页码:456 / 467
页数:12
相关论文
共 34 条
[1]  
Abplanalp Hans, 1992, Poultry Science Reviews, V4, P29
[2]   The T-cell receptor beta chain-encoding gene repertoire of a New World primate species, the cotton-top tamarin [J].
Allen, TM ;
Lanchbury, JS ;
Hughes, AL ;
Watkins, DI .
IMMUNOGENETICS, 1996, 45 (02) :151-160
[3]  
Arden Bernhard, 1995, Immunogenetics, V42, P455
[4]  
Arden Bernhard, 1995, Immunogenetics, V42, P501
[5]   INFLUENCE OF TURKEY HERPESVIRUS VACCINATION ON THE B-HAPLOTYPE EFFECT ON MAREKS-DISEASE RESISTANCE IN 15.B-CONGENIC CHICKENS [J].
BACON, LD ;
WITTER, RL .
AVIAN DISEASES, 1992, 36 (02) :378-385
[6]   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
[7]   EVOLUTION OF MAJOR HISTOCOMPATIBILITY COMPLEX POLYMORPHISMS AND T-CELL RECEPTOR DIVERSITY IN PRIMATES [J].
BONTROP, RE ;
OTTING, N ;
SLIERENDREGT, BL ;
LANCHBURY, JS .
IMMUNOLOGICAL REVIEWS, 1995, 143 :33-62
[8]   MAREKS-DISEASE - EFFECTS OF B-HISTOCOMPATIBILITY ALLOALLELES IN RESISTANT AND SUSCEPTIBLE CHICKEN LINES [J].
BRILES, WE ;
STONE, HA ;
COLE, RK .
SCIENCE, 1977, 195 (4274) :193-195
[9]   NOMENCLATURE FOR CHICKEN MAJOR HISTOCOMPATIBILITY (B) COMPLEX [J].
BRILES, WE ;
BUMSTEAD, N ;
EWERT, DL ;
GILMOUR, DG ;
GOGUSEV, J ;
HALA, K ;
KOCH, C ;
LONGENECKER, BM ;
NORDSKOG, AW ;
PINK, JRL ;
SCHIERMAN, LW ;
SIMONSEN, M ;
TOIVANEN, A ;
TOIVANEN, P ;
VAINIO, O ;
WICK, G .
IMMUNOGENETICS, 1982, 15 (05) :441-447
[10]   IDENTIFICATION OF HAPLOTYPES OF THE CHICKEN MAJOR HISTOCOMPATIBILITY COMPLEX (B) [J].
BRILES, WE ;
BRILES, RW .
IMMUNOGENETICS, 1982, 15 (05) :449-459