Patterns of variation of the major histocompatibility complex class IIB loci in Chinese goose (Anser Cygnoides)

被引:2
作者
Zhou, Xu [1 ,2 ]
Li, Chunjin [1 ,2 ]
Yi, Kangle [1 ,2 ]
Liang, Hongyan [1 ,2 ]
Chen, Lu [1 ,2 ]
Sun, Yanling [1 ,2 ]
Niu, Shuling [1 ,2 ]
Wu, Wei [3 ]
机构
[1] Jilin Univ, Coll Anim Sci & Vet Med, Changchun 130062, Jilin Province, Peoples R China
[2] Jilin Univ, Jilin Prov Key Lab Anim Embryo Engn, Changchun 130062, Jilin Province, Peoples R China
[3] Jilin Agr Univ, Coll Anim Sci & Technol, Changchun 130118, Peoples R China
关键词
Goose; MHC class II; Polymorphism; Evolution; MHC CLASS-II; MINIMAL-ESSENTIAL-MHC; PASSERINE BIRD; GENES; POLYMORPHISM; SELECTION; HAPLOTYPES; EVOLUTION; QUAIL; CDNA;
D O I
10.1007/s00251-009-0374-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In order to understand the variations of genomic organization of the major histocompatibility complex (MHC) and provide data for the studies on disease resistance of avian species, the MHC class II polymorphism in Chinese Z-goose was investigated for the first time in the present study. Eight alleles, which probably came from different loci, were found in six different geese with only one obvious band in the restriction fragment length polymorphism data. The numbers of nonsynonymous substitutions (dN) in peptide binding region of exon 2 were higher than that of synonymous substitutions (dS), and no stop codons or frameshift mutations were found in this region, indicating that balance selection was in operation, and the sequences are not likely to be pseudogenes. In addition, we successfully obtained five different long MHC class II fragments (about 1,162 bp) in six geese and found that the length of intron 1 was longer than that in chicken and some other birds, but intron 2 seemed to be intermediate in length. The phylogenetic tree appeared to branch in an order consistent with accepted evolutionary pathway.
引用
收藏
页码:443 / 450
页数:8
相关论文
共 46 条
[21]   The chicken B locus is a minimal essential major histocompatibility complex [J].
Kaufman, J ;
Milne, S ;
Göbel, TWF ;
Walker, BA ;
Jacob, JP ;
Auffray, C ;
Zoorob, R ;
Beck, S .
NATURE, 1999, 401 (6756) :923-925
[22]   A MINIMAL-ESSENTIAL-MHC AND AN UNRECOGNIZED-MHC - 2 EXTREMES IN SELECTION FOR POLYMORPHISM [J].
KAUFMAN, J ;
VOLK, H ;
WALLNY, HJ .
IMMUNOLOGICAL REVIEWS, 1995, 143 :63-88
[23]  
KLEIN J, 1990, IMMUNOGENETICS, V31, P217, DOI 10.1007/BF00204890
[24]  
Klein J., 1986, NATURAL HIST MAJOR H
[25]   MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment [J].
Kumar, S ;
Tamura, K ;
Nei, M .
BRIEFINGS IN BIOINFORMATICS, 2004, 5 (02) :150-163
[26]   The dominant MHC class I gene is adjacent to the polymorphic TAP2 gene in the duck, Anas platyrhynchos [J].
Mesa, CM ;
Thulien, KJ ;
Moon, DA ;
Veniamin, SM ;
Magor, KE .
IMMUNOGENETICS, 2004, 56 (03) :192-203
[27]   Genetic drift outweighs balancing selection in shaping post-bottleneck major histocompatibility complex variation in New Zealand robins (Petroicidae) [J].
Miller, HC ;
Lambert, DM .
MOLECULAR ECOLOGY, 2004, 13 (12) :3709-3721
[28]   The MHC of the duck (Anas platyrhynchos) contains five differentially expressed class I genes [J].
Moon, DA ;
Veniamin, SM ;
Parks-Dely, JA ;
Magor, KE .
JOURNAL OF IMMUNOLOGY, 2005, 175 (10) :6702-6712
[29]  
NEI M, 1986, MOL BIOL EVOL, V3, P418
[30]   EVOLUTION OF MHC GENETIC DIVERSITY - A TALE OF INCEST, PESTILENCE AND SEXUAL PREFERENCE [J].
POTTS, WK ;
WAKELAND, EK .
TRENDS IN GENETICS, 1993, 9 (12) :408-412