Genetic polymorphism of the swine major histocompatibility complex (SLA) class I genes, SLA-1, -2 and -3

被引:50
作者
Ando, A
Kawata, H
Shigenari, A
Anzai, T
Ota, M
Katsuyama, Y
Sada, M
Goto, R
Takeshima, S
Aida, Y
Iwanaga, T
Fujimura, N
Suzuki, Y
Gojobori, T
Inoko, H [1 ]
机构
[1] Tokai Univ, Sch Med, Dept Mol Life Sci, Div Basic Med Sci & Mol Med, Kanagawa 2591193, Japan
[2] Tokai Univ, Sch Med, Teaching & Res Support Ctr, Kanagawa 2591193, Japan
[3] Shinshu Univ, Sch Med, Dept Pharm, Nagano 3908621, Japan
[4] Shinshu Univ, Sch Med, Dept Legal Med, Nagano 3908621, Japan
[5] Natl Cardiovasc Ctr, Dept Reprod Med, Osaka 5658565, Japan
[6] RIKEN, Retrovirus Res Unit, Wako, Saitama 3510198, Japan
[7] Japan Farm Co Ltd, Kagoshima 8952526, Japan
[8] Natl Inst Genet, Ctr Informat Biol, Shizuoka 4118540, Japan
[9] Natl Inst Genet, DNA Data Bank Japan, Shizuoka 4118540, Japan
关键词
SLA; classical class I genes; polymorphism; positive selection; antigen recognition sites;
D O I
10.1007/s00251-003-0619-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In order to identify and characterize genetic polymorphism of the swine major histocompatibility complex (Mhc: SLA) class I genes, RT-PCR products of the second and third exons of the three SLA classical class I genes, SLA-1, SLA-2 and SLA-3 were subjected to nucleotide determination. These analyses allowed the identification of four, eight and seven alleles at the SLA-1, SLA-2 and SLA-3 loci, respectively, from three different breeds of miniature swine and one mixed breed. Among them, 12 alleles were novel. Construction of a phylogenetic tree using the nucleotide sequences of those 19 alleles indicated that the SLA-1 and -2 genes are more closely related to each other than to SLA-3. Selective forces operating at single amino acid sites of the SLA class I molecules were analyzed by the Adaptsite Package program. Ten positive selection sites were found at the putative antigen recognition sites (ARSs). Among the 14 positively selected sites observed in the human MHC (HLA) classical class I molecules, eight corresponding positions in the SLA class I molecules were inferred as positively selected. On the other hand, four amino acids at the putative ARSs were identified as negatively selected in the SLA class I molecules. These results suggest that selective forces operating in the SLA class I molecules are almost similar to those of the HLA class I molecules, although several functional sites for antigen and cytotoxic T-lymphocyte recognition by the SLA class I molecules may be different from those of the HLA class I molecules.
引用
收藏
页码:583 / 593
页数:11
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