Novel classical MHC class I alleles identified in horses by sequencing clones of reverse transcription-PCR products

被引:18
作者
Chung, C [1 ]
Leib, SR [1 ]
Fraser, DG [1 ]
Ellis, SA [1 ]
McGuire, TC [1 ]
机构
[1] Washington State Univ, Dept Vet Microbiol & Pathol, Pullman, WA 99165 USA
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 2003年 / 30卷 / 06期
关键词
D O I
10.1111/j.1365-2370.2003.00420.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Improved typing of horse classical MHC class I is required to more accurately define these molecules and to extend the number identified further than current serological assays. Defining classical MHC class I alleleic polymorphism is important in evaluating cytotoxic T lymphocyte (CTL) responses in horses. In this study, horse classical MHC class I genes were analyzed based on reverse transcription (RT)-PCR amplification of sequences encoding the polymorphic peptide binding region and the more conserved alpha 3, transmembrane and cytoplasmic regions followed by cloning and sequencing. Primer sets included a horse classical MHC class I-specific reverse primer and a forward primer conserved in all known horse MHC class I genes. Sequencing at least 25 clones containing MHC class I sequences from each of 13 horses identified 25 novel sequences and three others which had been described. Of these, nine alleles were identified from different horses or different RT-PCR and 19 putative alleles were identified in multiple clones from the same RT-PCR. The primer pairs did not amplify putative non-classical MHC class I genes as only classical MHC class I and related pseudogenes were found in 462 clones. This method also identified classical MHC class I alleles shared between horses by descent, and defined differences in alleles between horses varying in equine leukocyte antigen (ELA)-A haplotype as determined by serology. However, horses sharing ELA-A haplotypes defined by serotyping did not always share cDNA sequences, suggesting subhaplotypic variations within serologically defined ELA-A haplotypes. The 13 horses in this study had two to five classical MHC class I sequences, indicating that multiple loci code for these genes. Sequencing clones from RT-PCR with classical MHC class I-specific primers should be useful for selection of haplotype matched and mismatched horses for CTL studies, and provides sequence information needed to develop easier and more discriminating typing procedures.
引用
收藏
页码:387 / 396
页数:10
相关论文
共 36 条
  • [1] The major histocompatibility complex of ruminants
    Amills, M
    Ramiya, V
    Norimine, J
    Lewin, HA
    [J]. REVUE SCIENTIFIQUE ET TECHNIQUE-OFFICE INTERNATIONAL DES EPIZOOTIES, 1998, 17 (01): : 108 - 120
  • [2] ANTCZAK DF, 1991, EQUINE INFECT DIS, V6, P99
  • [3] High resolution HLA class I typing by reference strand mediated conformation analysis (RSCA)
    Argüello, JR
    Little, AM
    Bohan, E
    Goldman, JM
    Marsh, SGE
    Madrigal, JA
    [J]. TISSUE ANTIGENS, 1998, 52 (01): : 57 - 66
  • [4] A novel method for simultaneous high resolution identification of HLA-A, HLA-B, and HLA-Cw alleles
    Arguello, R
    Avakian, H
    Goldman, JM
    Madrigal, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) : 10961 - 10965
  • [5] BAILEY E, 1984, ANIM BLOOD GROUPS BI, V15, P123
  • [6] Bailey E, 2000, GENETICS OF THE HORSE, P123, DOI 10.1079/9780851994291.0123
  • [7] BARBIS DP, 1994, IMMUNOGENETICS, V40, P163, DOI 10.1007/BF00188182
  • [8] BERNOCO D, 1987, ANIM GENET, V18, P103, DOI 10.1111/j.1365-2052.1987.tb00749.x
  • [9] BERNOCO D, 1987, ANIM GENET, V18, P81, DOI 10.1111/j.1365-2052.1987.tb00747.x
  • [10] BULL RW, 1983, ANIM BLOOD GROUPS BI, V14, P119