Watts S, Davis A C, Gaut B, Wheeler C, Hill L, Goodenow R S
Department of Genetics, University of California, Berkeley 94720.
EMBO J. 1989 Jun;8(6):1749-59. doi: 10.1002/j.1460-2075.1989.tb03568.x.
We have determined the structure and organization of the entire Qa family of class I genes from the major histocompatibility complex of the C3H mouse. Restriction maps of overlapping lambda and cosmid clones reveal that there are only five Qak genes: Q1k, Q2k, Q4k, Q10k and a Q5/9 hybrid, presumably generated by unequal homologous recombination. The resulting deletion of Q6-Q9 is consistent with the Qa-2null phenotype of this mouse strain. We have sequenced the Qak genes, and predict that each may encode a class I molecule with a structure comparable with that proposed for the transplantation antigens. Furthermore, these Qa products should be able to bind peptides and interact with appropriate T-cell receptors. Interestingly, in comparing Qak and H-2k sequences, we find limited evidence of interlocus gene conversion between Qa and H-2 loci, suggesting that the Qa genes are not likely to serve as a reservoir of genetic information for the generation of H-2 diversity within this haplotype.
我们已经确定了来自C3H小鼠主要组织相容性复合体的整个I类基因Qa家族的结构和组织。重叠的λ噬菌体和黏粒克隆的限制性图谱显示,只有五个Qak基因:Q1k、Q2k、Q4k、Q10k和一个Q5/9杂种,推测是由不等位同源重组产生的。由此导致的Q6-Q9缺失与该小鼠品系的Qa-2无效表型一致。我们已经对Qak基因进行了测序,并预测每个基因可能编码一种I类分子,其结构与移植抗原所提出的结构相当。此外,这些Qa产物应该能够结合肽并与合适的T细胞受体相互作用。有趣的是,在比较Qak和H-2k序列时,我们发现Qa和H-2位点之间基因座间基因转换的证据有限,这表明Qa基因不太可能作为该单倍型内产生H-2多样性的遗传信息库。