Gustafsson K, Germana S, Hirsch F, Pratt K, LeGuern C, Sachs D H
Transplantation Biology Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1990 Dec;87(24):9798-802. doi: 10.1073/pnas.87.24.9798.
As part of our studies of the class II genes of miniature swine, we have isolated and characterized cDNA clones corresponding to DRB genes from two major histocompatibility complex homozygous strains. Comparison of the sequences of these clones to those of human DRB genes revealed a striking amino acid homology between the hypervariable residues of SLA-DRBc and the human DRB1-0101 allele. The percentage of differences in these residues between the pig DRBc allele and the human DRB1-0101 allele was significantly lower (29%) than that between the DRB1-0101 allele and all other human alleles (average, 66.2%). This similarity was not seen in a comparison of the number of silent substitutions, by which the swine DRBc and the human DRB-0101 differed. Since phenotypic selection operates at the level of protein products rather than nucleotide sequences, these data suggest the existence of selective mechanisms that have resulted in similar hypervariable regions in certain alleles even in these widely disparate species. Consistent with this hypothesis, an examination of available murine and bovine class II sequences revealed a homology in hypervariable residues between the human DRB1-1401 allele and the mouse E beta s allele as well as a cow DRB allele. Consideration of these data along with intraspecies allelic sequence comparisons suggests that at least some of the interspecies similarities have emerged as the result of convergent evolution, possibly as the result of a need to react to common pathogens.
作为我们对小型猪Ⅱ类基因研究的一部分,我们从两个主要组织相容性复合体纯合品系中分离并鉴定了与DRB基因相对应的cDNA克隆。将这些克隆的序列与人类DRB基因的序列进行比较,发现SLA - DRBc的高变残基与人类DRB1 - 0101等位基因之间存在显著的氨基酸同源性。猪DRBc等位基因与人类DRB1 - 0101等位基因在这些残基上的差异百分比(29%)明显低于DRB1 - 0101等位基因与所有其他人等位基因之间的差异百分比(平均为66.2%)。在比较猪DRBc和人类DRB - 0101的沉默替代数量时,未发现这种相似性。由于表型选择作用于蛋白质产物而非核苷酸序列水平,这些数据表明存在选择性机制,导致即使在这些差异很大的物种中,某些等位基因也具有相似的高变区。与这一假设一致,对现有的小鼠和牛Ⅱ类序列进行检查发现,人类DRB1 - 1401等位基因与小鼠Eβs等位基因以及牛DRB等位基因在高变残基上存在同源性。综合这些数据以及种内等位基因序列比较结果表明,至少部分种间相似性是趋同进化的结果,可能是由于需要对常见病原体作出反应。