Bukara M, Vincek V, Figueroa F, Klein J
Immunogenetics. 1985;21(6):569-79. doi: 10.1007/BF00395881.
DNA was isolated from 75 mouse strains carrying classical H-2 haplotypes as well as haplotypes derived from wild mice. The DNA was digested with three restriction endonucleases, Bst EII, Eco RI, and Bam HI, the digests hybridized, using the Southern blotting technique, with probes for the class II genes A alpha, A beta, E alpha, and E beta, and the restriction fragment length polymorphism at these loci determined. The analysis revealed that the most polymorphic of the four loci is A beta, followed by E beta, and, at a different level, by E alpha and A alpha. There is a large difference in the degree of polymorphism between the A beta and E beta genes, on the one hand, and the A alpha and E alpha genes, on the other hand. There is no difference in the degree of polymorphism between the A alpha and E alpha genes. These findings do not substantiate previous postulates of a high A alpha polymorphism and they do not agree with the hypothesis that the class II region is divided into highly polymorphic centromeric and less polymorphic telomeric subregions. Rather, it appears that the differences in the degree of polymorphism of the different segments of the class II region are determined by the class II loci themselves. The polymorphism of the less polymorphic class II genes is, however, still greater than the polymorphism of certain other genes on chromosome 17, notably the alpha 4-globin pseudogene. The distribution of polymorphisms at the A beta and E beta loci suggests that even populations occupying relatively small geographical regions differ in alleles at these loci. Sharing of A beta alleles between unrelated populations is yet to be detected. A certain degree of linkage disequilibrium exists among the A alpha, A beta, and E beta loci; by contrast, the E alpha locus appears to vary largely independently of the other class II loci.
从75个携带经典H-2单倍型以及源自野生小鼠的单倍型的小鼠品系中分离出DNA。用三种限制性内切酶Bst EII、Eco RI和Bam HI对DNA进行消化,消化产物通过Southern印迹技术与II类基因Aα、Aβ、Eα和Eβ的探针杂交,并确定这些位点的限制性片段长度多态性。分析表明,四个位点中多态性最高的是Aβ,其次是Eβ,然后在不同水平上是Eα和Aα。一方面,Aβ和Eβ基因之间的多态性程度与另一方面的Aα和Eα基因之间存在很大差异。Aα和Eα基因之间的多态性程度没有差异。这些发现并未证实先前关于Aα高多态性的假设,也与II类区域分为高度多态的着丝粒和低度多态的端粒亚区域的假设不一致。相反,似乎II类区域不同片段的多态性程度差异是由II类位点本身决定的。然而,低度多态的II类基因的多态性仍然大于17号染色体上某些其他基因的多态性,特别是α4-珠蛋白假基因。Aβ和Eβ位点的多态性分布表明,即使占据相对较小地理区域的群体在这些位点的等位基因上也存在差异。尚未检测到不相关群体之间Aβ等位基因的共享。Aα、Aβ和Eβ位点之间存在一定程度的连锁不平衡;相比之下,Eα位点似乎在很大程度上独立于其他II类位点而变化。