Karr R W, Gregersen P K, Obata F, Goldberg D, Maccari J, Alber C, Silver J
J Immunol. 1986 Nov 1;137(9):2886-90.
A cDNA library was constructed from a DR7, DRw53, DQw2 homozygous cell line, cDNA clones corresponding to DR beta and DQ beta chains were isolated, and the nucleotide sequences of the polymorphic first domains of these chains were determined. A novel screening strategy allowed rapid and simple identification of cDNA clones corresponding to both DR beta chains (DR7 beta1 and DR7 beta2): DR7 beta2 clones have a recognition site for the enzyme BssHII, whereas DR7 beta1 clones do not. The DR7 beta 1 sequence differs significantly from all previously described DR beta chains. As predicted by the presence of the BssHII site in DR7 beta 2 clones, the DR7 beta 2 sequence differs from the DR7 beta 1 sequence. The sequence of the DRw53-associated DR7 beta 2 chain is identical to the reported sequence of the DRw53-associated DR4 beta 2 chain. In addition, the sequence of the DQ beta chain from the DR7, DQw2 cell line is identical to the reported sequence of a DQ beta chain from a DR3, DQw2 cell. These findings raise interesting questions about the evolution of the DR3, DR4, and DR7 haplotypes.
从一个DR7、DRw53、DQw2纯合细胞系构建了一个cDNA文库,分离出与DRβ和DQβ链对应的cDNA克隆,并测定了这些链多态性第一结构域的核苷酸序列。一种新的筛选策略使得能够快速简单地鉴定出与两条DRβ链(DR7β1和DR7β2)对应的cDNA克隆:DR7β2克隆具有BssHII酶的识别位点,而DR7β1克隆没有。DR7β1序列与所有先前描述的DRβ链有显著差异。正如DR7β2克隆中BssHII位点的存在所预测的那样,DR7β2序列与DR7β1序列不同。与DRw53相关的DR7β2链的序列与报道的与DRw53相关的DR4β2链的序列相同。此外,来自DR7、DQw2细胞系的DQβ链的序列与报道的来自DR3、DQw2细胞的DQβ链的序列相同。这些发现引发了关于DR3、DR4和DR7单倍型进化的有趣问题。