Lillehoj E P, Myers N B, Lee D R, Hansen T H, Coligan J E
J Immunol. 1985 Aug;135(2):1271-5.
Comparative tryptic peptide analyses were performed on 12 different D region molecules representing seven different haplotypes. The Dd, Dq, and Dw16 regions were shown to encode multiple, antigenically distinct molecules (Dd Ld, Dq Lq Rq, and Dw16 Lw16, respectively). In addition, each of these molecules was found to have a unique primary structure, implying that they are the products of separate genes. However the previously described Rd molecule, which was identified by sequential immuno-precipitation and 2-D gel analyses, was indistinguishable from Ld by tryptic peptide mapping, implying that these two molecules may be products of the same gene. The Db, Ddx, Dk, and Dp regions were found to determine a single molecule with the reagents tested. Intra- and/or inter-haplotype comparisons of the peptide maps of each of these D region molecules revealed widely disparate structural relationships. For example, the Db, Dq, Lq, Rq, Dw16, and Lw16 molecules all showed striking homology with the Ld molecule. Members of this family share between 43 to 55% peptide homology with Ld, indicating a high conservation of primary structure (greater than 90%). However, because Dq and Dw16 region-encoded molecules show no exceptional relationship to each other, the portion of the conserved sequence is not the same for each of these Ld-like molecules. By contrast, comparisons of the Dk, Dd, Ddx, and Dp molecules with Ld or with each other revealed tryptic peptide homologies ranging from 22 to 38%, suggesting a sequence homology of 70 to 85%. When compared with the Kb molecule, each of the D region molecules showed between 21 to 36% peptide map homology (70 to 85% sequence homology). These studies indicate, therefore, that there is a family of Ld-like molecules representing several distinct haplotypes. This definition of a highly homologous family of D region molecules suggests that many D-region molecules have evolved from an Ld-like primordial gene and that in different haplotypes different portions of this prototypic structure have been maintained.
对代表七种不同单倍型的12种不同的D区分子进行了胰蛋白酶肽分析。结果表明,Dd、Dq和Dw16区域编码多种抗原性不同的分子(分别为Dd、Ld、Dq、Lq、Rq和Dw16、Lw16)。此外,发现这些分子中的每一个都具有独特的一级结构,这意味着它们是不同基因的产物。然而,通过连续免疫沉淀和二维凝胶分析鉴定的先前描述的Rd分子,通过胰蛋白酶肽图谱分析与Ld无法区分,这意味着这两种分子可能是同一基因的产物。发现Db、Ddx、Dk和Dp区域用所测试的试剂确定单一分子。对这些D区分子中每一个的肽图谱进行单倍型内和/或单倍型间比较,揭示了广泛不同的结构关系。例如,Db、Dq、Lq、Rq、Dw16和Lw16分子都与Ld分子显示出显著的同源性。该家族成员与Ld的肽同源性在43%至55%之间,表明一级结构高度保守(大于90%)。然而,由于Dq和Dw16区域编码的分子彼此之间没有特殊关系,这些类Ld分子中每一个的保守序列部分并不相同。相比之下,将Dk、Dd、Ddx和Dp分子与Ld或它们彼此进行比较,发现胰蛋白酶肽同源性在22%至38%之间,表明序列同源性为70%至85%。当与Kb分子比较时,每个D区分子的肽图谱同源性在21%至36%之间(序列同源性为70%至85%)。因此,这些研究表明,存在一个代表几种不同单倍型的类Ld分子家族。对D区分子高度同源家族的这一定义表明,许多D区分子是从一个类Ld的原始基因进化而来的,并且在不同的单倍型中,该原型结构的不同部分得以保留。