Chimini G, Angelini G, Piccioli P, Parodi B, De Totero D, Ferrara G B
Istituto Nazionale per la Ricerca sul Cancro, Viale Benedetto XV, Genova, Italy.
Hum Immunol. 1990 Apr;27(4):348-59. doi: 10.1016/0198-8859(90)90085-4.
A panel of homozygous cell lines, previously typed by primed lymphocyte test for their DPw specificity, have been studied by restriction fragment length polymorphism analysis, using a DP beta-specific probe. Highly stringent hybridization and washing conditions were used to prevent cross-hybridization with DR- and DQ-specific fragments. Three out of six enzymes employed allowed us to distinguish clustered or single DPw specificities, and by MspI digestion it was possible to detect different patterns within a single specificity such as DPw4. Some of the cell lines have been further studied with synthetic oligonucleotides derived from the polymorphic regions of the second exon of DP beta 1 gene, and, in general, a correlation with the primed lymphocyte test--defined specificities and restriction fragment length polymorphism was found. These data suggest a more extended complexity of the DP region, in addition to that defined as the DPw1-DPw6 segregant series.
一组先前通过启动淋巴细胞试验确定其DPw特异性的纯合细胞系,已使用DPβ特异性探针通过限制性片段长度多态性分析进行了研究。采用了高度严格的杂交和洗涤条件,以防止与DR和DQ特异性片段发生交叉杂交。所使用的六种酶中有三种使我们能够区分聚集的或单一的DPw特异性,并且通过MspI消化能够在单一特异性如DPw4内检测到不同的模式。一些细胞系已进一步用源自DPβ1基因第二外显子多态性区域的合成寡核苷酸进行了研究,并且总体上发现与启动淋巴细胞试验定义的特异性和限制性片段长度多态性存在相关性。这些数据表明,除了定义为DPw1 - DPw6分离系列之外,DP区域的复杂性更加广泛。