Demaine A G, Taube D H, Vaughan R W, Kerr L A, Welsh K I
Clin Exp Immunol. 1986 Nov;66(2):406-13.
We describe here, to our knowledge for the first time, associations between polymorphisms at the genomic DNA level in the immunoglobulin gene region and renal diseases which lead to chronic renal failure. Recent studies have shown that protein polymorphisms, present in immunoglobulin (Ig) heavy chains (Gm allotypes) are associated with certain forms of renal disease and with end stage renal failure per se. To investigate this association at the DNA level we have used probes which recognize Ig heavy chain genes and this report describes results obtained with one of these, the S mu switch region probe. With the restriction endonuclease Sst 1 (or the isoschizomer; Sac I) a number of restriction fragment length polymorphisms (RFLP) can be obtained which are recognized by this probe and there is a highly significant association between certain of these and renal disease. This is the first report of Ig switch region polymorphisms being associated with disease, yet our results suggest that S mu RFLP are more closely linked to renal disease than Ig protein polymorphisms.
据我们所知,我们在此首次描述免疫球蛋白基因区域基因组DNA水平的多态性与导致慢性肾衰竭的肾脏疾病之间的关联。最近的研究表明,免疫球蛋白(Ig)重链中存在的蛋白质多态性(Gm同种异型)与某些形式的肾脏疾病以及终末期肾衰竭本身相关。为了在DNA水平上研究这种关联,我们使用了识别Ig重链基因的探针,本报告描述了其中一种探针,即Sμ转换区探针所获得的结果。使用限制性内切酶Sst 1(或同裂酶Sac I),可以获得许多被该探针识别的限制性片段长度多态性(RFLP),其中某些与肾脏疾病之间存在高度显著的关联。这是关于Ig转换区多态性与疾病相关的首次报告,但我们的结果表明,Sμ RFLP与肾脏疾病的联系比Ig蛋白质多态性更为紧密。