Zouali M, Madaio M P, Canoso R T, Stollar B D
Department of Biochemistry, Tufts University Medical School, Boston, MA.
Eur J Immunol. 1989 Sep;19(9):1757-60. doi: 10.1002/eji.1830190934.
To evaluate the degree of genetic polymorphism of the V kappa repertoire in systemic lupus erythematosus (SLE), we performed Southern blot hybridizations with human gene probes corresponding to the four human V kappa gene families. In a comparative analysis, non-lymphoid cell DNA samples from three patients with idiopathic SLE, eight subjects with susceptibility to drug-induced lupus and seven control individuals were digested with the restriction endonucleases Bam HI, Bg 1 II, Eco RI and Hind III, and hybridized sequentially to the four V kappa family-specific probes. The restriction patterns on Southern blots revealed a low degree of polymorphism of the human V kappa gene repertoires of SLE patients and control individuals. This analysis, together with previous parallel studies of the V kappa locus in lupus-prone mice, implies that autoantibody hyperproduction in lupus is not associated with major modifications in the structure or genomic organization of immunoglobulin light chain genes.
为评估系统性红斑狼疮(SLE)中Vκ基因库的遗传多态性程度,我们使用对应于四个人类Vκ基因家族的人类基因探针进行了Southern印迹杂交。在一项比较分析中,来自三名特发性SLE患者、八名对药物性狼疮易感的受试者和七名对照个体的非淋巴细胞DNA样本用限制性内切酶Bam HI、Bg 1 II、Eco RI和Hind III进行消化,并依次与四种Vκ家族特异性探针杂交。Southern印迹上的限制性图谱显示SLE患者和对照个体的人类Vκ基因库多态性程度较低。该分析与先前对狼疮易感小鼠Vκ基因座的平行研究一起表明,狼疮中自身抗体的过度产生与免疫球蛋白轻链基因的结构或基因组组织的重大改变无关。