Paul E, Livneh A, Manheimer-Lory A J, Diamond B
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461.
J Immunol. 1991 Oct 15;147(8):2771-6.
We report the cDNA sequence of an expressed human V lambda II gene and present an RFLP analysis of the Ig gene family defined by this clone. This V lambda II gene was expressed in a monoclonal B cell line generated from a patient with SLE by transformation with EBV. The encoded lambda L chain displays the 8.12 Id, an Id common to anti-DNA antibodies from patients with SLE. Using a coding region probe we estimate from Southern blot analysis that the germline V lambda II gene family contains at least 15 members. Many of the V lambda II restriction fragments are polymorphic both in SLE patients and in nonautoimmune individuals. EcoRI, HindIII, and TaqI RFLP analyses of the V lambda II gene family and EcoRI analysis of the C lambda gene family reveal no polymorphisms specific to SLE. Observed V lambda II and C lambda allele frequencies are the same among SLE patients and nonautoimmune individuals, and show no evidence of linkage disequilibrium between the two loci.
我们报道了一个表达的人类VλII基因的cDNA序列,并对由该克隆定义的Ig基因家族进行了RFLP分析。这个VλII基因在通过EBV转化从一名SLE患者产生的单克隆B细胞系中表达。编码的λ轻链显示8.12 Id,这是SLE患者抗DNA抗体共有的Id。使用编码区探针,我们通过Southern印迹分析估计种系VλII基因家族至少包含15个成员。许多VλII限制性片段在SLE患者和非自身免疫个体中都是多态性的。VλII基因家族的EcoRI、HindIII和TaqI RFLP分析以及Cλ基因家族的EcoRI分析均未发现SLE特有的多态性。在SLE患者和非自身免疫个体中观察到的VλII和Cλ等位基因频率相同,并且没有显示出两个基因座之间存在连锁不平衡的证据。