Ch'ang L Y, Yen C P, Besl L, Schell M, Solomon A
Department of Medicine, University of Tennessee Medical Center/Graduate School of Medicine, Knoxville 37920.
Mol Immunol. 1994 May;31(7):531-6. doi: 10.1016/0161-5890(94)90040-x.
We have isolated from a human genomic library a potentially functional and distinctive germline gene, designated IGLV6S1, that encodes for light chains of the V lambda VI subgroup. An identical germline gene was cloned from fibroblasts obtained from a patient with light-chain-associated amyloidosis (AL amyloidosis) whose serum and urine contained, respectively, a monoclonal IgG lambda VI protein and a lambda VI Bence Jones protein. Isolation and characterization of cDNA cloned from the patient's bone marrow-derived monoclonal plasma cells revealed that the nucleotide and predicted protein sequences of the rearranged gene were approximately 95% and approximately 90% homologous to those of the germline gene, respectively. The finding that the transcriptional start site for lambda VI RNA synthesis was located upstream of the putative TATA-box promoter, rather than downstream as found for the V lambda II subgroup, implies that a different transcriptional machinery controls the expression of the human V lambda VI-gene family.
我们从人类基因组文库中分离出一个潜在具有功能且独特的种系基因,命名为IGLV6S1,它编码VλVI亚组的轻链。从一名轻链相关淀粉样变性(AL淀粉样变性)患者的成纤维细胞中克隆出了一个相同的种系基因,该患者的血清和尿液中分别含有一种单克隆IgGλVI蛋白和一种λVI本周氏蛋白。从患者骨髓来源的单克隆浆细胞中克隆出的cDNA的分离和鉴定表明,重排基因的核苷酸序列和预测的蛋白质序列分别与种系基因的序列具有约95%和约90%的同源性。λVI RNA合成的转录起始位点位于假定的TATA盒启动子上游,而不是像VλII亚组那样位于下游,这一发现意味着不同的转录机制控制着人类VλVI基因家族的表达。