Combriato G, Klobeck H G
Institut für Physiologische Chemie, Universität, Munich, FRG.
Eur J Immunol. 1991 Jun;21(6):1513-22. doi: 10.1002/eji.1830210627.
We have cloned a region of 124 kb of the human immunoglobulin lambda light chain locus on chromosome 22 encompassing seven V lambda and seven J-C lambda gene segments. No further C lambda gene segment was found in a region of 35 kb downstream of C lambda 7, which encodes the Ke+Oz- isotype. The C lambda proximal V lambda gene segment V lambda III. 1 is located 14.5 kb upstream of C lambda 1. The five sequenced V lambda genes have the same transcriptional orientation as the J-C lambda gene segments which is likely to be true for the majority of the V lambda gene segments in the human lambda locus and which suggests a deletion mechanism for DNA rearrangement. This is supported by hybridization of V lambda gene probes to germ-line and rearranged DNA from lambda light chain-producing cell lines. Sequences of 23 cDNA clones allow to establish a V lambda subgroup classification based on nucleic acid sequence data and an estimate of the J-C lambda usage.
我们已经克隆了位于22号染色体上的人类免疫球蛋白λ轻链基因座的一个124kb区域,该区域包含7个Vλ和7个J-Cλ基因片段。在编码Ke+Oz-同种型的Cλ7下游35kb区域内未发现其他Cλ基因片段。Cλ近端的Vλ基因片段VλIII.1位于Cλ1上游14.5kb处。5个已测序的Vλ基因与J-Cλ基因片段具有相同的转录方向,这可能适用于人类λ基因座中的大多数Vλ基因片段,这表明DNA重排存在缺失机制。这一点得到了Vλ基因探针与来自λ轻链产生细胞系的种系DNA和重排DNA杂交的支持。23个cDNA克隆的序列能够基于核酸序列数据建立Vλ亚组分类,并估计J-Cλ的使用情况。