Alonso A, Hozumi N, Murialdo H
J Immunol. 1985 Jul;135(1):614-9.
A functionally defective lambda 3-immunoglobulin chain gene has been cloned from plasmacytoma HOPC-1 (gamma 2b, lambda 1). The lambda 3 gene resulted from the juxtaposition of the germline V lambda 1 sequence with a J lambda 3 C lambda 3 gene segment. DNA sequencing of the rearranged V lambda 1 J lambda 3 exon showed the presence of a single base pair deletion at the site of V-J joining. The alteration in the reading frame caused by this deletion generated a stop codon at the 3' end of J lambda 3, thus rendering this gene nonfunctional for light chain production. In addition, a one-point mutation in the J lambda 3-C lambda 3 intron distinguishes the rearranged gene from the unrearranged counterpart. The implications that this rearrangement has in terms of the mechanism of somatic mutations and of selective proliferation of B cells mediated by antigen stimulation are discussed.
已从浆细胞瘤HOPC-1(γ2b,λ1)中克隆出一个功能缺陷型λ3免疫球蛋白链基因。该λ3基因是由种系Vλ1序列与Jλ3Cλ3基因片段并列而成。对重排的Vλ1Jλ3外显子进行DNA测序显示,在V-J连接位点存在一个单碱基对缺失。此缺失导致的阅读框改变在Jλ3的3'端产生了一个终止密码子,从而使该基因在轻链产生方面无功能。此外,Jλ3-Cλ3内含子中的一个点突变使重排基因与未重排的对应基因有所区别。本文讨论了这种重排在体细胞突变机制以及抗原刺激介导的B细胞选择性增殖方面的意义。