Noma Y, Yaoita Y, Matsunami N, Rosén A, Klein G, Honjo T
Mol Biol Med. 1984 Oct;2(5):337-50.
We have studied the immunoglobulin gene organization of ultraviolet light (u.v.)-induced variant cells derived from an Epstein-Barr virus-transformed cell line. One variant produced IgG1 and two variants produced both IgM and IgG1 whereas the parental cell line produced IgM. Southern blot analyses of DNAs of these cells revealed a newly rearranged JH fragment in all the variants. The newly rearranged JH fragment also hybridized with the C gamma 1 sequence. The mu and gamma 1 chains produced in the double isotype-producing variants share the same VH sequence. u.v. illumination also induced rearrangement of the C lambda gene in the IgG1-producing variant. The double isotype producers contained the immunoglobulin gene organization and mutation best explained by fusion of the IgG1 producer and the parental IgM producer.
我们研究了源自爱泼斯坦 - 巴尔病毒转化细胞系的紫外线(u.v.)诱导变异细胞的免疫球蛋白基因组织。一个变异细胞产生IgG1,两个变异细胞同时产生IgM和IgG1,而亲本细胞系产生IgM。对这些细胞的DNA进行的Southern印迹分析显示,所有变异细胞中均有一个新重排的JH片段。这个新重排的JH片段也与Cγ1序列杂交。在产生两种同种型的变异细胞中产生的μ链和γ1链共享相同的VH序列。紫外线照射还诱导了产生IgG1的变异细胞中Cλ基因的重排。产生两种同种型的细胞所含的免疫球蛋白基因组织和突变情况,用产生IgG1的变异细胞与亲本IgM产生细胞的融合来解释最为合适。