Ochi A, Hawley R G, Shulman M J, Hozumi N
Nature. 1983;302(5906):340-2. doi: 10.1038/302340a0.
The expression of immunoglobulin (Ig) genes is regulated at several levels. For example, although kappa-chain production requires a DNA rearrangement that juxtaposes variable and joining segments, this rearrangement is not sufficient for kappa-chain gene expression; that is, some cell types do not permit immunoglobulin production. The mechanisms responsible for the regulation of the expression of rearranged immunoglobulin genes are poorly understood. The technique of modifying cloned genes in vitro and transferring the modified genes to cells in culture provides a tool for identifying the structural features required for gene expression. To analyse immunoglobulin genes in this manner, however, it is first necessary to use, as recipients, cells that normally permit immunoglobulin production. We report here that a cloned kappa-chain gene is expressed in immunoglobulin-producing hybridoma cells. Furthermore, the product of the transferred kappa-chain gene is capable of restoring specific antibody production to the transformed cells.
免疫球蛋白(Ig)基因的表达在多个水平上受到调控。例如,尽管κ链的产生需要DNA重排,使可变区和连接区并列,但这种重排对于κ链基因的表达并不充分;也就是说,某些细胞类型不允许产生免疫球蛋白。负责调控重排免疫球蛋白基因表达的机制目前还知之甚少。体外修饰克隆基因并将修饰后的基因转移到培养细胞中的技术为鉴定基因表达所需的结构特征提供了一种工具。然而,要以这种方式分析免疫球蛋白基因,首先必须使用通常允许产生免疫球蛋白的细胞作为受体。我们在此报告,一个克隆的κ链基因在产生免疫球蛋白的杂交瘤细胞中表达。此外,转移的κ链基因的产物能够使转化细胞恢复特异性抗体的产生。