Eilers M, Picard D, Yamamoto K R, Bishop J M
Department of Microbiology and Immunology, George Williams Hooper Foundation.
Nature. 1989 Jul 6;340(6228):66-8. doi: 10.1038/340066a0.
The human proto-oncogene myc encodes a nuclear phosphoprotein whose primary biochemical function is still unknown. To facilitate further study of that function, we have created conditional alleles of myc by fusing the hormone-binding domain of the human oestrogen receptor gene to the 5' or the 3' end of human myc. The two chimaeric genes, designated mycer and ermyc, encode proteins that bind oestrogen with high affinity. Expression of one of the genes, mycer, transforms a rat fibroblast cell line in a tightly oestrogen-dependent manner. Transformation is dependent on the presence of a functional myc gene in the chimaera and is reversible upon removal of the hormone. The chimaeric genes will be useful tools to study the mechanisms by which Myc affects cellular phenotype. Recently, chimaeras between the adenovirus E1A protein and the hormone binding domain of the rat glucocorticoid receptor were shown to activate transcription in a manner characteristic for E1A, but in a hormone regulated manner. We therefore asked whether the same strategy could be applied to the product of myc.
人类原癌基因myc编码一种核磷蛋白,其主要生化功能尚不清楚。为便于进一步研究该功能,我们通过将人类雌激素受体基因的激素结合结构域融合到人类myc的5'端或3'端,创建了myc的条件等位基因。这两个嵌合基因,分别命名为mycer和ermyc,编码与雌激素具有高亲和力的蛋白质。其中一个基因mycer的表达以严格的雌激素依赖方式转化大鼠成纤维细胞系。转化依赖于嵌合体中功能性myc基因的存在,并且在去除激素后是可逆的。这些嵌合基因将成为研究Myc影响细胞表型机制的有用工具。最近,有人发现腺病毒E1A蛋白与大鼠糖皮质激素受体的激素结合结构域之间的嵌合体以E1A特有的方式激活转录,但以激素调节的方式进行。因此,我们询问同样的策略是否可以应用于myc的产物。