Lin C R, Chen W S, Kruiger W, Stolarsky L S, Weber W, Evans R M, Verma I M, Gill G N, Rosenfeld M G
Science. 1984 May 25;224(4651):843-8. doi: 10.1126/science.6326261.
In order to further define the mechanisms by which polypeptide growth factors regulate gene transcription and cellular growth, expression cloning techniques were used to select human epidermal growth factor (EGF) receptor complementary DNA clones. The EGF 3' coding domain shows striking homology to the transforming gene product of avian erythroblastosis virus (v-erbB). Over-expression of EGF receptors in A431 cell lines correlates with increased EGF receptor mRNA levels and amplification (up to 110 times) of the apparently singular EGF receptor gene. There appear to be three cytoplasmic polyadenylated RNA products of EGF receptor gene expression in A431 cells, one of which contains only 5' (EGF binding domain) sequences and is postulated to encode the secreted EGF receptor-related protein.
为了进一步确定多肽生长因子调节基因转录和细胞生长的机制,采用表达克隆技术筛选人表皮生长因子(EGF)受体互补DNA克隆。EGF的3'编码结构域与禽成红细胞增多症病毒(v-erbB)的转化基因产物具有显著同源性。A431细胞系中EGF受体的过表达与EGF受体mRNA水平的增加以及明显单一的EGF受体基因的扩增(高达110倍)相关。在A431细胞中,EGF受体基因表达似乎有三种细胞质聚腺苷酸化RNA产物,其中一种仅包含5'(EGF结合结构域)序列,据推测可编码分泌型EGF受体相关蛋白。