Merlino G T, Ishii S, Whang-Peng J, Knutsen T, Xu Y H, Clark A J, Stratton R H, Wilson R K, Ma D P, Roe B A, Hunts John, Shimizu Nobuyoshi, Pastan Ira
Mol Cell Biol. 1985 Jul;5(7):1722-34. doi: 10.1128/mcb.5.7.1722-1734.1985.
A431 cells have an amplification of the epidermal growth factor (EGF) receptor gene, the cellular homolog of the v-erb B oncogene, and overproduce an aberrant 2.9-kilobase RNA that encodes a portion of the EGF receptor. A cDNA (pE15) for the aberrant RNA was cloned, sequenced, and used to analyze genomic DNA blots from A431 and normal cells. These data indicate that the aberrant RNA is created by a gene rearrangement within chromosome 7, resulting in a fusion of the 5' portion of the EGF receptor gene to an unidentified region of genomic DNA. The unidentified sequences are amplified to about the same degree (20- to 30-fold) as the EGF receptor sequences. In situ hybridization to chromosomes from normal cells and A431 cells show that both the EGF receptor gene and the unidentified DNA are localized to the p14-p12 region of chromosome 7. By using cDNA fragments to probe DNA blots from mouse-A431 somatic cell hybrids, the rearranged receptor gene was shown to be associated with translocation chromosome M4.
A431细胞具有表皮生长因子(EGF)受体基因的扩增,该基因是v-erb B癌基因的细胞同源物,并且过量产生一种异常的2.9千碱基RNA,该RNA编码EGF受体的一部分。克隆了该异常RNA的cDNA(pE15),进行了测序,并用于分析来自A431细胞和正常细胞的基因组DNA印迹。这些数据表明,该异常RNA是由7号染色体内的基因重排产生的,导致EGF受体基因的5'部分与基因组DNA的一个未鉴定区域融合。未鉴定的序列与EGF受体序列扩增到大致相同的程度(20至30倍)。对正常细胞和A431细胞的染色体进行原位杂交表明,EGF受体基因和未鉴定的DNA都定位于7号染色体的p14-p12区域。通过使用cDNA片段探测来自小鼠-A431体细胞杂种的DNA印迹,显示重排的受体基因与易位染色体M4相关。