Chen C, Nussenzweig A, Guo M, Kim D, Li G C, Ling C C
Department of Medical Physics, Memorial Sloan-Kettering Cancer Center, New York 10021, USA.
Oncogene. 1996 Oct 17;13(8):1659-65.
Using differential display reverse transcription PCR (DDRT - PCR), we found that a 360 bp cDNA fragment was absent in several c-myc transfected rat fibroblasts: REC:myc, REC:myc + ras and rat1-myc. These cells also showed enhanced sensitivity to gamma ray-induced apoptosis. This cDNA fragment was present in the parental REC (Rat Embryo Cells) and rat1 cells, and in c-Ha-ras transfected REC (REC:ras), all of which were relatively resistant to gamma ray-induced apoptosis. The cDNA fragment was subsequently cloned and used as a probe to screen a rat1 cDNA library, and identified as one of the growth arrest and DNA damaging-inducible genes, gadd153. In addition to the down-regulation of rat gadd153 in all the c-myc transfectants, methyl methanesulfonate (MMS)-induced transcription of the gadd153 was attenuated. The rat1-myc cells, when successfully transfected with and stably expressing the rat gadd153, showed a significantly longer doubling time compared to the parental cells. However, overexpression of gadd153 in rat1-myc cells did not affect gamma ray-induced apoptosis. Thus, the suppression of gadd153 appears to be inversely correlated with that of myc, but not involved in the myc-dependent apoptotic pathway.
利用差异显示逆转录PCR(DDRT-PCR),我们发现一个360bp的cDNA片段在几种转染了c-myc的大鼠成纤维细胞中缺失:REC:myc、REC:myc + ras和rat1-myc。这些细胞对γ射线诱导的凋亡也表现出增强的敏感性。该cDNA片段存在于亲代REC(大鼠胚胎细胞)和rat1细胞以及转染了c-Ha-ras的REC(REC:ras)中,所有这些细胞对γ射线诱导的凋亡都相对具有抗性。随后克隆了该cDNA片段,并用作探针筛选rat1 cDNA文库,鉴定为生长停滞和DNA损伤诱导基因之一,即gadd153。除了在所有c-myc转染子中大鼠gadd153表达下调外,甲磺酸甲酯(MMS)诱导的gadd153转录也减弱。当成功转染并稳定表达大鼠gadd153时,rat1-myc细胞与亲代细胞相比,其倍增时间显著延长。然而,rat1-myc细胞中gadd153的过表达并不影响γ射线诱导的凋亡。因此,gadd153的抑制似乎与myc的抑制呈负相关,但不参与myc依赖的凋亡途径。