Amundson S A, Zhan Q, Penn L Z, Fornace A J
NCI, NIH, Bethesda, Maryland 20892, USA.
Oncogene. 1998 Oct 29;17(17):2149-54. doi: 10.1038/sj.onc.1202136.
The growth arrest and DNA damage inducible (gadd) genes are induced by various genotoxic and non-genotoxic stresses such as serum starvation, ultraviolet irradiation and treatment with alkylating agents. Their coordinate induction is a growth arrest signal which may play an important role in the response of cells to DNA damage. Conversely, c-myc is a strong proliferative signal, and overexpression of Myc is frequently observed in cancer cells. We have found that ectopic expression of v-myc in RAT-1 cells results in an attenuated induction of the three major gadd transcripts by methyl methanesulfonate (MMS), and almost completely blocks the response to ultraviolet (UV) radiation. Myc acts in part by reducing the stress-responsiveness of the gadd45 promoter, as a c-myc expression vector strongly suppressed activation of gadd45-reporter constructs. This activity of Myc localizes to a recently described GC-rich binding site within the gadd45 promoter. These results indicate that a coordinate down-regulation of the gadd gene response is one mechanism by which Myc can circumvent growth arrest and contribute to the neoplastic phenotype.
生长停滞和DNA损伤诱导(gadd)基因可被多种基因毒性和非基因毒性应激所诱导,如血清饥饿、紫外线照射以及用烷化剂处理。它们的协同诱导是一种生长停滞信号,可能在细胞对DNA损伤的反应中起重要作用。相反,c-myc是一种强大的增殖信号,Myc的过表达在癌细胞中经常可见。我们发现,在RAT-1细胞中异位表达v-myc会导致甲磺酸甲酯(MMS)对三种主要gadd转录本的诱导减弱,并且几乎完全阻断对紫外线(UV)辐射的反应。Myc部分通过降低gadd45启动子的应激反应性发挥作用,因为c-myc表达载体强烈抑制gadd45报告基因构建体的激活。Myc的这种活性定位于gadd45启动子内最近描述的富含GC的结合位点。这些结果表明,gadd基因反应的协同下调是Myc能够规避生长停滞并促成肿瘤表型的一种机制。