Marhin W W, Chen S, Facchini L M, Fornace A J, Penn L Z
Department of Molecular and Medical Genetics, University of Toronto, Ontario Cancer Institute, Canada.
Oncogene. 1997 Jun 12;14(23):2825-34. doi: 10.1038/sj.onc.1201138.
The c-Myc protein strongly stimulates cellular proliferation, inducing cells to exit G0/G1 and enter the cell cycle. At a molecular level, Myc prevents growth arrest and drives cell cycle progression through the transcriptional regulation of Myc-target genes. Expression of the growth arrest and DNA damage inducible gene 45 (gadd45) is elevated in response to DNA damaging agents, such as ionizing radiation via a p53-dependent mechanism, upon nutrient deprivation, or during differentiation. Gadd45 holds a vital role in growth arrest as ectopic expression confers a strong block to proliferation. Exposure of quiescent cells to mitogen stimulates a rapid increase in c-Myc expression which is followed by the subsequent reduction in gadd45 expression. The kinetics of these two regulatory events suggest that Myc suppresses the expression of gadd45, contributing to G0/G1 phase exit of the cell cycle. Indeed, ectopic Myc expression in primary and immortalized fibroblasts results in the suppression of gadd45 mRNA levels, by a mechanism which is independent of cell cycle progression. Using an inducible MycER system, rapid suppression of gadd45 mRNA is first evident approximately 0.5 h following Myc activation. The reduction in gadd45 mRNA expression occurs at the transcriptional level and is mediated by a p53-independent pathway. Moreover, Myc suppression and p53 induction of gadd45 following exposure to ionizing radiation are non-competitive co-regulatory events. Myc suppression of gadd45 defines a novel pathway through which Myc promotes cell cycle entry and prevents growth arrest of transformed cells.
c-Myc蛋白强烈刺激细胞增殖,诱导细胞退出G0/G1期并进入细胞周期。在分子水平上,Myc通过对Myc靶基因的转录调控来阻止生长停滞并驱动细胞周期进程。生长停滞和DNA损伤诱导基因45(gadd45)的表达在响应DNA损伤剂(如通过p53依赖机制的电离辐射)、营养剥夺或分化过程中会升高。Gadd45在生长停滞中起着至关重要的作用,因为异位表达会强烈阻止增殖。将静止细胞暴露于有丝分裂原会刺激c-Myc表达迅速增加,随后gadd45表达降低。这两个调节事件的动力学表明,Myc抑制gadd45的表达,促使细胞周期退出G0/G1期。事实上,在原代和成永生化成纤维细胞中异位表达Myc会导致gadd45 mRNA水平受到抑制,其机制独立于细胞周期进程。使用诱导型MycER系统,在Myc激活后约0.5小时,gadd45 mRNA的快速抑制首先变得明显。gadd45 mRNA表达的降低发生在转录水平,并且由p53非依赖途径介导。此外,暴露于电离辐射后,Myc对gadd45的抑制和p53对gadd45的诱导是不相互竞争的共同调节事件。Myc对gadd45的抑制定义了一条新的途径,通过该途径Myc促进细胞周期进入并防止转化细胞的生长停滞。