Rudolph B, Saffrich R, Zwicker J, Henglein B, Müller R, Ansorge W, Eilers M
Zentrum für Molekulare Biologie Heidelberg (ZMBH), Germany.
EMBO J. 1996 Jun 17;15(12):3065-76.
The activation of conditional alleles of Myc induces both cell proliferation and apoptosis in serum-deprived RAT1 fibroblasts. Entry into S phase and apoptosis are both preceded by increased levels of cyclin E- and cyclin D1-dependent kinase activities. To assess which, if any, cellular responses to Myc depend on active cyclin-dependent kinases (cdks), we have microinjected expression plasmids encoding the cdk inhibitors p16, p21 or p27, and have used a specific inhibitor of cdk2, roscovitine. Expression of cyclin A, which starts late in G1 phase, served as a marker for cell cycle progression. Our data show that active G1 cyclin/cdk complexes are both necessary and sufficient for induction of cyclin A by Myc. In contrast, neither microinjection of cdk inhibitors nor chemical inhibition of cdk2 affected the ability of Myc to induce apoptosis in serum-starved cells. Further, in isoleucine-deprived cells, Myc induces apoptosis without altering cdk activity. We conclude that Myc acts upstream of cdks in stimulating cell proliferation and also that activation of cdks and induction of apoptosis are largely independent events that occur in response to induction of Myc.
Myc条件等位基因的激活在血清饥饿的RAT1成纤维细胞中既诱导细胞增殖又诱导细胞凋亡。进入S期和凋亡之前,细胞周期蛋白E和细胞周期蛋白D1依赖性激酶活性水平均升高。为了评估对Myc的哪些细胞反应(如果有的话)依赖于活性细胞周期蛋白依赖性激酶(cdk),我们显微注射了编码cdk抑制剂p16、p21或p27的表达质粒,并使用了cdk2的特异性抑制剂roscovitine。在G1期晚期开始表达的细胞周期蛋白A用作细胞周期进程的标志物。我们的数据表明,活性G1细胞周期蛋白/cdk复合物对于Myc诱导细胞周期蛋白A既必要又充分。相反,显微注射cdk抑制剂或化学抑制cdk2均不影响Myc在血清饥饿细胞中诱导凋亡的能力。此外,在异亮氨酸缺乏的细胞中,Myc诱导凋亡而不改变cdk活性。我们得出结论,Myc在刺激细胞增殖中作用于cdk的上游,并且cdk的激活和凋亡的诱导在很大程度上是响应于Myc诱导而发生的独立事件。