Hoang A T, Cohen K J, Barrett J F, Bergstrom D A, Dang C V
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6875-9. doi: 10.1073/pnas.91.15.6875.
The involvement of c-Myc in cellular proliferation or apoptosis has been linked to differential cyclin gene expression. We observed that in both proliferating cells and cells undergoing apoptosis, cyclin A (but not B, C, D1, and E) mRNA level was elevated in unsynchronized Myc-overexpressing cells when compared with parental Rat1a fibroblasts. We further demonstrated that Zn(2+)-inducible cyclin A expression was sufficient to cause apoptosis. When Myc-induced apoptosis was blocked by coexpression of Bcl-2, the levels of cyclin C, D1, and E mRNAs were also elevated. Thus, while apoptosis induced by c-Myc is associated with an elevated cyclin A mRNA level, protection from apoptosis by coexpressed Bcl-2 is associated with a complementary increase in cyclin C, D1, and E mRNAs.
c-Myc参与细胞增殖或凋亡与细胞周期蛋白基因的差异表达有关。我们观察到,与亲代Rat1a成纤维细胞相比,在增殖细胞和正在经历凋亡的细胞中,未同步化的Myc过表达细胞中细胞周期蛋白A(而非B、C、D1和E)的mRNA水平均升高。我们进一步证明,锌离子诱导的细胞周期蛋白A表达足以导致凋亡。当通过共表达Bcl-2阻断Myc诱导的凋亡时,细胞周期蛋白C、D1和E的mRNA水平也会升高。因此,虽然c-Myc诱导的凋亡与细胞周期蛋白A的mRNA水平升高有关,但共表达的Bcl-2对凋亡的保护作用与细胞周期蛋白C、D1和E的mRNA的互补性增加有关。