Schlosser Isabel, Hölzel Michael, Mürnseer Marlies, Burtscher Helmut, Weidle Ulrich H, Eick Dirk
GSF National Research Centre for Environment and Health, Institute of Clinical Molecular Biology and Tumor Genetics, Marchioninistrasse 25, 81377 Munich, Germany.
Nucleic Acids Res. 2003 Nov 1;31(21):6148-56. doi: 10.1093/nar/gkg794.
The proto-oncogene c-myc encodes a basic helix-loop-helix leucine zipper transcription factor (c-Myc) that has a profound role in growth control and cell cycle progression. Previous microarray studies identified various classes of c-Myc target genes, including genes involved in ribosome biogenesis. By screening the human B-cell line P493-6 and rat fibroblasts conditionally expressing c-Myc, we could substantially extend the list of c-Myc target genes, particularly those required for ribosome biogenesis. The identification of 38 new c-Myc target genes with nucleolar function, prompted us to investigate processing of ribosomal RNA (rRNA). Using pulse-chase labelling experiments we show that c-Myc regulates the efficiency of rRNA maturation. In serum-stimulated P493-6 cells, only the processing of the 47S rRNA precursor to mature 18S and 28S rRNA, but not the synthesis of the 47S transcript, was dependent on the presence of c-Myc. As processing of rRNA is sensitive to inhibition of cyclin-dependent kinase (cdk) activity by roscovitine, we conclude that c-Myc regulates cell growth and proliferation by the coordinated induction of cdk activity and rRNA processing.
原癌基因c-myc编码一种碱性螺旋-环-螺旋亮氨酸拉链转录因子(c-Myc),它在生长控制和细胞周期进程中发挥着重要作用。先前的微阵列研究确定了各类c-Myc靶基因,包括参与核糖体生物合成的基因。通过筛选条件性表达c-Myc的人B细胞系P493-6和大鼠成纤维细胞,我们能够大幅扩充c-Myc靶基因列表,尤其是核糖体生物合成所需的那些基因。38个具有核仁功能的新c-Myc靶基因的鉴定,促使我们研究核糖体RNA(rRNA)的加工过程。通过脉冲追踪标记实验,我们发现c-Myc调节rRNA成熟的效率。在血清刺激的P493-6细胞中,只有47S rRNA前体加工成成熟的18S和28S rRNA依赖于c-Myc的存在,而47S转录本的合成并不依赖。由于rRNA加工对roscovitine抑制细胞周期蛋白依赖性激酶(cdk)活性敏感,我们得出结论,c-Myc通过协同诱导cdk活性和rRNA加工来调节细胞生长和增殖。