Transcriptional Amplification in Tumor Cells with Elevated c-Myc

被引:1343
作者
Lin, Charles Y. [1 ,2 ]
Loven, Jakob [1 ]
Rahl, Peter B. [1 ]
Paranal, Ronald M. [4 ]
Burge, Christopher B. [3 ]
Bradner, James E. [4 ,5 ]
Lee, Tong Ihn [1 ]
Young, Richard A. [1 ,3 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Computat & Syst Biol Program, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[5] Harvard Univ, Dept Med, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
RECRUITS P-TEFB; GENE-EXPRESSION; NEOPLASTIC PHENOTYPE; RIBOSOMAL DNA; COPY-NUMBER; CANCER; MAX; BINDING; ACTIVATION; PROTEIN;
D O I
10.1016/j.cell.2012.08.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Elevated expression of the c-Myc transcription factor occurs frequently in human cancers and is associated with tumor aggression and poor clinical outcome. The effect of high levels of c-Myc on global gene regulation is poorly understood but is widely thought to involve newly activated or repressed "Myc target genes." We report here that in tumor cells expressing high levels of c-Myc the transcription factor accumulates in the promoter regions of active genes and causes transcriptional amplification, producing increased levels of transcripts within the cell's gene expression program. Thus, rather than binding and regulating a new set of genes, c-Myc amplifies the output of the existing gene expression program. These results provide an explanation for the diverse effects of oncogenic c-Myc on gene expression in different tumor cells and suggest that transcriptional amplification reduces rate-limiting constraints for tumor cell growth and proliferation.
引用
收藏
页码:56 / 67
页数:12
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