Transactivation-defective c-MycS retains the ability to regulate proliferation and apoptosis

被引:108
作者
Xiao, QR
Claassen, G
Shi, JY
Adachi, S
Sedivy, J
Hann, SR
机构
[1] Vanderbilt Univ, Sch Med, Dept Cell Biol, Nashville, TN 37232 USA
[2] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
关键词
c-Myc; transactivation; cell cycle; apoptosis; leaky scanning;
D O I
10.1101/gad.12.24.3803
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcriptional activation by c-Myc through specific E box elements is thought to be essential for its biological role. However, c-MycS is unable to activate transcription through these elements and yet retains the ability to stimulate proliferation, induce anchorage-independent growth, and induce apoptosis. In addition, c-MycS retains the ability to repress transcription of several specific promoters. Furthermore, c-MycS can rescue the c-myc null phenotype in fibroblasts with homozygous deletion of c-myc. Taken together, our data argue against the paradigm that all of the biological functions of c-Myc are mediated by transcriptional activation of specific target genes through E box elements.
引用
收藏
页码:3803 / 3808
页数:6
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