Identification of c-Myc responsive genes using rat cDNA microarray

被引:2
|
作者
Guo, QM
Malek, RL
Kim, S
Chiao, C
He, M
Ruffy, M
Sanka, K
Lee, NH
Dang, CV
Liu, ET
机构
[1] NCI, Div Clin Sci, Med Branch, Dept Canc & Cell Biol,Mol Signaling & Oncogenesis, Bethesda, MD 20892 USA
[2] Inst Genomic Res, Dept Cellular & Mol Biol, Rockville, MD 20850 USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Hematol, Baltimore, MD 21205 USA
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
c-Myc functions; through direct activation or repression of transcription. Using cDNA microarray analysis, we have identified c-Mj c-responsive genes by comparing gene expression profiles between c-myc null and c-myc wildtype rat fibroblast cells and between c-myc null and c-myc nub cells reconstituted with c-myc. From a panel of 4400 cDNA elements, we found 198 genes responsive to c-myc when comparing wild-type or reconstituted cells with the null cells. The plurality of the named c-Myc-responsive genes that were up-regulated, including 30 ribosomal protein genes, are involved in macromolecular synthesis and metabolism, suggesting a major role of c-Myc in the regulation of protein synthetic and metabolic pathways. When ectopically overexpressed, c-Myc induced a different and smaller set of c-Myc-responsive genes as compared with the physiologically expressed c-Myc condition. Thus, these results from expression profiling suggest a new primary function for c-Myc and raise the possibility that the physiological and transforming functions of c-myc may be separable.
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收藏
页码:5922 / 5928
页数:7
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