Transformation fingerprint: induced STAT3-C, v-Src and Ha-Ras cause small initial changes but similar established profiles in mRNA

被引:24
作者
Paz, K
Socci, ND
van Nimwegen, E
Viale, A
Darnell, JE
机构
[1] Rockefeller Univ, Mol Cell Biol Lab, New York, NY 10021 USA
[2] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[4] Rockefeller Univ, Ctr Studies Phys & Biol, New York, NY 10021 USA
关键词
STAT3-C; Src; transformation;
D O I
10.1038/sj.onc.1207803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Induced transformation of mouse fibroblasts was carried out by releasing tetracycline-repressed expression of an oncogenic mutant of STAT3, STAT3-C, or of v-Src or Ha-Ras. At 15 days after derepression of each oncogene, DNA microarrays showed elevation (> 3-fold) of a similar group of similar to25 mRNAs compared to untransformed cells. RT - PCR confirmed a number of these mRNA elevations. RNA samples were then analysed at intervals during the first 24 h after doxycycline removal to determine the time of early changes. Extensive changes were not observed by array analysis, except in v-Src-expressing cells where about 10 mRNAs were elevated threefold or more. However, RT - PCR did uncover changes in each derepressed cell type that included some of the changes observed after the 15-day transformation period. In addition, STAT3-C target genes such as BclXI and cyclin D1, which were not observed on array analysis, were elevated by RT - PCR analysis. We conclude, therefore, that early after oncogene induction, transcriptional changes, including those initiated by STAT3-C, may occur only in scarce mRNA and/or to a limited extent. However, with additional time and probably additional cell division, a new epigenetic state is established that is mirrored by a changed transcriptional pro. le emblematic of transformation by each of three oncogenes.
引用
收藏
页码:8455 / 8463
页数:9
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