EWS/FLI1 up regulates mE2-C, a cyclin-selective ubiquitin conjugating enzyme involved in cyclin B destruction

被引:77
作者
Arvand, A
Bastians, H
Welford, SM
Thompson, AD
Ruderman, JV
Denny, CT [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Calif Los Angeles, Dept Expt Pathol Lab Med, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Pediat, Div Hematol Oncol,Gwynne Hazen Cherry Mem Labs, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
关键词
Ewing's sarcoma; EWS/FLI1; RDA; cell cycle; transformation; E2-C;
D O I
10.1038/sj.onc.1202129
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
The EWS/FLI1 fusion gene found in Ewing's sarcoma and primitive neuroectodermal tumor, is able to transform certain cell lines by acting as an aberrant transcription factor, The ability of EWS/FLI1 to modulate gene expression in cells transformed and resistant to transformation by EWS/FLI1, was assessed by Representational Difference Analysis (RDA), We found that the cyclin selective ubiquitin conjugase murine E2-C, was up regulated in NIH3T3 cells transformed by EWS/FLI1 but not in a nontransformed NIH3T3 clone expressing EWS/FLI1, We also found that mn-C is upregulated in NIH3T3 cells transformed by other genes including activated cdc42, v-ABL and c-myc, We demonstrated that expression of mn-C in both the EWS/FLI1 transformed and parent NIH3T3 lines varies with the cell cycle. Finally, dominant-negative mE2-C, created by changing a catalytic cysteine to serine, inhibits the in vitro ubiquitination and degradation of cyclin B in human HeLa cell extracts. These data suggest that part of the biologic effect of EWS/FLI1 could be, to transcriptionally modulate genes involved in cell cycle regulation.
引用
收藏
页码:2039 / 2045
页数:7
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