Identification and cloning of EI24, a gene induced by p53 in etoposide-treated cells

被引:3
|
作者
Lehar, SM
Naeht, M
Jacks, T
Vater, CA
Chittenden, T
Guild, BC
机构
[1] APOPTOSIS TECHNOL INC,CAMBRIDGE,MA 02139
[2] MIT,CTR CANC RES,HOWARD HUGHES MED INST,CAMBRIDGE,MA 02139
关键词
p53; gene induction; differential display; apoptosis;
D O I
暂无
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
To search for candidate genes involved in p53-mediated apoptosis, the differential display technique was used to identify RNA species whose expression was altered in murine NIH3T3 cells treated with the cytotoxic drug etoposide. We report here the isolation and characterization of EI24, a novel gene whose 2.4 kb mRNA is induced following etoposide treatment. Induction of EI24 mRNA by etoposide required expression of wild-type p53 in murine embryonic fibroblasts which had been transformed with the oncogenes E1A and T24 H-ras; and overexpression of functional p53 in these cells was sufficient to induce expression of the EI24 mRNA. The EI24 mRNA was also induced in a p53-dependent manner by ionizing irradiation of primary murine thymocytes. Isolation of a full-length EI24 cDNA revealed that its protein product bears homology to CELF37C12.2, a Caenorhabditis elegans protein of unknown function.
引用
收藏
页码:1181 / 1187
页数:7
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