The putative apoptosis inhibitor IEX-1L is a mutant nonspliced variant of p22PRG1/IEX-1 and is not expressed in vivo

被引:34
作者
Schäfer, H
Arlt, A
Trauzold, A
Hünermann-Jansen, A
Schmidt, WE
机构
[1] Univ Kiel, Dept Med 1, Lab Mol Gastroenterol Hepatol, Gastrointestinal Unit, D-24105 Kiel, Germany
[2] Ruhr Univ Bochum, St Josef Hosp, Dept Med 1, D-44791 Bochum, Germany
关键词
D O I
10.1006/bbrc.1999.1131
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
IEX-1L has been claimed to act as an apoptosis inhibitor involved in NF kappa B-mediated survival in Jurkat cells [Wu et al. (1998) Science 281, 998-1001], It represents a mutant nonspliced variant of the early response gene p22(PRG1/IEX-1) exhibiting one insertion and two deletions compared to the genomic sequence of p22(PRG/IEX-1). Direct DNA sequencing of PCR products generated from human genomic DNA only detected the regular genomic sequence of p22(PRG1/IEX-1) NO IEX-1L mRNA could be identified by RT-PCR analysis and subsequent DNA sequencing of total, nuclear, or cytoplasmic RNA fractions from PMA-stimulated Jurkat cells. The only functional transcript residing in the cytoplasm is regularly spliced p22(IEX-1/PRG1) mRNA. Substantial amounts of nonmutated nonspliced p22(IEX-1/PRG1) pre-mRNA were identified in the nucleus, Thus, IEX-1L seems to be a mutant variant of p22(IEX-1/PRG1) not existing in vivo. Antiapoptotic effects obviously represent transdominant negative inhibition of endogenous p22(PRG1/IEX-1) in Jurkat cells and several other tumor cell lines. (C) 1999 Academic Press.
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页码:139 / 145
页数:7
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