Apoptosis mediated by a novel leucine zipper protein Par-4

被引:31
作者
Rangnekar, VM
机构
[1] Univ Kentucky, Grad Ctr Toxicol, Dept Surg, Lexington, KY 40536 USA
[2] Univ Kentucky, Grad Ctr Toxicol, Dept Microbiol & Immunol, Lexington, KY 40536 USA
[3] Univ Kentucky, Lucille P Markey Canc Ctr, Lexington, KY 40536 USA
关键词
apoptosis; Par-4; prostate;
D O I
10.1023/A:1009666705875
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 prostate apoptosis response-4 (par-4) gene was isolated in a differential screen for immediate-early genes that are up-regulated during apoptosis of prostate cancer cells, Unlike most other immediate-early genes, par-4 is exclusively induced during apoptosis, The expression or induction of par-4 is not restricted to prostatic cells. The par-4 gene is widely expressed in diverse normal tissues and cell types and conserved during evolution. Par-4 protein contains a leucine zipper domain that is essential for sensitization of cells to apoptosis, Functional studies indicate that par-4 expression is necessary to induce apoptosis, Par-4 protein may induce apoptosis by a p53-independent pathway that involves cytoplasmic inactivation of atypical protein kinase C isoforms resulting in down-regulation of MAP kinase activity and an up-regulation of p38 kinase activity. However, Par-4 is detected in the cytoplasm and in the nucleus, suggesting both cytoplasmic and nuclear roles for the pro-apoptotic protein, Interestingly, Par-4 is predicted to contain a death domain homologous to that of Fas or TRADD, and may therefore trigger a death cascade analogous to that of the death domain proteins, Par-4-dependent apoptosis is abrogated by Bcl-2 and by caspase inhibitors. Identification of the components of the p53-independent apoptosis pathway induced by Par-4 may help to further elucidate the mechanism of Par-4 action. Moreover, in view of the pro-apoptotic function of Par-4, its role in diseases, such as cancer and neurogenerative disorders, whose pathophysiology involves apoptotic cell death needs further investigation.
引用
收藏
页码:61 / 66
页数:6
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