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基因毒性应激下p21WAF1/CIP1/SDI1信使核糖核酸与蛋白质表达的解偶联

Uncoupling of p21WAF1/CIP1/SDI1 mRNA and protein expression upon genotoxic stress.

作者信息

Butz K, Geisen C, Ullmann A, Zentgraf H, Hoppe-Seyler F

机构信息

Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

出版信息

Oncogene. 1998 Aug 13;17(6):781-7. doi: 10.1038/sj.onc.1201995.

Abstract

The p21WAF1/CIP1/SDI1 gene is an important regulator of crucial cellular processes, including cell cycle control, cellular differentiation, and the response to genotoxic stress. Induction of p21 gene expression upon DNA damage is widely believed to be p53-dependent. In the present study we analysed the expression of p21 following genotoxic stress, using different DNA-damaging agents and cellular systems. We found that the p21 response markedly varied between different cell lines and also for different genotoxic agents within the same cell line. Genotoxic induction of p21 mRNA expression can occur in the presence of p53-antagonists, such as overexpressed mdm-2 or human papillomavirus (HPV) E6, and in cells harbouring mutated p53 genes. Moreover, upon genotoxic stress, p21 mRNA and protein expression were found to be uncoupled in several cell lines. Thus, transcriptional and postranscriptional changes in p21 expression following DNA damage are not necessarily linked to the intracellular p53 status but strongly depend on the individual cellular background and the type of DNA-damaging agent. Our findings indicate that p21 expression following genotoxic stress underlies a complex control and can be substantially modulated on the posttranscriptional level in a cell-specific manner.

摘要

p21WAF1/CIP1/SDI1基因是关键细胞过程的重要调节因子,包括细胞周期控制、细胞分化以及对基因毒性应激的反应。人们普遍认为,DNA损伤后p21基因表达的诱导是p53依赖性的。在本研究中,我们使用不同的DNA损伤剂和细胞系统,分析了基因毒性应激后p21的表达情况。我们发现,不同细胞系之间以及同一细胞系内不同基因毒性剂作用下,p21的反应存在显著差异。在存在p53拮抗剂(如过表达的mdm-2或人乳头瘤病毒(HPV)E6)的情况下,以及在携带p53基因突变的细胞中,均可发生基因毒性诱导的p21 mRNA表达。此外,在基因毒性应激下,我们发现几个细胞系中p21 mRNA和蛋白质表达是解偶联的。因此,DNA损伤后p21表达的转录和转录后变化不一定与细胞内p53状态相关,而是强烈依赖于个体细胞背景和DNA损伤剂的类型。我们的研究结果表明,基因毒性应激后p21的表达受到复杂的调控,并且在转录后水平上可以以细胞特异性方式受到显著调节。

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