HHMI - University of Colorado at Boulder, 347 UCB, Boulder, CO 80309, USA.
Brief Funct Genomics. 2013 Jan;12(1):46-57. doi: 10.1093/bfgp/els058. Epub 2012 Dec 14.
The p53 transcription factor regulates the synthesis of mRNAs encoding proteins involved in diverse cellular stress responses such as cell-cycle arrest, apoptosis, autophagy and senescence. In this review, we discuss how these mRNAs are concurrently regulated at the post-transcriptional level by microRNAs (miRNAs) and RNA-binding proteins (RBPs), which consequently modify the p53 transcriptional program in a cell type- and stimulus-specific manner. We also discuss the action of specific miRNAs and RBPs that are direct transcriptional targets of p53 and how they act coordinately with protein-coding p53 target genes to orchestrate p53-dependent cellular responses.
p53 转录因子调节参与多种细胞应激反应的蛋白质的 mRNA 的合成,如细胞周期停滞、细胞凋亡、自噬和衰老。在这篇综述中,我们讨论了 miRNA(miRNAs)和 RNA 结合蛋白(RBPs)如何在转录后水平上协同调节这些 mRNA,从而以细胞类型和刺激特异性的方式修饰 p53 转录程序。我们还讨论了特定 miRNA 和 RBPs 的作用,这些 miRNA 和 RBPs 是 p53 的直接转录靶标,以及它们如何与编码蛋白质的 p53 靶基因协同作用,协调 p53 依赖性细胞反应。