Institute of Pharmaceutical Sciences, ETH Zurich, Switzerland.
Wiley Interdiscip Rev Syst Biol Med. 2010 Mar-Apr;2(2):245-251. doi: 10.1002/wsbm.55.
Some of the classical paradigms of gene regulation have been challenged by global-scale analysis of eukaryotic transcriptional and post-transcriptional gene regulation (PTGR), made possible by the development of genomics and proteomics tools. Post-transcriptional events in particular are increasingly being recognized as important sources of gene regulation. The hundreds of regulatory RNA-binding proteins that exist in eukaryotes may regulate dozens to hundreds of functionally related RNA targets. Likewise, the expression of considerable fractions of many eukaryotic genomes is affected by hundreds of non-coding RNAs, e.g., microRNAs. These findings suggest an enormous regulatory potential for PTGR that may affect virtually every message in a cell. All gene regulatory systems are composed of simple network circuits that coordinate the transfer of regulatory signals to a target gene/message.
真核生物转录和转录后基因调控(PTGR)的全基因组分析对基因调控的经典范例提出了挑战,这得益于基因组学和蛋白质组学工具的发展。特别是转录后事件,越来越被认为是基因调控的重要来源。真核生物中存在数以百计的调控 RNA 结合蛋白,这些蛋白可能调控数十到数百个功能相关的 RNA 靶标。同样,许多真核生物基因组的相当大一部分表达受到数百种非编码 RNA(如 microRNAs)的影响。这些发现表明,PTGR 具有巨大的调控潜力,几乎可以影响细胞中的每一个信息。所有的基因调控系统都是由简单的网络电路组成的,这些电路协调将调控信号传递到靶基因/信息。