Integrated Research Institute for Life Sciences, Humboldt-Universität zu Berlin, 10115 Berlin, Germany; email:
Annu Rev Genet. 2017 Nov 27;51:385-411. doi: 10.1146/annurev-genet-120116-023402. Epub 2017 Sep 15.
The question of how noncoding RNAs are involved in Polycomb group (PcG) and Trithorax group (TrxG) regulation has been on an extraordinary journey over the last three decades. Favored models have risen and fallen, and healthy debates have swept back and forth. The field has recently reached a critical mass of compelling data that throws light on several previously unresolved issues. The time is ripe for a fruitful combination of these findings with two other long-running avenues of research, namely the biochemical properties of the PcG/TrxG system and the application of theoretical mathematical models toward an understanding of the system's regulatory properties. I propose that integrating our current knowledge of noncoding RNA into a quantitative biochemical and theoretical framework for PcG and TrxG regulation has the potential to reconcile several apparently conflicting models and identifies fascinating questions for future research.
非编码 RNA 如何参与 Polycomb 组 (PcG) 和 Trithorax 组 (TrxG) 的调控,这个问题在过去的三十年里经历了非凡的探索历程。有优势的模型层出不穷,激烈的争论此起彼伏。该领域最近获得了大量有说服力的数据,这些数据为几个以前尚未解决的问题提供了线索。现在是将这些发现与另外两个长期研究方向(即 PcG/TrxG 系统的生化特性和应用理论数学模型来理解系统的调控特性)进行富有成效的结合的最佳时机。我提出,将我们目前对非编码 RNA 的认识整合到 PcG 和 TrxG 调控的定量生化和理论框架中,有可能调和几个明显相互矛盾的模型,并为未来的研究提出引人入胜的问题。