Center for Models of Life, Niels Bohr Institute, University of Copenhagen, Blegdamsvej 17, 2100 Copenhagen Ø, Denmark.
J Mol Biol. 2011 Dec 9;414(4):624-37. doi: 10.1016/j.jmb.2011.10.027. Epub 2011 Oct 20.
Positive feedback in nucleosome modification has been proposed to allow large chromatin regions to exist stably and heritably in distinct expression states. However, modeling has shown that such epigenetic bistability requires that modifying enzymes recruited by nucleosomes are active on distant nucleosomes, potentially allowing uncontrollable spreading of modification. By modeling the silencing of mating-type loci in Saccharomyces cerevisiae, we show that a modification reaction that combines a long-range component and a locally acting component can provide bistability and can be blocked by simple barriers that interrupt the nucleosome chain. We find that robust containment of the silenced region could be achieved by the presence of a number of weak simple barriers in the surrounding chromatin and a limited capacity of the positive feedback reaction. In addition, we show that the state of the silenced region can be regulated by silencer elements acting only on neighboring nucleosomes. Thus, a relatively simple set of nucleosome-modifying enzymes and recognition domains is all that is needed to make chromatin-based epigenetics useful and safe.
核小体修饰中的正反馈被认为可以使大的染色质区域稳定且可遗传地存在于不同的表达状态。然而,建模表明,这种表观遗传双稳态需要被核小体招募的修饰酶在远距离的核小体上具有活性,这可能导致修饰的不可控扩散。通过对酿酒酵母交配型基因座沉默的建模,我们表明,一种修饰反应,结合了远程成分和局部作用成分,可以提供双稳态,并且可以被打断核小体链的简单障碍阻断。我们发现,通过在周围染色质中存在多个弱的简单障碍和正反馈反应的有限能力,可以实现沉默区域的稳健封闭。此外,我们还表明,沉默区域的状态可以通过仅作用于相邻核小体的沉默元件来调节。因此,一组相对简单的核小体修饰酶和识别结构域就足以使基于染色质的表观遗传学变得有用且安全。