Division of Chromatin Networks, German Cancer Research Center (DKFZ) and BioQuant, Im Neuenheimer Feld 280, Heidelberg, 69120, Germany.
Bioessays. 2017 Dec;39(12). doi: 10.1002/bies.201700053. Epub 2017 Oct 16.
Nucleosomes "talk" to each other about their modification state to form extended domains of modified histones independently of the underlying DNA sequence. At the same time, DNA elements promote modification of nucleosomes in their vicinity. How do these site-specific and histone-based activities act together to regulate spreading of histone modifications along the genome? How do they enable epigenetic memory to preserve cell identity? Many models for the dynamics of repressive histone modifications emphasize the role of strong positive feedback loops, which reinforce histone modifications by recruiting histone modifiers to preexisting modifications. Recent experiments question that repressive histone modifications are self-sustained independently of their genomic context, thereby indicating that histone-based feedback is relatively weak. In the present review, current models for the dynamics of histone modifications are compared and it is suggested that limitation of histone-based feedback is key to intrinsic confinement of spreading and coexistence of short- and long-term memory at different genomic loci. See also the video abstract here: https://youtu.be/3bxr_xDEZfQ.
核小体“彼此交谈”,讨论其修饰状态,从而在不依赖于基础 DNA 序列的情况下形成修饰组蛋白的扩展域。同时,DNA 元件促进其附近核小体的修饰。这些基于特定位置和组蛋白的活性如何共同作用以调节组蛋白修饰沿着基因组的扩散?它们如何使表观遗传记忆能够维持细胞身份?许多关于抑制性组蛋白修饰动态的模型强调了强正反馈环的作用,该反馈环通过将组蛋白修饰酶招募到预先存在的修饰上来增强组蛋白修饰。最近的实验对抑制性组蛋白修饰是否独立于其基因组背景而自我维持提出了质疑,从而表明基于组蛋白的反馈相对较弱。在本综述中,比较了组蛋白修饰动态的现有模型,并提出了基于组蛋白的反馈的限制是内在限制扩散以及在不同基因组位置共存短期和长期记忆的关键。也可在此处查看视频摘要:https://youtu.be/3bxr_xDEZfQ。