Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United States.
Tetrad Graduate Program, University of California, San Francisco, San Francisco, United States.
Elife. 2018 Apr 17;7:e35322. doi: 10.7554/eLife.35322.
ISWI family chromatin remodeling motors use sophisticated autoinhibition mechanisms to control nucleosome sliding. Yet how the different autoinhibitory domains are regulated is not well understood. Here we show that an acidic patch formed by histones H2A and H2B of the nucleosome relieves the autoinhibition imposed by the AutoN and the NegC regions of the human ISWI remodeler SNF2h. Further, by single molecule FRET we show that the acidic patch helps control the distance travelled per translocation event. We propose a model in which the acidic patch activates SNF2h by providing a landing pad for the NegC and AutoN auto-inhibitory domains. Interestingly, the INO80 complex is also strongly dependent on the acidic patch for nucleosome sliding, indicating that this substrate feature can regulate remodeling enzymes with substantially different mechanisms. We therefore hypothesize that regulating access to the acidic patch of the nucleosome plays a key role in coordinating the activities of different remodelers in the cell.
ISWI 家族染色质重塑马达利用复杂的自动抑制机制来控制核小体滑动。然而,不同的自动抑制结构域是如何被调控的还不是很清楚。在这里,我们发现核小体中的组蛋白 H2A 和 H2B 形成的酸性斑解除了人源 ISWI 重塑酶 SNF2h 的 AutoN 和 NegC 区域施加的自动抑制。此外,通过单分子 FRET,我们发现酸性斑有助于控制每次转位事件所移动的距离。我们提出了一个模型,其中酸性斑通过为 NegC 和 AutoN 自动抑制结构域提供一个着陆点来激活 SNF2h。有趣的是,INO80 复合物对于核小体滑动也强烈依赖于酸性斑,这表明这种底物特征可以调节具有截然不同机制的重塑酶。因此,我们假设调节对核小体酸性斑的访问在协调细胞中不同重塑酶的活性方面起着关键作用。