Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94158, USA.
Tetrad Graduate Program, University of California San Francisco, San Francisco, CA 94158, USA.
Science. 2023 Jul 21;381(6655):319-324. doi: 10.1126/science.adf4197. Epub 2023 Jun 29.
Unlike other chromatin remodelers, INO80 preferentially mobilizes hexasomes, which can form during transcription. Why INO80 prefers hexasomes over nucleosomes remains unclear. Here, we report structures of INO80 bound to a hexasome or a nucleosome. INO80 binds the two substrates in substantially different orientations. On a hexasome, INO80 places its ATPase subunit, Ino80, at superhelical location -2 (SHL -2), in contrast to SHL -6 and SHL -7, as previously seen on nucleosomes. Our results suggest that INO80 action on hexasomes resembles action by other remodelers on nucleosomes such that Ino80 is maximally active near SHL -2. The SHL -2 position also plays a critical role for nucleosome remodeling by INO80. Overall, the mechanistic adaptations used by INO80 for preferential hexasome sliding imply that subnucleosomal particles play considerable regulatory roles.
与其他染色质重塑因子不同,INO80 优先移动六聚体,六聚体可以在转录过程中形成。为什么 INO80 更喜欢六聚体而不是核小体尚不清楚。在这里,我们报告了 INO80 与六聚体或核小体结合的结构。INO80 以截然不同的取向结合这两种底物。在六聚体上,INO80 将其 ATP 酶亚基 Ino80 置于超螺旋位置-2(SHL-2),与先前在核小体上看到的 SHL-6 和 SHL-7 相反。我们的结果表明,INO80 对六聚体的作用类似于其他重塑因子对核小体的作用,使得 Ino80 在 SHL-2 附近具有最大的活性。SHL-2 位置对于 INO80 引起的核小体重塑也起着关键作用。总的来说,INO80 用于优先六聚体滑动的机制适应性意味着亚核小体颗粒发挥了相当大的调节作用。