ETH Zurich, Zurich, Switzerland.
University of California, Berkeley, Berkeley, United States.
Elife. 2019 Jan 16;8:e41415. doi: 10.7554/eLife.41415.
Processing bodies (PBs) are cytoplasmic mRNP granules that assemble via liquid-liquid phase separation and are implicated in the decay or storage of mRNAs. How PB assembly is regulated in cells remains unclear. Previously, we identified the ATPase activity of the DEAD-box protein Dhh1 as a key regulator of PB dynamics and demonstrated that Not1, an activator of the Dhh1 ATPase and member of the CCR4-NOT deadenylase complex inhibits PB assembly (Mugler et al., 2016). Here, we show that the PB component Pat1 antagonizes Not1 and promotes PB assembly via its direct interaction with Dhh1. Intriguingly, PB dynamics can be recapitulated , since Pat1 enhances the phase separation of Dhh1 and RNA into liquid droplets, whereas Not1 reverses Pat1-Dhh1-RNA condensation. Overall, our results uncover a function of Pat1 in promoting the multimerization of Dhh1 on mRNA, thereby aiding the assembly of large multivalent mRNP granules that are PBs.
胞质多聚体 (PBs) 是通过液-液相分离组装的细胞质 mRNP 颗粒,与 mRNAs 的降解或储存有关。细胞中 PB 组装如何受到调控仍不清楚。先前,我们鉴定了 DEAD 盒蛋白 Dhh1 的 ATP 酶活性是 PB 动力学的关键调节因子,并证明了 Not1,一种 Dhh1 ATP 酶的激活剂和 CCR4-NOT 脱腺苷酸化酶复合物的成员,抑制 PB 组装 (Mugler 等人,2016)。在这里,我们表明 PB 成分 Pat1 通过与 Dhh1 的直接相互作用拮抗 Not1 并促进 PB 组装。有趣的是,PB 动力学可以被再现,因为 Pat1 增强了 Dhh1 和 RNA 进入液滴的相分离,而 Not1 逆转了 Pat1-Dhh1-RNA 的凝聚。总的来说,我们的结果揭示了 Pat1 在促进 Dhh1 在 mRNA 上的多聚化从而辅助大的多价 mRNP 颗粒(即 PBs)组装方面的功能。