光体可以实现光敏色素B介导的PIF5降解和稳定的相分离和平衡

Ruth Jean Ae Kim, De Fan, Jiangman He, Keunhwa Kim, Juan Du, Meng Chen
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引用次数: 0

摘要

植物光感受器和热感受器光敏色素B (PHYB)的光激活触发其凝聚成亚核光体(PBs)。然而,PBs的功能仍然令人沮丧地难以捉摸。在这里,我们证明了PHYB缩合使两种拮抗的相分离信号作用共同发生和竞争。我们发现PHYB将光光体色素相互作用因子5 (PIF5)招募到PBs中,并且令人惊讶的是,PHYB在降解和稳定PIF5方面发挥相反的作用。通过过量产生PHYB扰乱PB大小引发双相PIF5反应:而PHYB的适度增加增强了PIF5的降解,进一步提高PHYB水平通过在扩大的PBs中保留更多的PIF5来稳定PIF5。我们的研究结果支持一个模型,其中PHYB冷凝稳定PBs中的PIF5,以抵消PIF5在周围核质中的降解,从而实现对环境敏感的平衡机制来滴定核质PIF5及其转录输出。这种pb激活的信号机制为调节多种植物环境反应中大量与phyb相互作用的信号分子提供了一个框架。我们认为,PBs的这种功能代表了生物分子凝聚物的一般功能,它允许细胞过程或信号通路的不同变化共存并相互作用,从而在单个亚细胞空间内产生动态可调的综合输出。
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Photobodies enable the phase-separation and counterbalance of phytochrome B mediated PIF5 degradation and stabilization
Photoactivation of the plant photoreceptor and thermosensor phytochrome B (PHYB) triggers its condensation into subnuclear photobodies (PBs). However, the function of PBs remains frustratingly elusive. Here, we show that PHYB condensation enables the co-occurrence and competition of two antagonistic phase-separated signaling actions. We found that PHYB recruits PHYTOCHROME-INTERACTING FACTOR5 (PIF5) to PBs and, surprisingly, that PHYB exerts opposing roles in degrading and stabilizing PIF5. Perturbing PB size by overproducing PHYB provoked a biphasic PIF5 response: while a moderate increase in PHYB enhanced PIF5 degradation, further elevating the PHYB level stabilized PIF5 by retaining more of it in enlarged PBs. Our results support a model in which PHYB condensation stabilizes PIF5 in PBs to counteract PIF5 degradation in the surrounding nucleoplasm, thereby enabling an environmentally sensitive counterbalancing mechanism to titrate nucleoplasmic PIF5 and its transcriptional output. This PB-enabled signaling mechanism provides a framework for regulating a plethora of PHYB-interacting signaling molecules in diverse plant environmental responses. We propose that this function of PBs represents a general function of biomolecular condensates to allow distinct variations of a cellular process or signaling pathway to coexist and interact to generate dynamically adjustable integrated outputs within a single subcellular space.
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