Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA.
Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA; Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA; Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093, USA.
Mol Cell. 2021 Oct 21;81(20):4137-4146. doi: 10.1016/j.molcel.2021.09.010. Epub 2021 Oct 6.
Cell signaling is a complex process. The faithful transduction of information into specific cellular actions depends on the synergistic effects of many regulatory molecules, nurtured by their strict spatiotemporal regulation. Over the years, we have gained copious insights into the subcellular architecture supporting this spatiotemporal control, including the roles of membrane-bound organelles and various signaling nanodomains. Recently, liquid-liquid phase separation (LLPS) has been recognized as another potentially ubiquitous framework for organizing signaling molecules with high specificity and precise spatiotemporal control in cells. Here, we review the pervasive role of LLPS in signal transduction, highlighting several key pathways that intersect with LLPS, including examples in which LLPS is controlled by signaling events. We also examine how LLPS orchestrates signaling by compartmentalizing signaling molecules, amplifying signals non-linearly, and moderating signaling dynamics. We focus on the specific molecules that drive LLPS and highlight the known functional and pathological consequences of LLPS in each pathway.
细胞信号转导是一个复杂的过程。信息被准确地转导为特定的细胞反应,这依赖于许多调节分子的协同作用,并受到其严格的时空调节的滋养。多年来,我们深入了解了支持这种时空控制的亚细胞结构,包括膜结合细胞器和各种信号纳米域的作用。最近,液-液相分离(LLPS)已被认为是另一种具有高特异性和精确时空控制的组织信号分子的潜在普遍框架。在这里,我们综述了 LLPS 在信号转导中的普遍作用,强调了与 LLPS 交叉的几个关键途径,包括由信号事件控制的 LLPS 的例子。我们还研究了 LLPS 如何通过分隔信号分子、非线性放大信号以及调节信号动力学来协调信号。我们专注于驱动 LLPS 的特定分子,并强调每个途径中 LLPS 的已知功能和病理后果。