RIKEN Center for Biosystems Dynamics Research, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan; Department of Biology, Kobe University Graduate School of Science, Kobe, Hyogo 657-8501, Japan.
RIKEN Center for Biosystems Dynamics Research, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.
Curr Opin Genet Dev. 2020 Aug;63:9-15. doi: 10.1016/j.gde.2020.01.004. Epub 2020 Mar 4.
Receptor tyrosine kinases (RTK) are transmembrane kinases that receive signals for intercellular communication to help organize body plan and sustain tissue homeostasis. These signals converge into the major signaling module of ERK, which transduces signals to the cytoplasm and nucleus. How this module responds to multiple RTK signals, and specifies unique outcomes in each cell, is still poorly understood. Recent technological advances in the quantitative imaging of ERK activity and its manipulation have yielded significant information on the cellular logic behind ERK activation and its readout in the context of Drosophila development. While in the pregastrulation stage, ERK plays a decisive on/off switch; its role changes to modulatory functions of morphogenesis and tissue quality control in the late embryonic stages.
受体酪氨酸激酶 (RTK) 是一种跨膜激酶,它接收细胞间通讯的信号,以帮助组织身体计划并维持组织内稳态。这些信号汇聚到 ERK 的主要信号模块中,该模块将信号转导到细胞质和细胞核中。这个模块如何响应多种 RTK 信号,并在每个细胞中指定独特的结果,仍然知之甚少。ERK 活性的定量成像及其操纵的最新技术进步为 ERK 激活背后的细胞逻辑及其在 Drosophila 发育背景下的读出提供了重要信息。在原肠胚形成阶段,ERK 起着决定性的开/关开关的作用;在胚胎晚期,其作用转变为形态发生和组织质量控制的调节功能。