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形态发生素诱导的激酶凝聚物通过变构激活Gli来转导Hh信号。

Morphogen-induced kinase condensates transduce Hh signal by allosterically activating Gli.

作者信息

Han Yuhong, Zhou Mengmeng, Wang Bing, Jiang Jin

机构信息

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

Sci Adv. 2025 Jan 10;11(2):eadq1790. doi: 10.1126/sciadv.adq1790.

Abstract

Hedgehog (Hh) morphogen governs embryonic development and tissue homeostasis through the Ci/Gli family transcription factors. Here we report that Hh induces phase separation of the fused (Fu)/Ulk family kinases to allosterically regulate Ci/Gli. We find that Hh-induced phosphorylation of Fu/Ulk3 promotes SUMOylation of their inverted phosphorylation-dependent SUMOylation motifs. Subsequent interaction between SUMO and SUMO-interacting motif drives Fu/Ulk3 self-assembly to form biomolecular condensates that recruit Ci-Sufu and Gli-Sufu in the cytoplasm and primary cilium, respectively. Within the condensates, Fu/Ulk3 undergoes a conformational change to expose Ci/Gli for Fu/Ulk3-mediated phosphorylation and activation, leading to gradual accumulation of nuclear Ci/Gli transcriptional complexes in proportion to ligand dose and exposure time. Our findings provide mechanistic insights into the spatiotemporal control of Hh signal transduction, reveal previously unexplored regulatory mechanism and function for biomolecular condensation, and establish a paradigm for kinase-mediated signal transduction whereby a kinase allosterically activates its substrate through ligand-induced and condensation-driven conformational change.

摘要

刺猬蛋白(Hh)形态发生素通过Ci/Gli家族转录因子调控胚胎发育和组织稳态。在此我们报告,Hh诱导融合(Fu)/Ulk家族激酶发生相分离,以变构方式调节Ci/Gli。我们发现,Hh诱导的Fu/Ulk3磷酸化促进其反向磷酸化依赖性SUMO化基序的SUMO化。SUMO与SUMO相互作用基序之间的后续相互作用驱动Fu/Ulk3自组装,形成生物分子凝聚物,分别在细胞质和初级纤毛中招募Ci-Sufu和Gli-Sufu。在凝聚物中,Fu/Ulk3发生构象变化,使Ci/Gli暴露,以便Fu/Ulk3介导磷酸化和激活,导致核Ci/Gli转录复合物与配体剂量和暴露时间成比例地逐渐积累。我们的研究结果为Hh信号转导的时空控制提供了机制见解,揭示了生物分子凝聚此前未被探索的调节机制和功能,并建立了一种激酶介导的信号转导模式,即激酶通过配体诱导和凝聚驱动的构象变化变构激活其底物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ff/11721587/54e5f568e0d3/sciadv.adq1790-f1.jpg

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