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刺猬信号转导中的磷酸化密码

Gli Phosphorylation Code in Hedgehog Signal Transduction.

作者信息

Zhou Mengmeng, Jiang Jin

机构信息

Department of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, United States.

Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX, United States.

出版信息

Front Cell Dev Biol. 2022 Jan 25;10:846927. doi: 10.3389/fcell.2022.846927. eCollection 2022.

DOI:10.3389/fcell.2022.846927
PMID:35186941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8855225/
Abstract

Hedgehog (Hh) family of secreted proteins governs many key processes in embryonic development and adult tissue homeostasis in species ranging from insects to human. Deregulation of Hh signaling has been implicated in a wide range of human diseases including birth defect and cancer. Hh signaling pathway culminates in the conversion of the latent transcription factor Cubitus interruptus (Ci)/Gli from a repressor form (Ci/Gli) into an activator form (Ci/Gli). Both the production of Ci/Gli in the absence of Hh and the formation of Ci/Gli in response to Hh are regulated by phosphorylation. Whereas previous studies demonstrated that sequential phosphorylation by protein kinase A (PKA), glycogen synthase kinase 3 (GSK3), and casein kinase 1 (CK1) at multiple Ser/Thr clusters in the C-terminal region of Ci/Gli targets it for proteolytic processing to generate Ci/Gli, recent studies revealed that phosphorylation of Ci/Gli by the Fused (Fu)/Unc-51 like kinase (Ulk) family kinases Fu/Ulk3/Stk36 and other kinases contributes to Ci/Gli activation. Fu/Ulk3/Stk36-mediated phosphorylation of Ci/Gli is stimulated by Hh, leading to altered interaction between Ci/Gli and the Hh pathway repressor Sufu. Here we review our current understanding of how various Ci/Gli phosphorylation events are regulated and how they influence Hh signal transduction.

摘要

刺猬(Hh)家族分泌蛋白在从昆虫到人类等多种物种的胚胎发育和成年组织稳态中调控着许多关键过程。Hh信号通路失调与包括出生缺陷和癌症在内的多种人类疾病有关。Hh信号通路最终导致潜在转录因子间断性肘脉(Ci)/Gli从阻遏形式(Ci/Gli)转变为激活形式(Ci/Gli)。在没有Hh时Ci/Gli的产生以及对Hh响应时Ci/Gli的形成均受磷酸化调控。尽管先前的研究表明,蛋白激酶A(PKA)、糖原合酶激酶3(GSK3)和酪蛋白激酶1(CK1)在Ci/Gli C末端区域的多个丝氨酸/苏氨酸簇上进行的顺序磷酸化将其靶向进行蛋白水解加工以产生Ci/Gli,但最近的研究表明,融合(Fu)/Unc-51样激酶(Ulk)家族激酶Fu/Ulk3/Stk36和其他激酶对Ci/Gli的磷酸化有助于Ci/Gli的激活。Hh刺激Fu/Ulk3/Stk36介导的Ci/Gli磷酸化,导致Ci/Gli与Hh信号通路阻遏物Sufu之间的相互作用发生改变。在此,我们综述了目前对各种Ci/Gli磷酸化事件如何被调控以及它们如何影响Hh信号转导的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e491/8855225/80d467c63830/fcell-10-846927-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e491/8855225/3e337c787bbb/fcell-10-846927-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e491/8855225/80d467c63830/fcell-10-846927-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e491/8855225/3e337c787bbb/fcell-10-846927-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e491/8855225/80d467c63830/fcell-10-846927-g002.jpg

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