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剂量依赖性磷酸化和 HH 通路转录因子的激活。

Dose-dependent phosphorylation and activation of Hh pathway transcription factors.

机构信息

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

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

出版信息

Life Sci Alliance. 2022 Sep 5;5(11). doi: 10.26508/lsa.202201570. Print 2022 Nov.

Abstract

Graded Hedgehog (Hh) signaling is mediated by graded Cubitus interruptus (Ci)/Gli transcriptional activity, but how the Hh gradient is converted into the Ci/Gli activity gradient remains poorly understood. Here, we show that graded Hh induces a progressive increase in Ci phosphorylation at multiple Fused (Fu)/CK1 sites including a cluster located in the C-terminal Sufu-binding domain. We demonstrated that Fu directly phosphorylated Ci on S1382, priming CK1 phosphorylation on adjacent sites, and that Fu/CK1-mediated phosphorylation of the C-terminal sites interfered with Sufu binding and facilitated Ci activation. Phosphorylation at the N-terminal, middle, and C-terminal Fu/CK1 sites occurred independently of one another and each increased progressively in response to increasing levels of Hh or increasing amounts of Hh exposure time. Increasing the number of phospho-mimetic mutations of Fu/CK1 sites resulted in progressively increased Ci activation by alleviating Sufu-mediated inhibition. We found that the C-terminal Fu/CK1 phosphorylation cluster is conserved in Gli2 and contributes to its dose-dependent activation. Our study suggests that the Hh signaling gradient is translated into a Ci/Gli phosphorylation gradient that activates Ci/Gli by gradually releasing Sufu-mediated inhibition.

摘要

级联的 Hedgehog(Hh)信号转导是由级联 Cubitus interruptus(Ci)/Gli 转录活性介导的,但 Hh 梯度如何转化为 Ci/Gli 活性梯度仍知之甚少。在这里,我们表明,梯度 Hh 诱导 Ci 在多个 Fused(Fu)/CK1 位点上的磷酸化逐渐增加,包括位于 C 末端 Sufu 结合域中的一个簇。我们证明 Fu 直接在 S1382 上磷酸化 Ci,为 CK1 在相邻位点上的磷酸化做准备,并且 Fu/CK1 介导的 C 末端位点的磷酸化干扰 Sufu 结合并促进 Ci 的激活。N 端、中间和 C 端 Fu/CK1 位点的磷酸化彼此独立发生,并且随着 Hh 水平的增加或 Hh 暴露时间的增加而逐渐增加。增加 Fu/CK1 磷酸化位点的磷酸模拟突变数量会通过减轻 Sufu 介导的抑制来导致 Ci 激活逐渐增加。我们发现,Gli2 中保守的 C 末端 Fu/CK1 磷酸化簇有助于其剂量依赖性激活。我们的研究表明,Hh 信号梯度被转化为 Ci/Gli 磷酸化梯度,通过逐渐释放 Sufu 介导的抑制来激活 Ci/Gli。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b45e/9445324/c8db6910d50f/LSA-2022-01570_Fig1.jpg

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