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Dose-dependent phosphorylation and activation of Hh pathway transcription factors

View ORCID ProfileMengmeng Zhou, Yuhong Han, Bing Wang, Yong Suk Cho, View ORCID ProfileJin Jiang  Correspondence email
Mengmeng Zhou
1Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Roles: Data curation, Formal analysis, Investigation, Writing—review and editing
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  • ORCID record for Mengmeng Zhou
Yuhong Han
1Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Roles: Conceptualization, Data curation, Formal analysis, Investigation, Methodology
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Bing Wang
1Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Roles: Resources, Investigation, Project administration
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Yong Suk Cho
1Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Roles: Data curation, Formal analysis
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Jin Jiang
1Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
2Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Roles: Conceptualization, Formal analysis, Supervision, Funding acquisition, Project administration, Writing—original draft, review, and editing
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  • ORCID record for Jin Jiang
  • For correspondence: jin.jiang@utsouthwestern.edu
Published 5 September 2022. DOI: 10.26508/lsa.202201570
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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.

  • Received June 20, 2022.
  • Revision received August 23, 2022.
  • Accepted August 23, 2022.
  • © 2022 Zhou et al.
Creative Commons logoCreative Commons logohttps://creativecommons.org/licenses/by/4.0/

This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).

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Ci/Gli phosphorylation and activity gradient
Mengmeng Zhou, Yuhong Han, Bing Wang, Yong Suk Cho, Jin Jiang
Life Science Alliance Sep 2022, 5 (11) e202201570; DOI: 10.26508/lsa.202201570

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Ci/Gli phosphorylation and activity gradient
Mengmeng Zhou, Yuhong Han, Bing Wang, Yong Suk Cho, Jin Jiang
Life Science Alliance Sep 2022, 5 (11) e202201570; DOI: 10.26508/lsa.202201570
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Volume 5, No. 11
November 2022
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