A Huluwa phosphorylation switch regulates embryonic axis induction

Abstract Embryonic axis formation is essential for patterning and morphogenesis in vertebrates and is tightly regulated by the dorsal organizer. Previously, we demonstrated that maternally derived Huluwa (Hwa) acts as a dorsal determinant, dictating axis formation by activating β-catenin signaling i...

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Main Authors: Yao Li, Yun Yan, Bo Gong, Qianwen Zheng, Haiyan Zhou, Jiarui Sun, Mingpeng Li, Zhao Wang, Yaohui Li, Yunjing Wan, Weixi Chen, Shiqian Qi, Xianming Mo, Anming Meng, Bo Xiang, Jing Chen
Format: Article
Language:English
Published: Nature Portfolio 2024-11-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-54450-4
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author Yao Li
Yun Yan
Bo Gong
Qianwen Zheng
Haiyan Zhou
Jiarui Sun
Mingpeng Li
Zhao Wang
Yaohui Li
Yunjing Wan
Weixi Chen
Shiqian Qi
Xianming Mo
Anming Meng
Bo Xiang
Jing Chen
author_facet Yao Li
Yun Yan
Bo Gong
Qianwen Zheng
Haiyan Zhou
Jiarui Sun
Mingpeng Li
Zhao Wang
Yaohui Li
Yunjing Wan
Weixi Chen
Shiqian Qi
Xianming Mo
Anming Meng
Bo Xiang
Jing Chen
author_sort Yao Li
collection DOAJ
description Abstract Embryonic axis formation is essential for patterning and morphogenesis in vertebrates and is tightly regulated by the dorsal organizer. Previously, we demonstrated that maternally derived Huluwa (Hwa) acts as a dorsal determinant, dictating axis formation by activating β-catenin signaling in zebrafish and Xenopus. However, the mechanism of activation and fine regulation of the Hwa protein remains unclear. Through candidate screening we identified a mutation at Ser168 in the PPNSP motif of Hwa that dramatically abolishes its axis-inducing activity. Mechanistically, mutating the Ser168 residue reduced its binding affinity to Tankyrase 1/2 and the degradation of the Axin protein, weakening β-catenin signaling activation. We confirmed that Ser168 is phosphorylated and that phosphorylation increases Hwa activity in β-catenin signaling and axis induction. Several kinases including Cdk16, Cdk2, and GSK3β, were found to enhance Ser168 phosphorylation in vitro and in vivo. Both dominant-negative Cdk16 expression and pHwa (Ser168) antibody treatment reduce Hwa function. Lastly, a knock-in allele mutating Ser168 to alanine resulted in embryos lacking body axes, demonstrating that Ser168 is essential to axis formation. In summary, Ser168 acts as a phosphorylation switch in Hwa/β-catenin signaling for embryonic axis induction, regulated by multiple kinases.
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publishDate 2024-11-01
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series Nature Communications
spelling doaj-art-9e70f305737b42c49f08a1ae78992a8e2024-11-24T12:33:42ZengNature PortfolioNature Communications2041-17232024-11-0115111510.1038/s41467-024-54450-4A Huluwa phosphorylation switch regulates embryonic axis inductionYao Li0Yun Yan1Bo Gong2Qianwen Zheng3Haiyan Zhou4Jiarui Sun5Mingpeng Li6Zhao Wang7Yaohui Li8Yunjing Wan9Weixi Chen10Shiqian Qi11Xianming Mo12Anming Meng13Bo Xiang14Jing Chen15Department of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Cell and Developmental Biology, Weill Cornell Medicine, Cornell UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Urology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan UniversityLaboratory of Molecular Developmental Biology, State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityDepartment of Pediatric Surgery and Laboratory of Pediatric Surgery, West China Hospital, Sichuan UniversityAbstract Embryonic axis formation is essential for patterning and morphogenesis in vertebrates and is tightly regulated by the dorsal organizer. Previously, we demonstrated that maternally derived Huluwa (Hwa) acts as a dorsal determinant, dictating axis formation by activating β-catenin signaling in zebrafish and Xenopus. However, the mechanism of activation and fine regulation of the Hwa protein remains unclear. Through candidate screening we identified a mutation at Ser168 in the PPNSP motif of Hwa that dramatically abolishes its axis-inducing activity. Mechanistically, mutating the Ser168 residue reduced its binding affinity to Tankyrase 1/2 and the degradation of the Axin protein, weakening β-catenin signaling activation. We confirmed that Ser168 is phosphorylated and that phosphorylation increases Hwa activity in β-catenin signaling and axis induction. Several kinases including Cdk16, Cdk2, and GSK3β, were found to enhance Ser168 phosphorylation in vitro and in vivo. Both dominant-negative Cdk16 expression and pHwa (Ser168) antibody treatment reduce Hwa function. Lastly, a knock-in allele mutating Ser168 to alanine resulted in embryos lacking body axes, demonstrating that Ser168 is essential to axis formation. In summary, Ser168 acts as a phosphorylation switch in Hwa/β-catenin signaling for embryonic axis induction, regulated by multiple kinases.https://doi.org/10.1038/s41467-024-54450-4
spellingShingle Yao Li
Yun Yan
Bo Gong
Qianwen Zheng
Haiyan Zhou
Jiarui Sun
Mingpeng Li
Zhao Wang
Yaohui Li
Yunjing Wan
Weixi Chen
Shiqian Qi
Xianming Mo
Anming Meng
Bo Xiang
Jing Chen
A Huluwa phosphorylation switch regulates embryonic axis induction
Nature Communications
title A Huluwa phosphorylation switch regulates embryonic axis induction
title_full A Huluwa phosphorylation switch regulates embryonic axis induction
title_fullStr A Huluwa phosphorylation switch regulates embryonic axis induction
title_full_unstemmed A Huluwa phosphorylation switch regulates embryonic axis induction
title_short A Huluwa phosphorylation switch regulates embryonic axis induction
title_sort huluwa phosphorylation switch regulates embryonic axis induction
url https://doi.org/10.1038/s41467-024-54450-4
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