A reciprocal regulatory loop between TAZ/YAP and G-protein Gαs regulates Schwann cell proliferation and myelination

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作者
Yaqi Deng
Lai Man Natalie Wu
Shujun Bai
Chuntao Zhao
Haibo Wang
Jincheng Wang
Lingli Xu
Masahide Sakabe
Wenhao Zhou
Mei Xin
Q. Richard Lu
机构
[1] Cincinnati Children’s Hospital Medical Center,Division of Experimental Hematology and Cancer Biology
[2] Key Laboratory of Birth Defects and Related Diseases of Women and Children (Ministry of Education),undefined
[3] State Key Laboratory of Biotherapy,undefined
[4] West China Second Hospital,undefined
[5] Sichuan University,undefined
[6] Institute of Pharmacology and Toxicology,undefined
[7] College of Pharmaceutical Sciences,undefined
[8] Zhejiang University,undefined
[9] Key Laboratory of Birth Defects,undefined
[10] Children’s Hospital of Fudan University,undefined
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Schwann cell (SC) myelination in the peripheral nervous system is essential for motor function, and uncontrolled SC proliferation occurs in cancer. Here, we show that a dual role for Hippo effectors TAZ and YAP in SC proliferation and myelination through modulating G-protein expression and interacting with SOX10, respectively. Developmentally regulated mutagenesis indicates that TAZ/YAP are critical for SC proliferation and differentiation in a stage-dependent manner. Genome-wide occupancy mapping and transcriptome profiling reveal that nuclear TAZ/YAP promote SC proliferation by activating cell cycle regulators, while targeting critical differentiation regulators in cooperation with SOX10 for myelination. We further identify that TAZ targets and represses Gnas, encoding Gαs-protein, which opposes TAZ/YAP activities to decelerate proliferation. Gnas deletion expands SC precursor pools and blocks peripheral myelination. Thus, the Hippo/TAZ/YAP and Gαs-protein feedback circuit functions as a fulcrum balancing SC proliferation and differentiation, providing insights into molecular programming of SC lineage progression and homeostasis.
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