eLife (Jan 2017)

YAP/TAZ initiate and maintain Schwann cell myelination

  • Matthew Grove,
  • Hyukmin Kim,
  • Maryline Santerre,
  • Alexander J Krupka,
  • Seung Baek Han,
  • Jinbin Zhai,
  • Jennifer Y Cho,
  • Raehee Park,
  • Michele Harris,
  • Seonhee Kim,
  • Bassel E Sawaya,
  • Shin H Kang,
  • Mary F Barbe,
  • Seo-Hee Cho,
  • Michel A Lemay,
  • Young-Jin Son

DOI
https://doi.org/10.7554/eLife.20982
Journal volume & issue
Vol. 6

Abstract

Read online

Nuclear exclusion of the transcriptional regulators and potent oncoproteins, YAP/TAZ, is considered necessary for adult tissue homeostasis. Here we show that nuclear YAP/TAZ are essential regulators of peripheral nerve development and myelin maintenance. To proliferate, developing Schwann cells (SCs) require YAP/TAZ to enter S-phase and, without them, fail to generate sufficient SCs for timely axon sorting. To differentiate, SCs require YAP/TAZ to upregulate Krox20 and, without them, completely fail to myelinate, resulting in severe peripheral neuropathy. Remarkably, in adulthood, nuclear YAP/TAZ are selectively expressed by myelinating SCs, and conditional ablation results in severe peripheral demyelination and mouse death. YAP/TAZ regulate both developmental and adult myelination by driving TEAD1 to activate Krox20. Therefore, YAP/TAZ are crucial for SCs to myelinate developing nerve and to maintain myelinated nerve in adulthood. Our study also provides a new insight into the role of nuclear YAP/TAZ in homeostatic maintenance of an adult tissue.

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