Genre
Journal ArticleDate
2017-01-26Author
Grove, MKim, H
Santerre, M
Krupka, AJ
Han, SB
Zhai, J
Cho, JY
Park, R
Harris, M
Kim, S
Sawaya, BE
Kang, SH
Barbe, MF
Cho, SH
Lemay, MA
Son, YJ
Subject
Egr2Schwann cells
TEAD
Taz
demyelination
mouse
neuroscience
Adaptor Proteins, Signal Transducing
Animals
Cell Cycle Proteins
Cell Differentiation
Cell Proliferation
Mice
Myelin Sheath
Phosphoproteins
Schwann Cells
Transcription Factors
Permanent link to this record
http://hdl.handle.net/20.500.12613/4959
Metadata
Show full item recordDOI
10.7554/eLife.20982Abstract
© Grove et al. 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.Citation to related work
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http://dx.doi.org/10.34944/dspace/4941