YAP/TAZ initiate and maintain schwann cell myelination
dc.creator | Grove, M | |
dc.creator | Kim, H | |
dc.creator | Santerre, M | |
dc.creator | Krupka, AJ | |
dc.creator | Han, SB | |
dc.creator | Zhai, J | |
dc.creator | Cho, JY | |
dc.creator | Park, R | |
dc.creator | Harris, M | |
dc.creator | Kim, S | |
dc.creator | Sawaya, BE | |
dc.creator | Kang, SH | |
dc.creator | Barbe, MF | |
dc.creator | Cho, SH | |
dc.creator | Lemay, MA | |
dc.creator | Son, YJ | |
dc.date.accessioned | 2021-01-25T15:13:54Z | |
dc.date.available | 2021-01-25T15:13:54Z | |
dc.date.issued | 2017-01-26 | |
dc.identifier.issn | 2050-084X | |
dc.identifier.issn | 2050-084X | |
dc.identifier.doi | http://dx.doi.org/10.34944/dspace/4941 | |
dc.identifier.other | 28124973 (pubmed) | |
dc.identifier.uri | http://hdl.handle.net/20.500.12613/4959 | |
dc.description.abstract | © 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. | |
dc.format.extent | e20982- | |
dc.language.iso | en | |
dc.relation.haspart | eLife | |
dc.relation.isreferencedby | eLife Sciences Publications, Ltd | |
dc.rights | CC BY | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Egr2 | |
dc.subject | Schwann cells | |
dc.subject | TEAD | |
dc.subject | Taz | |
dc.subject | demyelination | |
dc.subject | mouse | |
dc.subject | neuroscience | |
dc.subject | Adaptor Proteins, Signal Transducing | |
dc.subject | Animals | |
dc.subject | Cell Cycle Proteins | |
dc.subject | Cell Differentiation | |
dc.subject | Cell Proliferation | |
dc.subject | Mice | |
dc.subject | Myelin Sheath | |
dc.subject | Phosphoproteins | |
dc.subject | Schwann Cells | |
dc.subject | Transcription Factors | |
dc.title | YAP/TAZ initiate and maintain schwann cell myelination | |
dc.type | Article | |
dc.type.genre | Journal Article | |
dc.relation.doi | 10.7554/eLife.20982 | |
dc.ada.note | For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu | |
dc.creator.orcid | Lemay, Michel|0000-0002-5636-0297 | |
dc.date.updated | 2021-01-25T15:13:48Z | |
refterms.dateFOA | 2021-01-25T15:13:54Z |