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  Beta phorbol ester- and diacylglycerol-induced augmentation of transmitter release is mediated by Munc13s and not by PKCs

Rhee, J. S., Betz, A., Pyott, S., Reim, K., Varoqueaux, F., Augustin, I., et al. (2002). Beta phorbol ester- and diacylglycerol-induced augmentation of transmitter release is mediated by Munc13s and not by PKCs. Cell, 108(1), 121-133.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0029-0BD6-5 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0029-0BD7-3
Genre: Journal Article

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 Creators:
Rhee, J. S., Author
Betz, Andrea1, Author           
Pyott, S., Author
Reim, Kerstin2, Author           
Varoqueaux, Frédérique2, Author           
Augustin, I., Author
Hesse, D., Author
Südhof, Thomas C., Author
Takahashi, M., Author
Rosenmund, Christian, Author
Brose, Nils2, Author           
Affiliations:
1Max Planck Institute of Experimental Medicine, ou_586201              
2Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173659              

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 Abstract: Munc13-1 is a presynaptic protein with an essential role in synaptic vesicle priming. It contains a diacylglycerol (DAG)/beta phorbol ester binding C-1 domain and is a potential target of the DAG second messenger pathway that may act in parallel with PKCs. Using genetically modified mice that express a DAG/beta phorbol ester binding-deficient Munc13- 1(H567K) variant instead of the wild-type protein, we determined the relative contribution of PKCs and Munc13-1 to DAG/beta phorbol ester-dependent regulation of neurotransmitter release. We show that Munc13s are the main presynaptic DAG/beta phorbol ester receptors in hippocampal neurons. Modulation of Munc13-1 activity by second messengers via the DAG/beta phorbol ester binding C-1 domain is essential for use-dependent alterations of synaptic efficacy and survival.

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Language(s): eng - English
 Dates: 2002-01-11
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 17314
ISI: 000173280700013
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Title: Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 108 (1) Sequence Number: - Start / End Page: 121 - 133 Identifier: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183