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RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors
In developing brain neuronal migration, dendrite outgrowth and dendritic spine outgrowth are controlled by Cdc42, a small GTPase of the Rho family, and its activators. Cdc42 function in promoting actin polymerization is crucial for glutamatergic synapse regulation. Here, we focus on GABAergic synaps...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673238/ https://www.ncbi.nlm.nih.gov/pubmed/29069083 http://dx.doi.org/10.1371/journal.pgen.1007073 |
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author | de Groot, Claire Floriou-Servou, Amalia Tsai, Yuan-Chen Früh, Simon Kohler, Manuela Parkin, Georgia Schwerdel, Cornelia Bosshard, Giovanna Kaila, Kai Fritschy, Jean-Marc Tyagarajan, Shiva K. |
author_facet | de Groot, Claire Floriou-Servou, Amalia Tsai, Yuan-Chen Früh, Simon Kohler, Manuela Parkin, Georgia Schwerdel, Cornelia Bosshard, Giovanna Kaila, Kai Fritschy, Jean-Marc Tyagarajan, Shiva K. |
author_sort | de Groot, Claire |
collection | PubMed |
description | In developing brain neuronal migration, dendrite outgrowth and dendritic spine outgrowth are controlled by Cdc42, a small GTPase of the Rho family, and its activators. Cdc42 function in promoting actin polymerization is crucial for glutamatergic synapse regulation. Here, we focus on GABAergic synapse-specific activator of Cdc42, collybistin (CB) and examine functional differences between its splice isoforms CB1 and CB2. We report that CB1 and CB2 differentially regulate GABAergic synapse formation in vitro along proximal-distal axis and adult-born neuron maturation in vivo. The functional specialization between CB1 and CB2 isoforms arises from their differential protein half-life, in turn regulated by ubiquitin conjugation of the unique CB1 C-terminus. We report that CB1 and CB2 negatively regulate Cdc42; however, Cdc42 activation is dependent on CB interaction with gephyrin. During hippocampal adult neurogenesis CB1 regulates neuronal migration, while CB2 is essential for dendrite outgrowth. Finally, using mice lacking Gabra2 subunit, we show that CB1 function is downstream of GABA(A)Rs, and we can rescue adult neurogenesis deficit observed in Gabra2 KO. Overall, our results uncover previously unexpected role for CB isoforms downstream of α2-containing GABA(A)Rs during neuron maturation in a Cdc42 dependent mechanism. |
format | Online Article Text |
id | pubmed-5673238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56732382017-11-18 RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors de Groot, Claire Floriou-Servou, Amalia Tsai, Yuan-Chen Früh, Simon Kohler, Manuela Parkin, Georgia Schwerdel, Cornelia Bosshard, Giovanna Kaila, Kai Fritschy, Jean-Marc Tyagarajan, Shiva K. PLoS Genet Research Article In developing brain neuronal migration, dendrite outgrowth and dendritic spine outgrowth are controlled by Cdc42, a small GTPase of the Rho family, and its activators. Cdc42 function in promoting actin polymerization is crucial for glutamatergic synapse regulation. Here, we focus on GABAergic synapse-specific activator of Cdc42, collybistin (CB) and examine functional differences between its splice isoforms CB1 and CB2. We report that CB1 and CB2 differentially regulate GABAergic synapse formation in vitro along proximal-distal axis and adult-born neuron maturation in vivo. The functional specialization between CB1 and CB2 isoforms arises from their differential protein half-life, in turn regulated by ubiquitin conjugation of the unique CB1 C-terminus. We report that CB1 and CB2 negatively regulate Cdc42; however, Cdc42 activation is dependent on CB interaction with gephyrin. During hippocampal adult neurogenesis CB1 regulates neuronal migration, while CB2 is essential for dendrite outgrowth. Finally, using mice lacking Gabra2 subunit, we show that CB1 function is downstream of GABA(A)Rs, and we can rescue adult neurogenesis deficit observed in Gabra2 KO. Overall, our results uncover previously unexpected role for CB isoforms downstream of α2-containing GABA(A)Rs during neuron maturation in a Cdc42 dependent mechanism. Public Library of Science 2017-10-25 /pmc/articles/PMC5673238/ /pubmed/29069083 http://dx.doi.org/10.1371/journal.pgen.1007073 Text en © 2017 de Groot et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article de Groot, Claire Floriou-Servou, Amalia Tsai, Yuan-Chen Früh, Simon Kohler, Manuela Parkin, Georgia Schwerdel, Cornelia Bosshard, Giovanna Kaila, Kai Fritschy, Jean-Marc Tyagarajan, Shiva K. RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title | RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title_full | RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title_fullStr | RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title_full_unstemmed | RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title_short | RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABA(A) receptors |
title_sort | rhogef9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 gaba(a) receptors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673238/ https://www.ncbi.nlm.nih.gov/pubmed/29069083 http://dx.doi.org/10.1371/journal.pgen.1007073 |
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