A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development
During the development of the cerebral cortex, neurons are generated directly from radial glial cells or indirectly via basal progenitors. The balance between these division modes determines the number and types of neurons formed in the cortex thereby affecting cortical functioning. Here, we investi...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2020-08-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/58162 |
id |
doaj-4ec1b1854e624433b874c7c5f09a5255 |
---|---|
record_format |
Article |
spelling |
doaj-4ec1b1854e624433b874c7c5f09a52552021-05-05T21:26:29ZengeLife Sciences Publications LtdeLife2050-084X2020-08-01910.7554/eLife.58162A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical developmentKerstin Hasenpusch-Theil0Christine Laclef1Matt Colligan2https://orcid.org/0000-0002-6553-8915Eamon Fitzgerald3Katherine Howe4Emily Carroll5Shaun R Abrams6Jeremy F Reiter7Sylvie Schneider-Maunoury8Thomas Theil9https://orcid.org/0000-0001-6590-8309Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United KingdomSorbonne Université, CNRS UMR7622, INSERM U1156, Institut de Biologie Paris Seine (IBPS) - Developmental Biology Unit, Paris, FranceCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United KingdomCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United KingdomCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United KingdomCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United KingdomDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United StatesDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United States; Chan Zuckerberg Biohub, San Francisco, United StatesSorbonne Université, CNRS UMR7622, INSERM U1156, Institut de Biologie Paris Seine (IBPS) - Developmental Biology Unit, Paris, FranceCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United KingdomDuring the development of the cerebral cortex, neurons are generated directly from radial glial cells or indirectly via basal progenitors. The balance between these division modes determines the number and types of neurons formed in the cortex thereby affecting cortical functioning. Here, we investigate the role of primary cilia in controlling the decision between forming neurons directly or indirectly. We show that a mutation in the ciliary gene Inpp5e leads to a transient increase in direct neurogenesis and subsequently to an overproduction of layer V neurons in newborn mice. Loss of Inpp5e also affects ciliary structure coinciding with reduced Gli3 repressor levels. Genetically restoring Gli3 repressor rescues the decreased indirect neurogenesis in Inpp5e mutants. Overall, our analyses reveal how primary cilia determine neuronal subtype composition of the cortex by controlling direct versus indirect neurogenesis. These findings have implications for understanding cortical malformations in ciliopathies with INPP5E mutations.https://elifesciences.org/articles/58162Inpp5eGli3primary ciliumneurogenesiscortex |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kerstin Hasenpusch-Theil Christine Laclef Matt Colligan Eamon Fitzgerald Katherine Howe Emily Carroll Shaun R Abrams Jeremy F Reiter Sylvie Schneider-Maunoury Thomas Theil |
spellingShingle |
Kerstin Hasenpusch-Theil Christine Laclef Matt Colligan Eamon Fitzgerald Katherine Howe Emily Carroll Shaun R Abrams Jeremy F Reiter Sylvie Schneider-Maunoury Thomas Theil A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development eLife Inpp5e Gli3 primary cilium neurogenesis cortex |
author_facet |
Kerstin Hasenpusch-Theil Christine Laclef Matt Colligan Eamon Fitzgerald Katherine Howe Emily Carroll Shaun R Abrams Jeremy F Reiter Sylvie Schneider-Maunoury Thomas Theil |
author_sort |
Kerstin Hasenpusch-Theil |
title |
A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development |
title_short |
A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development |
title_full |
A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development |
title_fullStr |
A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development |
title_full_unstemmed |
A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development |
title_sort |
transient role of the ciliary gene inpp5e in controlling direct versus indirect neurogenesis in cortical development |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2020-08-01 |
description |
During the development of the cerebral cortex, neurons are generated directly from radial glial cells or indirectly via basal progenitors. The balance between these division modes determines the number and types of neurons formed in the cortex thereby affecting cortical functioning. Here, we investigate the role of primary cilia in controlling the decision between forming neurons directly or indirectly. We show that a mutation in the ciliary gene Inpp5e leads to a transient increase in direct neurogenesis and subsequently to an overproduction of layer V neurons in newborn mice. Loss of Inpp5e also affects ciliary structure coinciding with reduced Gli3 repressor levels. Genetically restoring Gli3 repressor rescues the decreased indirect neurogenesis in Inpp5e mutants. Overall, our analyses reveal how primary cilia determine neuronal subtype composition of the cortex by controlling direct versus indirect neurogenesis. These findings have implications for understanding cortical malformations in ciliopathies with INPP5E mutations. |
topic |
Inpp5e Gli3 primary cilium neurogenesis cortex |
url |
https://elifesciences.org/articles/58162 |
work_keys_str_mv |
AT kerstinhasenpuschtheil atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT christinelaclef atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT mattcolligan atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT eamonfitzgerald atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT katherinehowe atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT emilycarroll atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT shaunrabrams atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT jeremyfreiter atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT sylvieschneidermaunoury atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT thomastheil atransientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT kerstinhasenpuschtheil transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT christinelaclef transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT mattcolligan transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT eamonfitzgerald transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT katherinehowe transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT emilycarroll transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT shaunrabrams transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT jeremyfreiter transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT sylvieschneidermaunoury transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment AT thomastheil transientroleoftheciliarygeneinpp5eincontrollingdirectversusindirectneurogenesisincorticaldevelopment |
_version_ |
1721458113195802624 |