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  Insm1 Induces Neural Progenitor Delamination in Developing Neocortex via Downregulation of the Adherens Junction Belt-Specific Protein Plekha7

Tavano, S., Taverna, E., Kalebic, N., Haffner, C., Namba, T., Dahl, A., et al. (2018). Insm1 Induces Neural Progenitor Delamination in Developing Neocortex via Downregulation of the Adherens Junction Belt-Specific Protein Plekha7. Neuron, 97(6): e8, pp. 1299-1314. doi:10.1016/j.neuron.2018.01.052.

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 Creators:
Tavano, Stefania, Author
Taverna, Elena1, Author                 
Kalebic, Nereo, Author
Haffner, Christiane, Author
Namba, Takashi, Author
Dahl, Andreas, Author
Wilsch-Bräuninger, Michaela, Author
Paridaen, Judith T. M. L., Author
Huttner, Wieland B., Author
Affiliations:
1Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Max Planck Society, ou_1497672              

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Free keywords: AJ belt disassembly, basal progenitors, basal radial glia, Insm1, NPC delamination, Plekha7, subventricular zone
 Abstract: Summary
Delamination of neural progenitor cells (NPCs) from the ventricular surface is a crucial prerequisite to form the subventricular zone, the germinal layer linked to the expansion of the mammalian neocortex in development and evolution. Here, we dissect the molecular mechanism by which the transcription factor Insm1 promotes the generation of basal progenitors (BPs). Insm1 protein is most highly expressed in newborn BPs in mouse and human developing neocortex. Forced Insm1 expression in embryonic mouse neocortex causes NPC delamination, converting apical to basal radial glia. Insm1 represses the expression of the apical adherens junction belt-specific protein Plekha7. CRISPR/Cas9-mediated disruption of Plekha7 expression suffices to cause NPC delamination. Plekha7 overexpression impedes the intrinsic and counteracts the Insm1-induced, NPC delamination. Our findings uncover a novel molecular mechanism underlying NPC delamination in which a BP-genic transcription factor specifically targets the integrity of the apical adherens junction belt, rather than adherens junction components as such.

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Language(s): eng - English
 Dates: 2018-03-012018-03-21
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.neuron.2018.01.052
 Degree: -

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Title: Neuron
  Alternative Title : Neuron
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: New York : Elsevier
Pages: - Volume / Issue: 97 (6) Sequence Number: e8 Start / End Page: 1299 - 1314 Identifier: ISSN: 0896-6273