Cargando…

Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy

Evidence is lacking as to how developing neurons integrate mitogenic signals with microenvironment cues to control proliferation and differentiation. We determine that the Siah2 E3 ubiquitin ligase functions in a coincidence detection circuit linking responses to the Shh mitogen and the extracellula...

Descripción completa

Detalles Bibliográficos
Autores principales: Ong, Taren, Trivedi, Niraj, Wakefield, Randall, Frase, Sharon, Solecki, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576183/
https://www.ncbi.nlm.nih.gov/pubmed/33082319
http://dx.doi.org/10.1038/s41467-020-19063-7
_version_ 1783597965281067008
author Ong, Taren
Trivedi, Niraj
Wakefield, Randall
Frase, Sharon
Solecki, David J.
author_facet Ong, Taren
Trivedi, Niraj
Wakefield, Randall
Frase, Sharon
Solecki, David J.
author_sort Ong, Taren
collection PubMed
description Evidence is lacking as to how developing neurons integrate mitogenic signals with microenvironment cues to control proliferation and differentiation. We determine that the Siah2 E3 ubiquitin ligase functions in a coincidence detection circuit linking responses to the Shh mitogen and the extracellular matrix to control cerebellar granule neurons (CGN) GZ occupancy. We show that Shh signaling maintains Siah2 expression in CGN progenitors (GNPs) in a Ras/Mapk-dependent manner. Siah2 supports ciliogenesis in a feed-forward fashion by restraining cilium disassembly. Efforts to identify sources of the Ras/Mapk signaling led us to discover that GNPs respond to laminin, but not vitronectin, in the GZ microenvironment via integrin β1 receptors, which engages the Ras/Mapk cascade with Shh, and that this niche interaction is essential for promoting GNP ciliogenesis. As GNPs leave the GZ, differentiation is driven by changing extracellular cues that diminish Siah2-activity leading to primary cilia shortening and attenuation of the mitogenic response.
format Online
Article
Text
id pubmed-7576183
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75761832020-10-29 Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy Ong, Taren Trivedi, Niraj Wakefield, Randall Frase, Sharon Solecki, David J. Nat Commun Article Evidence is lacking as to how developing neurons integrate mitogenic signals with microenvironment cues to control proliferation and differentiation. We determine that the Siah2 E3 ubiquitin ligase functions in a coincidence detection circuit linking responses to the Shh mitogen and the extracellular matrix to control cerebellar granule neurons (CGN) GZ occupancy. We show that Shh signaling maintains Siah2 expression in CGN progenitors (GNPs) in a Ras/Mapk-dependent manner. Siah2 supports ciliogenesis in a feed-forward fashion by restraining cilium disassembly. Efforts to identify sources of the Ras/Mapk signaling led us to discover that GNPs respond to laminin, but not vitronectin, in the GZ microenvironment via integrin β1 receptors, which engages the Ras/Mapk cascade with Shh, and that this niche interaction is essential for promoting GNP ciliogenesis. As GNPs leave the GZ, differentiation is driven by changing extracellular cues that diminish Siah2-activity leading to primary cilia shortening and attenuation of the mitogenic response. Nature Publishing Group UK 2020-10-20 /pmc/articles/PMC7576183/ /pubmed/33082319 http://dx.doi.org/10.1038/s41467-020-19063-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ong, Taren
Trivedi, Niraj
Wakefield, Randall
Frase, Sharon
Solecki, David J.
Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title_full Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title_fullStr Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title_full_unstemmed Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title_short Siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
title_sort siah2 integrates mitogenic and extracellular matrix signals linking neuronal progenitor ciliogenesis with germinal zone occupancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576183/
https://www.ncbi.nlm.nih.gov/pubmed/33082319
http://dx.doi.org/10.1038/s41467-020-19063-7
work_keys_str_mv AT ongtaren siah2integratesmitogenicandextracellularmatrixsignalslinkingneuronalprogenitorciliogenesiswithgerminalzoneoccupancy
AT trivediniraj siah2integratesmitogenicandextracellularmatrixsignalslinkingneuronalprogenitorciliogenesiswithgerminalzoneoccupancy
AT wakefieldrandall siah2integratesmitogenicandextracellularmatrixsignalslinkingneuronalprogenitorciliogenesiswithgerminalzoneoccupancy
AT frasesharon siah2integratesmitogenicandextracellularmatrixsignalslinkingneuronalprogenitorciliogenesiswithgerminalzoneoccupancy
AT soleckidavidj siah2integratesmitogenicandextracellularmatrixsignalslinkingneuronalprogenitorciliogenesiswithgerminalzoneoccupancy