Cargando…
miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition
During neurogenesis, generation, migration and integration of the correct numbers of each neuron sub-type depends on complex molecular interactions in space and time. MicroRNAs represent a key control level allowing the flexibility and stability needed for this process. Insight into the role of this...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073329/ https://www.ncbi.nlm.nih.gov/pubmed/27767083 http://dx.doi.org/10.1038/srep35729 |
_version_ | 1782461552597663744 |
---|---|
author | Beclin, Christophe Follert, Philipp Stappers, Elke Barral, Serena Nathalie, Coré de Chevigny, Antoine Magnone, Virginie Lebrigand, Kévin Bissels, Ute Huylebroeck, Danny Bosio, Andreas Barbry, Pascal Seuntjens, Eve Cremer, Harold |
author_facet | Beclin, Christophe Follert, Philipp Stappers, Elke Barral, Serena Nathalie, Coré de Chevigny, Antoine Magnone, Virginie Lebrigand, Kévin Bissels, Ute Huylebroeck, Danny Bosio, Andreas Barbry, Pascal Seuntjens, Eve Cremer, Harold |
author_sort | Beclin, Christophe |
collection | PubMed |
description | During neurogenesis, generation, migration and integration of the correct numbers of each neuron sub-type depends on complex molecular interactions in space and time. MicroRNAs represent a key control level allowing the flexibility and stability needed for this process. Insight into the role of this regulatory pathway in the brain is still limited. We performed a sequential experimental approach using postnatal olfactory bulb neurogenesis in mice, starting from global expression analyses to the investigation of functional interactions between defined microRNAs and their targets. Deep sequencing of small RNAs extracted from defined compartments of the postnatal neurogenic system demonstrated that the miR-200 family is specifically induced during late neuronal differentiation stages. Using in vivo strategies we interfered with the entire miR-200 family in loss- and gain-of-function settings, showing a role of miR-200 in neuronal maturation. This function is mediated by targeting the transcription factor Zeb2. Interestingly, so far functional interaction between miR-200 and Zeb2 has been exclusively reported in cancer or cultured stem cells. Our data demonstrate that this regulatory interaction is also active during normal neurogenesis. |
format | Online Article Text |
id | pubmed-5073329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50733292016-10-26 miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition Beclin, Christophe Follert, Philipp Stappers, Elke Barral, Serena Nathalie, Coré de Chevigny, Antoine Magnone, Virginie Lebrigand, Kévin Bissels, Ute Huylebroeck, Danny Bosio, Andreas Barbry, Pascal Seuntjens, Eve Cremer, Harold Sci Rep Article During neurogenesis, generation, migration and integration of the correct numbers of each neuron sub-type depends on complex molecular interactions in space and time. MicroRNAs represent a key control level allowing the flexibility and stability needed for this process. Insight into the role of this regulatory pathway in the brain is still limited. We performed a sequential experimental approach using postnatal olfactory bulb neurogenesis in mice, starting from global expression analyses to the investigation of functional interactions between defined microRNAs and their targets. Deep sequencing of small RNAs extracted from defined compartments of the postnatal neurogenic system demonstrated that the miR-200 family is specifically induced during late neuronal differentiation stages. Using in vivo strategies we interfered with the entire miR-200 family in loss- and gain-of-function settings, showing a role of miR-200 in neuronal maturation. This function is mediated by targeting the transcription factor Zeb2. Interestingly, so far functional interaction between miR-200 and Zeb2 has been exclusively reported in cancer or cultured stem cells. Our data demonstrate that this regulatory interaction is also active during normal neurogenesis. Nature Publishing Group 2016-10-21 /pmc/articles/PMC5073329/ /pubmed/27767083 http://dx.doi.org/10.1038/srep35729 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Beclin, Christophe Follert, Philipp Stappers, Elke Barral, Serena Nathalie, Coré de Chevigny, Antoine Magnone, Virginie Lebrigand, Kévin Bissels, Ute Huylebroeck, Danny Bosio, Andreas Barbry, Pascal Seuntjens, Eve Cremer, Harold miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title | miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title_full | miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title_fullStr | miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title_full_unstemmed | miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title_short | miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition |
title_sort | mir-200 family controls late steps of postnatal forebrain neurogenesis via zeb2 inhibition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073329/ https://www.ncbi.nlm.nih.gov/pubmed/27767083 http://dx.doi.org/10.1038/srep35729 |
work_keys_str_mv | AT beclinchristophe mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT follertphilipp mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT stapperselke mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT barralserena mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT nathaliecore mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT dechevignyantoine mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT magnonevirginie mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT lebrigandkevin mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT bisselsute mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT huylebroeckdanny mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT bosioandreas mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT barbrypascal mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT seuntjenseve mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition AT cremerharold mir200familycontrolslatestepsofpostnatalforebrainneurogenesisviazeb2inhibition |