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Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence

The majority of neural stem cells (NSCs) in the adult brain are quiescent, and this fraction increases with aging. Although signaling pathways that promote NSC quiescence have been identified, the transcriptional mechanisms involved are mostly unknown, largely due to lack of a cell culture model. In...

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Autores principales: Martynoga, Ben, Mateo, Juan L., Zhou, Bo, Andersen, Jimena, Achimastou, Angeliki, Urbán, Noelia, van den Berg, Debbie, Georgopoulou, Dimitra, Hadjur, Suzana, Wittbrodt, Joachim, Ettwiller, Laurence, Piper, Michael, Gronostajski, Richard M., Guillemot, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759694/
https://www.ncbi.nlm.nih.gov/pubmed/23964093
http://dx.doi.org/10.1101/gad.216804.113
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author Martynoga, Ben
Mateo, Juan L.
Zhou, Bo
Andersen, Jimena
Achimastou, Angeliki
Urbán, Noelia
van den Berg, Debbie
Georgopoulou, Dimitra
Hadjur, Suzana
Wittbrodt, Joachim
Ettwiller, Laurence
Piper, Michael
Gronostajski, Richard M.
Guillemot, François
author_facet Martynoga, Ben
Mateo, Juan L.
Zhou, Bo
Andersen, Jimena
Achimastou, Angeliki
Urbán, Noelia
van den Berg, Debbie
Georgopoulou, Dimitra
Hadjur, Suzana
Wittbrodt, Joachim
Ettwiller, Laurence
Piper, Michael
Gronostajski, Richard M.
Guillemot, François
author_sort Martynoga, Ben
collection PubMed
description The majority of neural stem cells (NSCs) in the adult brain are quiescent, and this fraction increases with aging. Although signaling pathways that promote NSC quiescence have been identified, the transcriptional mechanisms involved are mostly unknown, largely due to lack of a cell culture model. In this study, we first demonstrate that NSC cultures (NS cells) exposed to BMP4 acquire cellular and transcriptional characteristics of quiescent cells. We then use epigenomic profiling to identify enhancers associated with the quiescent NS cell state. Motif enrichment analysis of these enhancers predicts a major role for the nuclear factor one (NFI) family in the gene regulatory network controlling NS cell quiescence. Interestingly, we found that the family member NFIX is robustly induced when NS cells enter quiescence. Using genome-wide location analysis and overexpression and silencing experiments, we demonstrate that NFIX has a major role in the induction of quiescence in cultured NSCs. Transcript profiling of NS cells overexpressing or silenced for Nfix and the phenotypic analysis of the hippocampus of Nfix mutant mice suggest that NFIX controls the quiescent state by regulating the interactions of NSCs with their microenvironment.
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spelling pubmed-37596942013-09-04 Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence Martynoga, Ben Mateo, Juan L. Zhou, Bo Andersen, Jimena Achimastou, Angeliki Urbán, Noelia van den Berg, Debbie Georgopoulou, Dimitra Hadjur, Suzana Wittbrodt, Joachim Ettwiller, Laurence Piper, Michael Gronostajski, Richard M. Guillemot, François Genes Dev Research Paper The majority of neural stem cells (NSCs) in the adult brain are quiescent, and this fraction increases with aging. Although signaling pathways that promote NSC quiescence have been identified, the transcriptional mechanisms involved are mostly unknown, largely due to lack of a cell culture model. In this study, we first demonstrate that NSC cultures (NS cells) exposed to BMP4 acquire cellular and transcriptional characteristics of quiescent cells. We then use epigenomic profiling to identify enhancers associated with the quiescent NS cell state. Motif enrichment analysis of these enhancers predicts a major role for the nuclear factor one (NFI) family in the gene regulatory network controlling NS cell quiescence. Interestingly, we found that the family member NFIX is robustly induced when NS cells enter quiescence. Using genome-wide location analysis and overexpression and silencing experiments, we demonstrate that NFIX has a major role in the induction of quiescence in cultured NSCs. Transcript profiling of NS cells overexpressing or silenced for Nfix and the phenotypic analysis of the hippocampus of Nfix mutant mice suggest that NFIX controls the quiescent state by regulating the interactions of NSCs with their microenvironment. Cold Spring Harbor Laboratory Press 2013-08-15 /pmc/articles/PMC3759694/ /pubmed/23964093 http://dx.doi.org/10.1101/gad.216804.113 Text en © 2013, Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research Paper
Martynoga, Ben
Mateo, Juan L.
Zhou, Bo
Andersen, Jimena
Achimastou, Angeliki
Urbán, Noelia
van den Berg, Debbie
Georgopoulou, Dimitra
Hadjur, Suzana
Wittbrodt, Joachim
Ettwiller, Laurence
Piper, Michael
Gronostajski, Richard M.
Guillemot, François
Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title_full Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title_fullStr Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title_full_unstemmed Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title_short Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence
title_sort epigenomic enhancer annotation reveals a key role for nfix in neural stem cell quiescence
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759694/
https://www.ncbi.nlm.nih.gov/pubmed/23964093
http://dx.doi.org/10.1101/gad.216804.113
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