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Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum

To identify chromatin mechanisms of neuronal differentiation, we characterized chromatin accessibility and gene expression in cerebellar granule neurons (CGNs) of the developing mouse. We used DNase-seq to map accessibility of cis-regulatory elements and RNA-seq to profile transcript abundance acros...

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Autores principales: Frank, Christopher L., Liu, Fang, Wijayatunge, Ranjula, Song, Lingyun, Biegler, Matthew T., Yang, Marty G., Vockley, Christopher M., Safi, Alexias, Gersbach, Charles A., Crawford, Gregory E., West, Anne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414887/
https://www.ncbi.nlm.nih.gov/pubmed/25849986
http://dx.doi.org/10.1038/nn.3995
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author Frank, Christopher L.
Liu, Fang
Wijayatunge, Ranjula
Song, Lingyun
Biegler, Matthew T.
Yang, Marty G.
Vockley, Christopher M.
Safi, Alexias
Gersbach, Charles A.
Crawford, Gregory E.
West, Anne E.
author_facet Frank, Christopher L.
Liu, Fang
Wijayatunge, Ranjula
Song, Lingyun
Biegler, Matthew T.
Yang, Marty G.
Vockley, Christopher M.
Safi, Alexias
Gersbach, Charles A.
Crawford, Gregory E.
West, Anne E.
author_sort Frank, Christopher L.
collection PubMed
description To identify chromatin mechanisms of neuronal differentiation, we characterized chromatin accessibility and gene expression in cerebellar granule neurons (CGNs) of the developing mouse. We used DNase-seq to map accessibility of cis-regulatory elements and RNA-seq to profile transcript abundance across postnatal stages of neuronal differentiation in vivo and in culture. We observed thousands of chromatin accessibility changes as CGNs differentiated and verified by H3K27ac ChIP-seq, reporter gene assays, and CRISPR-mediated activation that many of these regions function as neuronal enhancers. Motif discovery within differentially accessible chromatin regions suggested a novel role for the Zic family of transcription factors in CGN maturation. We confirmed the association of Zic with these elements by ChIP-seq, and demonstrated by knockdown that Zic1/2 are required to coordinate mature neuronal gene expression patterns. Together these data reveal chromatin dynamics at thousands of gene regulatory elements that facilitate gene expression patterns necessary for neuronal differentiation and function.
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spelling pubmed-44148872015-11-01 Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum Frank, Christopher L. Liu, Fang Wijayatunge, Ranjula Song, Lingyun Biegler, Matthew T. Yang, Marty G. Vockley, Christopher M. Safi, Alexias Gersbach, Charles A. Crawford, Gregory E. West, Anne E. Nat Neurosci Article To identify chromatin mechanisms of neuronal differentiation, we characterized chromatin accessibility and gene expression in cerebellar granule neurons (CGNs) of the developing mouse. We used DNase-seq to map accessibility of cis-regulatory elements and RNA-seq to profile transcript abundance across postnatal stages of neuronal differentiation in vivo and in culture. We observed thousands of chromatin accessibility changes as CGNs differentiated and verified by H3K27ac ChIP-seq, reporter gene assays, and CRISPR-mediated activation that many of these regions function as neuronal enhancers. Motif discovery within differentially accessible chromatin regions suggested a novel role for the Zic family of transcription factors in CGN maturation. We confirmed the association of Zic with these elements by ChIP-seq, and demonstrated by knockdown that Zic1/2 are required to coordinate mature neuronal gene expression patterns. Together these data reveal chromatin dynamics at thousands of gene regulatory elements that facilitate gene expression patterns necessary for neuronal differentiation and function. 2015-04-06 2015-05 /pmc/articles/PMC4414887/ /pubmed/25849986 http://dx.doi.org/10.1038/nn.3995 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Frank, Christopher L.
Liu, Fang
Wijayatunge, Ranjula
Song, Lingyun
Biegler, Matthew T.
Yang, Marty G.
Vockley, Christopher M.
Safi, Alexias
Gersbach, Charles A.
Crawford, Gregory E.
West, Anne E.
Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title_full Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title_fullStr Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title_full_unstemmed Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title_short Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum
title_sort regulation of chromatin accessibility and zic binding at enhancers in the developing cerebellum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414887/
https://www.ncbi.nlm.nih.gov/pubmed/25849986
http://dx.doi.org/10.1038/nn.3995
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