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Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq

In jawed vertebrates, oligodendrocytes (OLs) are the myelin-producing glial cells responsible for ensheathment of axons within the central nervous system and are also crucial for remyelination following injury or disease. Olig2 is a crucial factor in the specification and differentiation of oligoden...

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Autores principales: Darr, Andrew J., Danzi, Matt C., Brady, Lee, Emig-Agius, Dorothea, Hackett, Amber, Golshani, Roozbeh, Warner, Nikita, Lee, Jae, Lemmon, Vance P., Tsoulfas, Pantelis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648140/
https://www.ncbi.nlm.nih.gov/pubmed/29049317
http://dx.doi.org/10.1371/journal.pone.0186091
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author Darr, Andrew J.
Danzi, Matt C.
Brady, Lee
Emig-Agius, Dorothea
Hackett, Amber
Golshani, Roozbeh
Warner, Nikita
Lee, Jae
Lemmon, Vance P.
Tsoulfas, Pantelis
author_facet Darr, Andrew J.
Danzi, Matt C.
Brady, Lee
Emig-Agius, Dorothea
Hackett, Amber
Golshani, Roozbeh
Warner, Nikita
Lee, Jae
Lemmon, Vance P.
Tsoulfas, Pantelis
author_sort Darr, Andrew J.
collection PubMed
description In jawed vertebrates, oligodendrocytes (OLs) are the myelin-producing glial cells responsible for ensheathment of axons within the central nervous system and are also crucial for remyelination following injury or disease. Olig2 is a crucial factor in the specification and differentiation of oligodendrocyte precursor cells (OPCs) that give rise to mature, myelin-producing OLs in the developing and postnatal CNS; however, its role in adulthood is less well understood. To investigate the role Olig2 plays in regulating gene expression in the adult OL lineage in a physiologically-relevant context, we performed chromatin immunoprecipitation followed by next generation sequencing analysis (ChIP-Seq) using whole spinal cord tissue harvested from adult mice. We found that many of the Olig2-bound sites were associated with genes with biological processes corresponding to OL differentiation (Nkx2.2, Nkx6.2, and Sip1), myelination and ensheathment (Mbp, Cldn11, and Mobp), as well as cell cycle and cytoskeletal regulation. This suggests Olig2 continues to play a critical role in processes related to OL differentiation and myelination well into adulthood.
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spelling pubmed-56481402017-11-03 Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq Darr, Andrew J. Danzi, Matt C. Brady, Lee Emig-Agius, Dorothea Hackett, Amber Golshani, Roozbeh Warner, Nikita Lee, Jae Lemmon, Vance P. Tsoulfas, Pantelis PLoS One Research Article In jawed vertebrates, oligodendrocytes (OLs) are the myelin-producing glial cells responsible for ensheathment of axons within the central nervous system and are also crucial for remyelination following injury or disease. Olig2 is a crucial factor in the specification and differentiation of oligodendrocyte precursor cells (OPCs) that give rise to mature, myelin-producing OLs in the developing and postnatal CNS; however, its role in adulthood is less well understood. To investigate the role Olig2 plays in regulating gene expression in the adult OL lineage in a physiologically-relevant context, we performed chromatin immunoprecipitation followed by next generation sequencing analysis (ChIP-Seq) using whole spinal cord tissue harvested from adult mice. We found that many of the Olig2-bound sites were associated with genes with biological processes corresponding to OL differentiation (Nkx2.2, Nkx6.2, and Sip1), myelination and ensheathment (Mbp, Cldn11, and Mobp), as well as cell cycle and cytoskeletal regulation. This suggests Olig2 continues to play a critical role in processes related to OL differentiation and myelination well into adulthood. Public Library of Science 2017-10-19 /pmc/articles/PMC5648140/ /pubmed/29049317 http://dx.doi.org/10.1371/journal.pone.0186091 Text en © 2017 Darr et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Darr, Andrew J.
Danzi, Matt C.
Brady, Lee
Emig-Agius, Dorothea
Hackett, Amber
Golshani, Roozbeh
Warner, Nikita
Lee, Jae
Lemmon, Vance P.
Tsoulfas, Pantelis
Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title_full Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title_fullStr Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title_full_unstemmed Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title_short Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
title_sort identification of genome-wide targets of olig2 in the adult mouse spinal cord using chip-seq
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648140/
https://www.ncbi.nlm.nih.gov/pubmed/29049317
http://dx.doi.org/10.1371/journal.pone.0186091
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