Chromatin Remodeling BAF155 Subunit Regulates the Genesis of Basal Progenitors in Developing Cortex

The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation...

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Published iniScience Vol. 4; pp. 109 - 126
Main Authors Narayanan, Ramanathan, Pham, Linh, Kerimoglu, Cemil, Watanabe, Takashi, Castro Hernandez, Ricardo, Sokpor, Godwin, Ulmke, Pauline Antonie, Kiszka, Kamila A., Tonchev, Anton B., Rosenbusch, Joachim, Seong, Rho H., Teichmann, Ulrike, Frahm, Jens, Fischer, Andre, Bonn, Stefan, Stoykova, Anastassia, Staiger, Jochen F., Tuoc, Tran
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 29.06.2018
Elsevier
Subjects
Developmental Neuroscience
Molecular Neuroscience
Neuroscience
Molecular Neuroscience
Neuroscience
Developmental Neuroscience
Online AccessGet full text
ISSN2589-0042
2589-0042
DOI10.1016/j.isci.2018.05.014

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Abstract The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance. [Display omitted] •BAF155 potentiates PAX6 transcriptional activity•BAF155 and PAX6 co-regulate bIP genesis in developing cerebral cortex•BAF155 and PAX6 control bRG genesis through aRG delamination non-cell-autonomously•BAF155 suppresses the expression of human RG-specific genes in developing mouse cortex Neuroscience; Molecular Neuroscience; Developmental Neuroscience
AbstractList The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance.The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance.
The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance.
The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance. [Display omitted] •BAF155 potentiates PAX6 transcriptional activity•BAF155 and PAX6 co-regulate bIP genesis in developing cerebral cortex•BAF155 and PAX6 control bRG genesis through aRG delamination non-cell-autonomously•BAF155 suppresses the expression of human RG-specific genes in developing mouse cortex Neuroscience; Molecular Neuroscience; Developmental Neuroscience
The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4) that possibly acquired evolutionary significance. : Neuroscience; Molecular Neuroscience; Developmental Neuroscience Subject Areas: Neuroscience, Molecular Neuroscience, Developmental Neuroscience
The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated to the high degree of cortical folding. Here we examined the role of BAF155, a subunit of the chromatin remodeling BAF complex, in generation of cortical progenitor heterogeneity. The conditional deletion of BAF155 led to diminished bIP pool and increased number of bRGs, due to delamination of apical RGs. We found that BAF155 is required for normal activity of neurogenic transcription factor PAX6, thus controlling the expression of genes that are involved in bIP specification, cell-cell interaction, and establishment of adherens junction. In a PAX6-dependent manner, BAF155 regulates the expression of the CDC42 effector protein CEP4, thereby controlling progenitor delamination. Furthermore, BAF155-dependent chromatin remodeling seems to exert a specific role in the genesis of BPs through the regulation of human RG-specific genes (such as Foxn4 ) that possibly acquired evolutionary significance. • BAF155 potentiates PAX6 transcriptional activity • BAF155 and PAX6 co-regulate bIP genesis in developing cerebral cortex • BAF155 and PAX6 control bRG genesis through aRG delamination non-cell-autonomously • BAF155 suppresses the expression of human RG-specific genes in developing mouse cortex Neuroscience; Molecular Neuroscience; Developmental Neuroscience
Author Kerimoglu, Cemil
Castro Hernandez, Ricardo
Fischer, Andre
Frahm, Jens
Tonchev, Anton B.
Kiszka, Kamila A.
Bonn, Stefan
Ulmke, Pauline Antonie
Narayanan, Ramanathan
Staiger, Jochen F.
Stoykova, Anastassia
Seong, Rho H.
Rosenbusch, Joachim
Watanabe, Takashi
Pham, Linh
Teichmann, Ulrike
Sokpor, Godwin
Tuoc, Tran
AuthorAffiliation 4 Department of Biological Sciences, Institute of Molecular Biology and Genetics, Seoul National University, Seoul 08826, Korea
5 DFG, Center for Molecular Physiology of the Brain (CMPB), 37075 Goettingen, Germany
6 Department of Anatomy and Cell Biology, Medical University-Varna, BG-9002 Varna, Bulgaria
2 German Center for Neurodegenerative Diseases, 37075 Goettingen, Germany
3 Max-Planck-Institute for Biophysical Chemistry, 37077 Goettingen, Germany
1 Institute of Neuroanatomy, University Medical Center, Georg-August-University, 37075 Goettingen, Germany
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  organization: Institute of Neuroanatomy, University Medical Center, Georg-August-University, 37075 Goettingen, Germany
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  organization: Max-Planck-Institute for Biophysical Chemistry, 37077 Goettingen, Germany
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  surname: Seong
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  organization: German Center for Neurodegenerative Diseases, 37075 Goettingen, Germany
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  email: tran.tuoc@med.uni-goettingen.de
  organization: Institute of Neuroanatomy, University Medical Center, Georg-August-University, 37075 Goettingen, Germany
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Keywords Molecular Neuroscience
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Snippet The abundance of basal progenitors (BPs), basal radial glia progenitors (bRGs) and basal intermediate progenitors (bIPs), in primate brain has been correlated...
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SubjectTerms Developmental Neuroscience
Molecular Neuroscience
Neuroscience
Title Chromatin Remodeling BAF155 Subunit Regulates the Genesis of Basal Progenitors in Developing Cortex
URI https://dx.doi.org/10.1016/j.isci.2018.05.014
https://www.ncbi.nlm.nih.gov/pubmed/30240734
https://www.proquest.com/docview/2111146558
https://pubmed.ncbi.nlm.nih.gov/PMC6147019
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