MyT1 Counteracts the Neural Progenitor Program to Promote Vertebrate Neurogenesis

The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on...

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Published inCell reports (Cambridge) Vol. 17; no. 2; pp. 469 - 483
Main Authors Vasconcelos, Francisca F., Sessa, Alessandro, Laranjeira, Cátia, Raposo, Alexandre A.S.F., Teixeira, Vera, Hagey, Daniel W., Tomaz, Diogo M., Muhr, Jonas, Broccoli, Vania, Castro, Diogo S.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 04.10.2016
Cell Press
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Abstract The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1, Sox2, Id3, and Olig1. Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate. [Display omitted] •MyT1 promotes neurogenesis downstream Ascl1•MyT1 represses Notch1 receptor and many of its downstream target genes•MyT1 represses Hes1 expression by direct DNA binding and competition with RBPJ•Ascl1 suppresses Notch signaling cell-autonomously while promoting differentiation Vasconcelos et al. find that the transcription factor MyT1 promotes neuronal differentiation downstream the proneural factor Ascl1. MyT1 represses the transcription of Notch signaling components and targets genes, including important regulators of the neural progenitor program. Thus, Ascl1 activates differentiation genes while repressing the progenitor program via MyT1.
AbstractList The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1, Sox2, Id3, and Olig1. Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate.
The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1, Sox2, Id3, and Olig1. Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate.
The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1 , Sox2 , Id3 , and Olig1 . Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate. • MyT1 promotes neurogenesis downstream Ascl1 • MyT1 represses Notch1 receptor and many of its downstream target genes • MyT1 represses Hes1 expression by direct DNA binding and competition with RBPJ • Ascl1 suppresses Notch signaling cell-autonomously while promoting differentiation Vasconcelos et al. find that the transcription factor MyT1 promotes neuronal differentiation downstream the proneural factor Ascl1. MyT1 represses the transcription of Notch signaling components and targets genes, including important regulators of the neural progenitor program. Thus, Ascl1 activates differentiation genes while repressing the progenitor program via MyT1.
The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural transcription factors, such as Ascl1. While recent studies have characterized the differentiation genes activated by proneural factors, less is known on the mechanisms that suppress progenitor cell identity. Here, we show that Ascl1 induces the transcription factor MyT1 while promoting neuronal differentiation. We combined functional studies of MyT1 during neurogenesis with the characterization of its transcriptional program. MyT1 binding is associated with repression of gene transcription in neural progenitor cells. It promotes neuronal differentiation by counteracting the inhibitory activity of Notch signaling at multiple levels, targeting the Notch1 receptor and many of its downstream targets. These include regulators of the neural progenitor program, such as Hes1, Sox2, Id3, and Olig1. Thus, Ascl1 suppresses Notch signaling cell-autonomously via MyT1, coupling neuronal differentiation with repression of the progenitor fate. [Display omitted] •MyT1 promotes neurogenesis downstream Ascl1•MyT1 represses Notch1 receptor and many of its downstream target genes•MyT1 represses Hes1 expression by direct DNA binding and competition with RBPJ•Ascl1 suppresses Notch signaling cell-autonomously while promoting differentiation Vasconcelos et al. find that the transcription factor MyT1 promotes neuronal differentiation downstream the proneural factor Ascl1. MyT1 represses the transcription of Notch signaling components and targets genes, including important regulators of the neural progenitor program. Thus, Ascl1 activates differentiation genes while repressing the progenitor program via MyT1.
Author Laranjeira, Cátia
Vasconcelos, Francisca F.
Castro, Diogo S.
Teixeira, Vera
Muhr, Jonas
Hagey, Daniel W.
Sessa, Alessandro
Raposo, Alexandre A.S.F.
Broccoli, Vania
Tomaz, Diogo M.
AuthorAffiliation 1 Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal
2 Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy
3 Department of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden
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Issue 2
Keywords transcription
Notch signaling
neurogenesis
Hes1
Rbpj
MyT1
Ascl1
Language English
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Snippet The generation of neurons from neural stem cells requires large-scale changes in gene expression that are controlled to a large extent by proneural...
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SubjectTerms Animals
Ascl1
Basic Helix-Loop-Helix Transcription Factors - genetics
Cell Differentiation - genetics
DNA-Binding Proteins - genetics
Gene Expression Regulation, Developmental
Hes1
Inhibitor of Differentiation Proteins - genetics
Mice
MyT1
Neural Stem Cells - cytology
Neural Stem Cells - metabolism
neurogenesis
Neurogenesis - genetics
Neurons - metabolism
Notch signaling
Rbpj
Receptor, Notch1 - genetics
SOXB1 Transcription Factors - genetics
Stem Cells - cytology
Stem Cells - metabolism
transcription
Transcription Factor HES-1 - genetics
Transcription Factors - genetics
Vertebrates - genetics
Vertebrates - growth & development
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Title MyT1 Counteracts the Neural Progenitor Program to Promote Vertebrate Neurogenesis
URI https://dx.doi.org/10.1016/j.celrep.2016.09.024
https://www.ncbi.nlm.nih.gov/pubmed/27705795
https://www.proquest.com/docview/1835361896
https://pubmed.ncbi.nlm.nih.gov/PMC5067283
http://kipublications.ki.se/Default.aspx?queryparsed=id:134390757
https://doaj.org/article/33b0f2cdd32244e3a144359259560abd
Volume 17
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