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 in | Cell reports (Cambridge) Vol. 17; no. 2; pp. 469 - 483 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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04.10.2016
Cell Press Elsevier |
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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.
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•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. |
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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 |
AuthorAffiliation_xml | – name: 2 Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy – name: 1 Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – name: 3 Department of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden |
Author_xml | – sequence: 1 givenname: Francisca F. surname: Vasconcelos fullname: Vasconcelos, Francisca F. organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – sequence: 2 givenname: Alessandro surname: Sessa fullname: Sessa, Alessandro organization: Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy – sequence: 3 givenname: Cátia surname: Laranjeira fullname: Laranjeira, Cátia organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – sequence: 4 givenname: Alexandre A.S.F. surname: Raposo fullname: Raposo, Alexandre A.S.F. organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – sequence: 5 givenname: Vera surname: Teixeira fullname: Teixeira, Vera organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – sequence: 6 givenname: Daniel W. surname: Hagey fullname: Hagey, Daniel W. organization: Department of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden – sequence: 7 givenname: Diogo M. surname: Tomaz fullname: Tomaz, Diogo M. organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal – sequence: 8 givenname: Jonas surname: Muhr fullname: Muhr, Jonas organization: Department of Cell and Molecular Biology, Ludwig Institute for Cancer Research, Karolinska Institutet, 17177 Stockholm, Sweden – sequence: 9 givenname: Vania surname: Broccoli fullname: Broccoli, Vania organization: Division of Neuroscience, San Raffaele Scientific Institute, 20132 Milan, Italy – sequence: 10 givenname: Diogo S. surname: Castro fullname: Castro, Diogo S. email: dscastro@igc.gulbenkian.pt organization: Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal |
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Keywords | transcription Notch signaling neurogenesis Hes1 Rbpj MyT1 Ascl1 |
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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 |
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