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The transcription factor odd-paired regulates temporal identity in transit-amplifying neural progenitors via an incoherent feed-forward loop.
Abdusselamoglu, Merve Deniz; Eroglu, Elif; Burkard, Thomas R; Knoblich, Jürgen A.
Affiliation
  • Abdusselamoglu MD; IMBA - Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna Biocenter (VBC), Vienna, Austria.
  • Eroglu E; IMBA - Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna Biocenter (VBC), Vienna, Austria.
  • Burkard TR; IMBA - Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna Biocenter (VBC), Vienna, Austria.
  • Knoblich JA; IMBA - Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna Biocenter (VBC), Vienna, Austria.
Elife ; 82019 07 22.
Article de En | MEDLINE | ID: mdl-31329099
ABSTRACT
Neural progenitors undergo temporal patterning to generate diverse neurons in a chronological order. This process is well-studied in the developing Drosophila brain and conserved in mammals. During larval stages, intermediate neural progenitors (INPs) serially express Dichaete (D), grainyhead (Grh) and eyeless (Ey/Pax6), but how the transitions are regulated is not precisely understood. Here, we developed a method to isolate transcriptomes of INPs in their distinct temporal states to identify a complete set of temporal patterning factors. Our analysis identifies odd-paired (opa), as a key regulator of temporal patterning. Temporal patterning is initiated when the SWI/SNF complex component Osa induces D and its repressor Opa at the same time but with distinct kinetics. Then, high Opa levels repress D to allow Grh transcription and progress to the next temporal state. We propose that Osa and its target genes opa and D form an incoherent feedforward loop (FFL) and a new mechanism allowing the successive expression of temporal identities.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription / Encéphale / Protéines à homéodomaine / Régulation de l'expression des gènes au cours du développement / Protéines de Drosophila / Protéines de liaison à l'ADN / Drosophila / Facteurs de transcription SOX / Cellules souches neurales Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Elife Année: 2019 Type de document: Article Pays d'affiliation: Autriche

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription / Encéphale / Protéines à homéodomaine / Régulation de l'expression des gènes au cours du développement / Protéines de Drosophila / Protéines de liaison à l'ADN / Drosophila / Facteurs de transcription SOX / Cellules souches neurales Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Elife Année: 2019 Type de document: Article Pays d'affiliation: Autriche