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ZBTB20 is crucial for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex.
Medeiros de Araújo, Jéssica Alves; Barão, Soraia; Mateos-White, Isabel; Espinosa, Ana; Costa, Marcos Romualdo; Gil-Sanz, Cristina; Müller, Ulrich.
  • Medeiros de Araújo JA; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Barão S; Brain Institute, Federal University of Rio Grande do Norte, Natal, RN 59056-450, Brazil.
  • Mateos-White I; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Espinosa A; BIOTECMED Institute, Universidad de Valencia, Burjassot, Valencia 46100, Spain.
  • Costa MR; AntalGenics, Quorum Building III, Scientific Park - UMH. Avda. de la Universidad, s/n. 03202 Elche (Alicante), Spain.
  • Gil-Sanz C; Brain Institute, Federal University of Rio Grande do Norte, Natal, RN 59056-450, Brazil.
  • Müller U; Unité INSERM 1167, RID-AGE-Risk Factors and Molecular Determinants of Aging-Related Diseases, Institut Pasteur de Lille, University of Lille, U1167-Excellence Laboratory LabEx DISTALZ, Lille Cedex 59019, France.
Development ; 148(16)2021 08 15.
Article en En | MEDLINE | ID: mdl-34351428
ABSTRACT
Neocortical progenitor cells generate subtypes of excitatory projection neurons in sequential order followed by the generation of astrocytes. The transcription factor zinc finger and BTB domain-containing protein 20 (ZBTB20) has been implicated in regulation of cell specification during neocortical development. Here, we show that ZBTB20 instructs the generation of a subset of callosal projections neurons in cortical layers II/III in mouse. Conditional deletion of Zbtb20 in cortical progenitors, and to a lesser degree in differentiating neurons, leads to an increase in the number of layer IV neurons at the expense of layer II/III neurons. Astrogliogenesis is also affected in the mutants with an increase in the number of a specific subset of astrocytes expressing GFAP. Astrogliogenesis is more severely disrupted by a ZBTB20 protein containing dominant mutations linked to Primrose syndrome, suggesting that ZBTB20 acts in concert with other ZBTB proteins that were also affected by the dominant-negative protein to instruct astrogliogenesis. Overall, our data suggest that ZBTB20 acts both in progenitors and in postmitotic cells to regulate cell fate specification in the mammalian neocortex.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Astrocitos / Neocórtex / Neurogénesis / Neuronas Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Astrocitos / Neocórtex / Neurogénesis / Neuronas Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article