ZBTB20 is crucial for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex

Author:

Medeiros de Araújo Jéssica Alves12,Barão Soraia1,Mateos-White Isabel3,Espinosa Ana4,Costa Marcos Romualdo25,Gil-Sanz Cristina3ORCID,Müller Ulrich1

Affiliation:

1. The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

2. Brain Institute, Federal University of Rio Grande do Norte, Natal, RN 59056-450, Brazil

3. BIOTECMED Institute, Universidad de Valencia, Burjassot, Valencia 46100, Spain

4. AntalGenics, Quorum Building III, Scientific Park - UMH. Avda. de la Universidad, s/n. 03202 Elche (Alicante), Spain

5. 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

Abstract

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.

Funder

National Institute of Mental Health

Ministerio de Ciencia e Innovación

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselleria de Educación de Valencia

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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