Brahma-related gene 1 has time-specific roles during brain and eye development

Author:

Holdhof Dörthe12ORCID,Schoof Melanie12,Al-Kershi Sina12,Spohn Michael23,Kresbach Catena12,Göbel Carolin12,Hellwig Malte12,Indenbirken Daniela4,Moreno Natalia5,Kerl Kornelius5,Schüller Ulrich126ORCID

Affiliation:

1. Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

2. Research Institute Children's Cancer Center Hamburg, 20251 Hamburg, Germany

3. Bioinformatics Facility, University Medical Center, Hamburg-Eppendorf, 20246 Hamburg, Germany

4. Heinrich-Pette-Institute, Leibniz Institute for Experimental Virology, 20251 Hamburg, Germany

5. Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48149 Münster, Germany

6. Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

Abstract

ABSTRACT During development, gene expression is tightly controlled to facilitate the generation of the diverse cell types that form the central nervous system. Brahma-related gene 1 (Brg1, also known as Smarca4) is the catalytic subunit of the SWItch/sucrose nonfermentable (SWI/SNF) chromatin remodeling complex that regulates transcription. We investigated the role of Brg1 between embryonic day 6.5 (E6.5) and E14.5 in Sox2-positive neural stem cells (NSCs). Being without major consequences at E6.5 and E14.5, loss of Brg1 between E7.5 and E12.5 resulted in the formation of rosette-like structures in the subventricular zone, as well as morphological alterations and enlargement of neural retina (NR). Additionally, Brg1-deficient cells showed decreased survival in vitro and in vivo. Furthermore, we uncovered distinct changes in gene expression upon Brg1 loss, pointing towards impaired neuron functions, especially those involving synaptic communication and altered composition of the extracellular matrix. Comparison with mice deficient for integrase interactor 1 (Ini1, also known as Smarcb1) revealed that the enlarged NR was Brg1 specific and was not caused by a general dysfunction of the SWI/SNF complex. These results suggest a crucial role for Brg1 in NSCs during brain and eye development.

Funder

Deutsche Krebshilfe

Wilhelm Sander Stiftung

Fördergemeinschaft Kinderkrebszentrum Hamburg

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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