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

AI Article Synopsis

  • Developing the central nervous system relies on tightly regulated gene expression, with Brg1 being crucial for transcription as part of the SWI/SNF chromatin remodeling complex.
  • Research found that the absence of Brg1 in neural stem cells (NSCs) between embryonic days 7.5 and 12.5 led to abnormal structures in the brain areas and significant changes in a part of the eye called the neural retina (NR).
  • Furthermore, Brg1 loss resulted in decreased cell survival and altered gene expression, indicating its specific and essential role in NSCs for proper brain and eye development.

Article 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.

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Source
http://dx.doi.org/10.1242/dev.196147DOI Listing

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