Frontiers in Molecular Neuroscience (Oct 2019)

Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development

  • Matías Alvarez-Saavedra,
  • Matías Alvarez-Saavedra,
  • Matías Alvarez-Saavedra,
  • Keqin Yan,
  • Yves De Repentigny,
  • Lukas E. Hashem,
  • Nidhi Chaudary,
  • Shihab Sarwar,
  • Doo Yang,
  • Doo Yang,
  • Ilya Ioshikhes,
  • Ilya Ioshikhes,
  • Rashmi Kothary,
  • Rashmi Kothary,
  • Rashmi Kothary,
  • Teruyoshi Hirayama,
  • Teruyoshi Hirayama,
  • Takeshi Yagi,
  • David J. Picketts,
  • David J. Picketts,
  • David J. Picketts

DOI
https://doi.org/10.3389/fnmol.2019.00243
Journal volume & issue
Vol. 12

Abstract

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Alterations in the homeostasis of either cortical progenitor pool, namely the apically located radial glial (RG) cells or the basal intermediate progenitors (IPCs) can severely impair cortical neuron production. Such changes are reflected by microcephaly and are often associated with cognitive defects. Genes encoding epigenetic regulators are a frequent cause of intellectual disability and many have been shown to regulate progenitor cell growth, including our inactivation of the Smarca1 gene encoding Snf2l, which is one of two ISWI mammalian orthologs. Loss of the Snf2l protein resulted in dysregulation of Foxg1 and IPC proliferation leading to macrocephaly. Here we show that inactivation of the closely related Smarca5 gene encoding the Snf2h chromatin remodeler is necessary for embryonic IPC expansion and subsequent specification of callosal projection neurons. Telencephalon-specific Smarca5 cKO embryos have impaired cell cycle kinetics and increased cell death, resulting in fewer Tbr2+ and FoxG1+ IPCs by mid-neurogenesis. These deficits give rise to adult mice with a dramatic reduction in Satb2+ upper layer neurons, and partial agenesis of the corpus callosum. Mice survive into adulthood but molecularly display reduced expression of the clustered protocadherin genes that may further contribute to altered dendritic arborization and a hyperactive behavioral phenotype. Our studies provide novel insight into the developmental function of Snf2h-dependent chromatin remodeling processes during brain development.

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