4.8 Article

Disrupted-in-schizophrenia 1 regulates integration of newly generated neurons in the adult brain

Journal

CELL
Volume 130, Issue 6, Pages 1146-1158

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2007.07.010

Keywords

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Funding

  1. NIA NIH HHS [AG024984, R01 AG024984, R01 AG024984-04] Funding Source: Medline
  2. NICHD NIH HHS [HD045757, R01 HD045757, R01 HD069184] Funding Source: Medline
  3. NINDS NIH HHS [R56 NS047344, R37 NS047344, R01 NS047344-05, R01 NS048271, R01 NS047344, NS047344, NS048271, R01 NS048271-04] Funding Source: Medline

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Adult neurogenesis occurs throughout life in discrete regions of the adultmammalian brain. Little is known about the mechanism governing the sequential developmental process that leads to integration of new neurons from adult neural stem cells into the existing circuitry. Here, we investigated roles of Disrupted- In- Schizophrenia 1 ( DISC1), a schizophrenia susceptibility gene, in adult hippocampal neurogenesis. Unexpectedly, downregulation of DISC1 leads to accelerated neuronal integration, resulting in aberrant morphological development and mispositioning of new dentate granule cells in a cell- autonomous fashion. Functionally, newborn neurons with DISC1 knockdown exhibit enhanced excitability and accelerated dendritic development and synapse formation. Furthermore, DISC1 cooperates with its binding partner NDEL1 in regulating adult neurogenesis. Taken together, our study identifies DISC1 as a key regulator that orchestrates the tempo of functional neuronal integration in the adult brain and demonstrates essential roles of a susceptibility gene for major mental illness in neuronal development, including adult neurogenesis.

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