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Disrupted-in-schizophrenia 1 regulates transport of ITPR1 mRNA for synaptic plasticity.

Daisuke TsuboiKeisuke KurodaMotoki TanakaTakashi NambaYukihiko IizukaShinichiro TayaTomoyasu ShinodaTakao HikitaShinsuke MuraokaMichiro IizukaAi NimuraAkira MizoguchiNobuyuki ShiinaMasahiro SokabeHideyuki OkanoKatsuhiko MikoshibaKozo Kaibuchi
Published in: Nature neuroscience (2015)
Disrupted-in-schizophrenia 1 (DISC1) is a susceptibility gene for major psychiatric disorders, including schizophrenia. DISC1 has been implicated in neurodevelopment in relation to scaffolding signal complexes. Here we used proteomic analysis to screen for DISC1 interactors and identified several RNA-binding proteins, such as hematopoietic zinc finger (HZF), that act as components of RNA-transporting granules. HZF participates in the mRNA localization of inositol-1,4,5-trisphosphate receptor type 1 (ITPR1), which plays a key role in synaptic plasticity. DISC1 colocalizes with HZF and ITPR1 mRNA in hippocampal dendrites and directly associates with neuronal mRNAs, including ITPR1 mRNA. The binding potential of DISC1 for ITPR1 mRNA is facilitated by HZF. Studies of Disc1-knockout mice have revealed that DISC1 regulates the dendritic transport of Itpr1 mRNA by directly interacting with its mRNA. The DISC1-mediated mRNA regulation is involved in synaptic plasticity. We show that DISC1 binds ITPR1 mRNA with HZF, thereby regulating its dendritic transport for synaptic plasticity.
Keyphrases
  • binding protein
  • bipolar disorder
  • dna methylation
  • gene expression
  • genome wide
  • high throughput
  • risk assessment
  • transcription factor
  • blood brain barrier
  • cerebral ischemia
  • nucleic acid
  • case control