Mechanism of Psychiatric Disorder Agent Identified

Mechanism of Psychiatric Disorder Agent Identified

by Chrisy Ngilneii on  December 18, 2017 at 3:19 PM Health Watch
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Highlights:
  • New mechanism of psychiatric disorder agents has been identified.
  • These agents are proteins known as DISC1 and Ndel1.
  • Mechanism points to the role of genetic insults in psychiatric disorders.
New mechanism of protein DISC1 identified
A new mechanism of action for protein DISC1 based on its structure, which can lead to implications for how genetic insults may contribute to psychiatric disorders has been identified by recent research at the Hong Kong University of Science and Technology in a close collaboration with a team from the Perelman School for Medicine, University of Pennsylvania.
Mechanism of Psychiatric Disorder Agent Identified

DISC1 (disrupted-in-schizophrenia 1), originally identified in a large Scottish family suffering from multiple psychiatric disorders due to a chromosomal translocation-induced disruption, has been established as a genetic risk factor for a wide array of psychiatric disorders, including schizophrenia, bipolar disorder, major depression, and autism spectrum disorders. Unmatched to the wealth of functional and pathological data on DISC1, biochemical and structural characterizations of DISC1 and its interactions with target proteins are very scarce.

"Our study revealed that mechanistically, DISC1 regulates Ndel1's kinetochore attachment, but not its centrosome localization, during mitosis," said Professor Zhang Mingjie, Kerry Holdings Professor of Science and leader of the research group.

DISC1/Ndel1 and cell progression
"Functionally, disrupting DISC1/Ndel1 complex formation prolongs mitotic length and interferes with cell-cycle progression in human cells, and it causes cell-cycle deficits of neuronal stem cells in the embryonic mouse cortex and human forebrain organoids. We also observed similar deficits in organoids derived from schizophrenia patient induced pluripotent stem cells (iPSCs) with a DISC1 mutation that disrupts its interaction with Ndel1." Professor Zhang further added: "This is a multifaceted research effort spanning very broad research areas and taking about eight years to complete. We are especially thankful to our collaborators from the University of Pennsylvania, who have contributed much to the functional aspects of the paper using human brain organoids as the model system."

Genetic insults may cause psychiatric disorders
"The findings uncovered a new mechanism of action for DISC1 based on its structure and have implications for how genetic insults may contribute to psychiatric disorders," said Ye Fei, a leading author of the paper. "We characterized the binding properties between DISC1 and Ndel1. This structural insight into the DISC1/Ndel1 complex allowed us to develop a highly specific approach to study the function of their interaction by designing a highly specific peptide, which only inhibits the formation of the DISC1/Ndel1 complex but does not interfere with the bindings of these two proteins to many other target proteins."

"Based on structural insights, we identified a function of DISC1/Ndel1 interaction in regulating cell-cycle progression of neuronal stem cells in an animal model and in human forebrain organoids," said Professor Zhang. "Our study from patient-derived forebrain organoids provides a potential mechanistic understanding of how DISC1 mutation with its C-terminal deletion can affect neural developmental processes, and insight into mechanisms of pathogenesis of complex psychiatric disorders."

References:
  1. Fei Ye,Eunchai Kang et al. DISC1 Regulates Neurogenesis via Modulating Kinetochore Attachment of Ndel1/Nde1 during Mitosis, Journal DOI: http://dx.doi.org/10.1016/j.neuron.2017.10.010


Source-Eurekalert

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