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The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
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Related Experiment Video

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Assessment of Sexual Behavior of Male Mice
04:38

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Published on: March 5, 2020

Abnormal behavior in mice mutant for the Disc1 binding partner, Dixdc1.

S Kivimäe1, P-M Martin, D Kapfhamer

  • 1Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94158, USA.

Translational Psychiatry
|July 27, 2012
PubMed
Summary
This summary is machine-generated.

Mice lacking the DIX domain containing 1 (Dixdc1) gene showed abnormal behaviors, including reduced activity and altered startle responses. These findings suggest Dixdc1

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Generation, Purification, and Characterization of Cell-invasive DISC1 Protein Species
14:33

Generation, Purification, and Characterization of Cell-invasive DISC1 Protein Species

Published on: August 30, 2012

Area of Science:

  • Neuroscience
  • Genetics
  • Molecular Biology

Background:

  • Disrupted-in-Schizophrenia-1 (DISC1) is a key genetic factor in schizophrenia and depression.
  • DISC1 interacts with DIX domain containing 1 (Dixdc1), influencing neural progenitor proliferation and migration.
  • Both DISC1 and Dixdc1 are implicated in Wnt signaling pathways crucial for neural development.

Purpose of the Study:

  • To investigate the behavioral consequences of Dixdc1 gene mutations in mice.
  • To explore the potential role of Dixdc1 in the pathophysiology of major mental illnesses.
  • To establish Dixdc1 mutant mice as a model for studying DISC1-related disorders.

Main Methods:

  • Generation of Dixdc1 knockout (Dixdc1(-/-)) mice.
  • Behavioral analysis including prepulse inhibition, locomotor activity, elevated plus maze, and startle reactivity.
  • Comparison of Dixdc1(-/-) mice with wild-type controls.

Main Results:

  • Dixdc1(-/-) mice exhibited normal prepulse inhibition.
  • Significant decreases in spontaneous locomotor activity were observed.
  • Abnormal behaviors in the elevated plus maze and deficits in startle reactivity were noted.

Conclusions:

  • Dixdc1 plays a role in regulating specific behaviors relevant to mental health.
  • Dixdc1(-/-) mice represent a valuable model for investigating the molecular mechanisms underlying DISC1-associated mental illnesses.
  • Further research using this model can elucidate the pathophysiology of schizophrenia and depression.