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Mice lacking synapsin III show abnormalities in explicit memory and conditioned fear.
B Porton1, R M Rodriguiz, L E Phillips
1Department of Psychiatry and Human Behavior, Brown University, BioMedical Center, Providence, RI 02912, USA.
Genes, Brain, and Behavior
|January 7, 2010
Summary
Synapsin III knockout mice show deficits in learning and memory, particularly in object recognition and fear conditioning. These findings suggest a role for synapsin III in cognitive functions relevant to neurological disorders.
Area of Science:
- Neuroscience
- Molecular Biology
- Behavioral Genetics
Background:
- Synapsin III is a neuron-specific phosphoprotein crucial for synaptic transmission and neural development.
- Its expression is high in embryonic brain but reduced in adult brain regions like the hippocampus and cortex.
- Synapsin III is implicated in neurogenesis within the dentate gyrus.
Purpose of the Study:
- To investigate the role of synapsin III in learning and memory processes.
- To determine if synapsin III deficiency affects cognitive functions in mice.
- To explore the potential of synapsin III knockout mice as a model for studying neurological disorders.
Main Methods:
- Generation and behavioral screening of synapsin III knockout mice.
- Assessment of learning and memory using various behavioral tests, including the Morris water maze and object recognition.
- Evaluation of conditioned fear responses and fear-potentiated startle.
Main Results:
- Synapsin III knockout mice exhibited no sensory, motor, anxiety, or depressive-like behavior anomalies.
- Mutant mice showed deficits in object recognition memory at 24 hours and 10 days post-training.
- Impaired performance was observed in social transmission of food preference and various fear conditioning paradigms.
Conclusions:
- Synapsin III plays a significant role in specific learning and memory processes, including object recognition and fear memory.
- Synapsin III knockout mice present a valuable neurodevelopmental model for investigating cognitive deficits.
- These findings may offer insights into the molecular pathways underlying aspects of schizophrenia and related disorders.

