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Volume 8 Issue 6, June 2005

Activity-dependent signaling from the synapse to the nucleus is important for synaptic plasticity and neuronal survival. David Ginty and colleagues generated conditional knockout mice for serum response factor (SRF), a candidate transcriptional regulator of activity-induced gene expression, and compared their phenotype with that of mice lacking CREB family transcription factors. CREB mutants showed neuronal degeneration, whereas the SRF mutants had synaptic plasticity deficits. Thus the authors suggest that these factors regulate distinct gene-expression programs that make differing contributions to survival and plasticity in mature neurons. (p 759)

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  • How do genes act in the brain to influence susceptibility to mental illness? An imaging study suggests that healthy carriers of a gene variant associated with depression risk have decreased brain volume and neural coupling in affective circuitry involved in depression.

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  • How do we form arbitrary associations, such as 'stop at red' or 'go at green'? A report in Nature suggests that these associations are first formed in the striatum but that activity changes in the prefrontal cortex are more closely related to improved performance.

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    • Barry J Richmond
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