Input-Specific Spine Entry of Soma-Derived Vesl-1S Protein Conforms to Synaptic Tagging

Author:

Okada Daisuke1,Ozawa Fumiko1,Inokuchi Kaoru1

Affiliation:

1. Mitsubishi Kagaku Institute of Life Sciences (MITILS), 11 Minamiooya, Machida, Tokyo 194-8511, Japan, and Japan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST), 4-1-8 Honcho, Kawaguchi 332-0012, Japan.

Abstract

Synaptic Tag Tagged Input-dependent synaptic plasticity is critical for the reproducible activation of a specific neuronal assembly encoding a particular memory. The synaptic tagging hypothesis, which suggests how input specificity is maintained in late-phase synaptic plasticity, attempts to explain the persistence of long-term memory. However, it has been difficult to identify proteins that behave as the hypothesis predicts. Okada et al. (p. 904 ) investigated if the regulated spine entry of a late-phase-related somatically synthesized plasticity-related protein, Vesl-1S, works as a synaptic tag. Vesl-1S protein was carried from the soma to every dendrite and recruited into spines by synaptic activation in an input-specific manner. Spine entry was protein-synthesis independent, was NMDA receptor dependent, and had a persistent lifetime of activation. These results provide long-sought evidence for the input-specific capturing of a plasticity-related protein as postulated by the synaptic tagging hypothesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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