Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 15 May 2009:
Vol. 324. no. 5929, pp. 904 - 909
DOI: 10.1126/science.1171498

Research Articles

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

Daisuke Okada,* Fumiko Ozawa, Kaoru Inokuchi*

Late-phase synaptic plasticity depends on the synthesis of new proteins that must function only in the activated synapses. The synaptic tag hypothesis requires input-specific functioning of these proteins after undirected transport. Confirmation of this hypothesis requires specification of a biochemical tagging activity and an example protein that behaves as the hypothesis predicts. We found that in rat neurons, soma-derived Vesl-1S (Homer-1a) protein, a late-phase plasticity-related synaptic protein, prevailed in every dendrite and did not enter spines. N-methyl-D-aspartate receptor activation triggered input-specific spine entry of Vesl-1S proteins, which met many criteria for synaptic tagging. These results suggest that Vesl-1S supports the hypothesis and that the activity-dependent regulation of spine entry functions as a synaptic tag.

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.

* To whom correspondence should be addressed. E-mail: kaoru{at}mitils.jp (K.I.); dada{at}mitils.jp (D.O.)

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Bridging the Gap and Staying Local.
M. Korte (2009)
Science 324, 1527-1528
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)