| Literature DB >> 28988862 |
Myeongjin Hong1, Leesun Ryu1, Maria C Ow2, Jinmahn Kim1, A Reum Je3, Satya Chinta4, Yang Hoon Huh3, Kea Joo Lee5, Rebecca A Butcher4, Hongsoo Choi6, Piali Sengupta7, Sarah E Hall2, Kyuhyung Kim8.
Abstract
Experiences during early development can influence neuronal functions and modulate adult behaviors [1, 2]. However, the molecular mechanisms underlying the long-term behavioral effects of these early experiences are not fully understood. The C. elegans ascr#3 (asc-ΔC9; C9) pheromone triggers avoidance behavior in adult hermaphrodites [3-7]. Here, we show that hermaphrodites that are briefly exposed to ascr#3 immediately after birth exhibit increased ascr#3-specific avoidance as adults, indicating that ascr#3-experienced animals form a long-lasting memory or imprint of this early ascr#3 exposure [8]. ascr#3 imprinting is mediated by increased synaptic activity between the ascr#3-sensing ADL neurons and their post-synaptic SMB motor neuron partners via increased expression of the odr-2 glycosylated phosphatidylinositol (GPI)-linked signaling gene in the SMB neurons. Our study suggests that the memory for early ascr#3 experience is imprinted via alteration of activity of a single synaptic connection, which in turn shapes experience-dependent plasticity in adult ascr#3 responses.Entities:
Keywords: GPI-anchored protein; neuronal activity; pheromone; sensory imprinting; synapse
Mesh:
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Year: 2017 PMID: 28988862 PMCID: PMC5805149 DOI: 10.1016/j.cub.2017.08.068
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834