4.8 Article

Early Pheromone Experience Modifies a Synaptic Activity to Influence Adult Pheromone Responses of C. elegans

期刊

CURRENT BIOLOGY
卷 27, 期 20, 页码 3168-+

出版社

CELL PRESS
DOI: 10.1016/j.cub.2017.08.068

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资金

  1. Ministry of Science, ICT and Future Planning [17-BD-06, 17-BR-04, 17-BR-02]
  2. National Research Foundation of Korea [NRF-2015R1D1A1A09061430, NRF-2017R1A4A1015534]
  3. NIH [R15GM111094, R01GM087533]
  4. NSF IOS [1256488, 1655118]
  5. KBSI [T37416]
  6. Ministry for Health and Welfare [HI14C1135]
  7. Ministry of Science & ICT (MSIT), Republic of Korea [17-BR-04, 17-BR-02, 17-BD-06] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. Division Of Integrative Organismal Systems
  9. Direct For Biological Sciences [1655118, 1256488] Funding Source: National Science Foundation

向作者/读者索取更多资源

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-Delta C9; 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.

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