The ubiquitin-specific protease 14 (USP14) is a critical regulator of long-term memory formation

Learn Mem. 2013 Dec 16;21(1):9-13. doi: 10.1101/lm.032771.113.

Abstract

Numerous studies have suggested a role for ubiquitin-proteasome-mediated protein degradation in learning-dependent synaptic plasticity; however, very little is known about how protein degradation is regulated at the level of the proteasome during memory formation. The ubiquitin-specific protease 14 (USP14) is a proteasomal deubiquitinating enzyme that is thought to regulate protein degradation in neurons; however, it is unknown if USP14 is involved in learning-dependent synaptic plasticity. We found that infusion of a USP14 inhibitor into the amygdala impaired long-term memory for a fear conditioning task, suggesting that USP14 is a critical regulator of long-term memory formation in the amygdala.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acoustic Stimulation / adverse effects
  • Amygdala / metabolism*
  • Analysis of Variance
  • Animals
  • Conditioning, Classical / drug effects
  • Conditioning, Classical / physiology
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / toxicity
  • Fear* / drug effects
  • Male
  • Memory Disorders / chemically induced
  • Memory, Long-Term / drug effects
  • Memory, Long-Term / physiology*
  • Rats
  • Rats, Long-Evans
  • Ubiquitin Thiolesterase / metabolism*

Substances

  • Enzyme Inhibitors
  • Ubiquitin Thiolesterase