Varying Intertrial Interval Reveals Temporally Defined Memory Deficits and Enhancements in NTAN1-Deficient Mice

  1. Seth A. Balogh1,
  2. Yong Tae Kwon3, and
  3. Victor H. Denenberg1,2,4,5
  1. 1Biobehavioral Sciences Graduate Degree Program and 2Department of Psychology, University of Connecticut, Storrs, Connecticut 06269, USA; 3Division of Biology, California Institute of Technology, Pasadena, California 91125, USA

Abstract

The N-end rule is one ubiquitin-proteolytic pathway that relates the in vivo half-life of a protein to the identity of its N-terminal residue. NTAN1 deamidates N-terminal asparagine to aspartate, which is conjugated to arginine by ATE1. An N-terminal arginine-bearing substrate protein is recognized, ubiquitylated by UBR1/E3α, and subsequently degraded by 26S proteasomes. Previous research showed that NTAN1-deficient mice exhibited impaired long-term memory in the Lashley III maze. Therefore, a series of studies, designed to assess the role of NTAN1 in short- and intermediate-term memory processes, was undertaken. Two hundred sixty mice (126 −/−; 134 +/ +) received Lashley III maze training with intertrial intervals ranging from 2–180 min. Results indicated that inactivation of NTAN1 amidase differentially affects short-, intermediate-, and long-term memory.

Footnotes

  • 4 Present address: University of Connecticut, Biobehavioral Sciences, Graduate Degree Program, 3107 Horsebarn Hill Road, U-154, Storrs, CT 06269-4154, USA.

  • 5 Corresponding author.

  • E-MAIL dberg{at}uconnvm.uconn.edu; FAX (860) 486-3827.

  • Article and publication are atwww.learnmem.org/cgi/doi/10.1101/lm.33500.

    • Received May 16, 2000.
    • Accepted August 2, 2000.
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