Varying intertrial interval reveals temporally defined memory deficits and enhancements in NTAN1-deficient mice |
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Authors: | Balogh S A Kwon Y T Denenberg V H |
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Affiliation: | Biobehavioral Sciences Graduate Degree Program, University of Connecticut, Storrs, Connecticut 06269, USA. |
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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. |
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