Varying intertrial interval reveals temporally defined memory deficits and enhancements in NTAN1-deficient mice

被引:27
作者
Balogh, SA
Kwon, YT
Denenberg, VH
机构
[1] Univ Connecticut, Biobehav Sci Grad Degree Program, Storrs, CT 06269 USA
[2] Univ Connecticut, Dept Psychol, Storrs, CT 06269 USA
[3] CALTECH, Div Biol, Pasadena, CA 91125 USA
关键词
D O I
10.1101/lm.33500
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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/E3 alpha, 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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收藏
页码:279 / 286
页数:8
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