Genetic analysis of synaptotagmin 2 in spontaneous and Ca2+-triggered neurotransmitter release

被引:139
作者
Pang, Zhiping P.
Sun, Jianyuan
Rizo, Josep
Maximov, Anton
Sudhof, Thomas C.
机构
[1] UT SW Med Ctr, Howard Hughes Med Inst, Ctr Basic Neurosci, Dept Mol Genet, Dallas, TX 75390 USA
[2] UT SW Med Ctr, Howard Hughes Med Inst, Ctr Basic Neurosci, Dept Pharmacol, Dallas, TX USA
[3] UT SW Med Ctr, Howard Hughes Med Inst, Ctr Basic Neurosci, Dept Biochem, Dallas, TX USA
关键词
Calyx of Held; neuromuscular junctions; synaptic transmission; synaptotagmin;
D O I
10.1038/sj.emboj.7601103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synaptotagmin 2 resembles synaptotagmin 1, the Ca2+ sensor for fast neurotransmitter release in forebrain synapses, but little is known about synaptotagmin 2 function. Here, we describe a severely ataxic mouse strain that harbors a single, destabilizing amino-acid substitution (I377N) in synaptotagmin 2. In Calyx of Held synapses, this mutation causes a delay and a decrease in Ca2+-induced but not in hypertonic sucrose-induced release, suggesting that synaptotagmin 2 mediates Ca2+ triggering of evoked release in brainstem synapses. Unexpectedly, we additionally observed in synaptotagmin 2 mutant synapses a dramatic increase in spontaneous release. Synaptotagmin 1-deficient excitatory and inhibitory cortical synapses also displayed a large increase in spontaneous release, demonstrating that this effect was shared among synaptotagmins 1 and 2. Our data suggest that synaptotagmin 1 and 2 perform equivalent functions in the Ca2+ triggering of action potential-induced release and in the restriction of spontaneous release, consistent with a general role of synaptotagmins in controlling 'release slots' for synaptic vesicles at the active zone.
引用
收藏
页码:2039 / 2050
页数:12
相关论文
共 46 条
[1]  
Berton F, 1997, J NEUROSCI, V17, P1206
[2]   Pre- and postsynaptic whole-cell recordings in the medial nucleus of the trapezoid body of the rat [J].
Borst, JGG ;
Helmchen, F ;
Sakmann, B .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (03) :825-840
[3]   ABSENCE OF SYNAPTOTAGMIN DISRUPTS EXCITATION-SECRETION COUPLING DURING SYNAPTIC TRANSMISSION [J].
BROADIE, K ;
BELLEN, HJ ;
DIANTONIO, A ;
LITTLETON, JT ;
SCHWARZ, TL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10727-10731
[4]   THE EFFECT ON SYNAPTIC PHYSIOLOGY OF SYNAPTOTAGMIN MUTATIONS IN DROSOPHILA [J].
DIANTONIO, A ;
SCHWARZ, TL .
NEURON, 1994, 12 (04) :909-920
[5]   The tandem C2 domains of synaptotagmin contain redundant Ca2+ binding sites that cooperate to engage t-SNAREs and trigger exocytosis [J].
Earles, CA ;
Bai, JH ;
Wang, P ;
Chapman, ER .
JOURNAL OF CELL BIOLOGY, 2001, 154 (06) :1117-1123
[6]   Three-dimensional structure of the synaptotagmin 1 C2B-domain:: Synaptotagmin 1 as a phospholipid binding machine [J].
Fernandez, I ;
Araç, D ;
Ubach, J ;
Gerber, SH ;
Shin, OH ;
Gao, Y ;
Anderson, RGW ;
Südhof, TC ;
Rizo, J .
NEURON, 2001, 32 (06) :1057-1069
[7]   Synaptotagmin I functions as a calcium regulator of release probability [J].
Fernández-Chacón, R ;
Königstorfer, A ;
Gerber, SH ;
García, J ;
Matos, MF ;
Stevens, CF ;
Brose, N ;
Rizo, J ;
Rosenmund, C ;
Südhof, TC .
NATURE, 2001, 410 (6824) :41-49
[8]   A force-plate actometer for quantitating rodent behaviors: illustrative data on locomotion, rotation, spatial patterning, stereotypies, and tremor [J].
Fowler, SC ;
Birkestrand, BR ;
Chen, R ;
Moss, SJ ;
Vorontsova, E ;
Wang, G ;
Zarcone, TJ .
JOURNAL OF NEUROSCIENCE METHODS, 2001, 107 (1-2) :107-124
[9]  
FUKUDA M, 1994, J BIOL CHEM, V269, P29206
[10]  
GEPPERT M, 1991, J BIOL CHEM, V266, P13548