miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development

被引:52
作者
Wei, Chunyao [1 ,2 ]
Thatcher, Elizabeth J. [1 ,2 ]
Olena, Abigail F. [1 ,2 ]
Cha, Diana J. [1 ,2 ]
Perdigoto, Ana L. [2 ,3 ]
Marshall, Andrew F. [1 ,2 ]
Carter, Bruce D. [2 ,3 ]
Broadie, Kendal [1 ,2 ]
Patton, James G. [1 ,2 ]
机构
[1] Vanderbilt Univ, Dept Biol Sci, Nashville, TN 37212 USA
[2] Sch Med, Nashville, TN USA
[3] Vanderbilt Univ, Dept Biochem, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-RECEPTOR COMPLEX; T-SNARE SNAP-25; IDENTIFIED MOTONEURONS; BOTULINUM NEUROTOXIN; GENE-EXPRESSION; MEMBRANE-FUSION; AXONAL GROWTH; ZEBRAFISH DEVELOPMENT; NEURITE OUTGROWTH; PLASTICITY;
D O I
10.1371/journal.pone.0057080
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
SNAP-25 is a core component of the trimeric SNARE complex mediating vesicle exocytosis during membrane addition for neuronal growth, neuropeptide/growth factor secretion, and neurotransmitter release during synaptic transmission. Here, we report a novel microRNA mechanism of SNAP-25 regulation controlling motor neuron development, neurosecretion, synaptic activity, and movement in zebrafish. Loss of miR-153 causes overexpression of SNAP-25 and consequent hyperactive movement in early zebrafish embryos. Conversely, overexpression of miR-153 causes SNAP-25 down regulation resulting in near complete paralysis, mimicking the effects of treatment with Botulinum neurotoxin. miR-153-dependent changes in synaptic activity at the neuromuscular junction are consistent with the observed movement defects. Underlying the movement defects, perturbation of miR-153 function causes dramatic developmental changes in motor neuron patterning and branching. Together, our results indicate that precise control of SNAP-25 expression by miR-153 is critically important for proper neuronal patterning as well as neurotransmission.
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页数:14
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