Liu Huisheng, Bai Hua, Hui Enfu, Yang Lu, Evans Chantell S, Wang Zhao, Kwon Sung E, Chapman Edwin R
Department of Neuroscience, Howard Hughes Medical Institute, University of Wisconsin-Madison, Madison, United States.
Elife. 2014 Feb 25;3:e01524. doi: 10.7554/eLife.01524.
Synaptotagmin (syt) 7 is one of three syt isoforms found in all metazoans; it is ubiquitously expressed, yet its function in neurons remains obscure. Here, we resolved Ca(2+)-dependent and Ca(2+)-independent synaptic vesicle (SV) replenishment pathways, and found that syt 7 plays a selective and critical role in the Ca(2+)-dependent pathway. Mutations that disrupt Ca(2+)-binding to syt 7 abolish this function, suggesting that syt 7 functions as a Ca(2+)-sensor for replenishment. The Ca(2+)-binding protein calmodulin (CaM) has also been implicated in SV replenishment, and we found that loss of syt 7 was phenocopied by a CaM antagonist. Moreover, we discovered that syt 7 binds to CaM in a highly specific and Ca(2+)-dependent manner; this interaction requires intact Ca(2+)-binding sites within syt 7. Together, these data indicate that a complex of two conserved Ca(2+)-binding proteins, syt 7 and CaM, serve as a key regulator of SV replenishment in presynaptic nerve terminals. DOI: http://dx.doi.org/10.7554/eLife.01524.001.
突触结合蛋白(syt)7是在后生动物中发现的三种syt亚型之一;它在全身广泛表达,但其在神经元中的功能仍不清楚。在这里,我们解析了依赖钙和不依赖钙的突触小泡(SV)补充途径,发现syt 7在依赖钙的途径中发挥着选择性和关键作用。破坏syt 7与钙结合的突变会消除这一功能,表明syt 7作为补充过程中的钙传感器发挥作用。钙结合蛋白钙调蛋白(CaM)也与SV补充有关,我们发现syt 7的缺失可被CaM拮抗剂模拟。此外,我们发现syt 7以高度特异性和依赖钙的方式与CaM结合;这种相互作用需要syt 7内完整的钙结合位点。总之,这些数据表明,两种保守的钙结合蛋白syt 7和CaM的复合物是突触前神经末梢中SV补充的关键调节因子。DOI: http://dx.doi.org/10.7554/eLife.01524.001 。