Otology Laboratory, Department of Otolaryngology - Head and Neck Surgery, University of South Florida, College of Medicine, Tampa, Florida, United States of America.
PLoS One. 2011;6(12):e28532. doi: 10.1371/journal.pone.0028532. Epub 2011 Dec 9.
The large-conductance Ca(2+)-activated K(+) (BK) channel and its β-subunit underlie tuning in non-mammalian sensory or hair cells, whereas in mammals its function is less clear. To gain insights into species differences and to reveal putative BK functions, we undertook a systems analysis of BK and BK-Associated Proteins (BKAPS) in the chicken cochlea and compared these results to other species. We identified 110 putative partners from cytoplasmic and membrane/cytoskeletal fractions, using a combination of coimmunoprecipitation, 2-D gel, and LC-MS/MS. Partners included 14-3-3γ, valosin-containing protein (VCP), stathmin (STMN), cortactin (CTTN), and prohibitin (PHB), of which 16 partners were verified by reciprocal coimmunoprecipitation. Bioinformatics revealed binary partners, the resultant interactome, subcellular localization, and cellular processes. The interactome contained 193 proteins involved in 190 binary interactions in subcellular compartments such as the ER, mitochondria, and nucleus. Comparisons with mice showed shared hub proteins that included N-methyl-D-aspartate receptor (NMDAR) and ATP-synthase. Ortholog analyses across six species revealed conserved interactions involving apoptosis, Ca(2+) binding, and trafficking, in chicks, mice, and humans. Functional studies using recombinant BK and RNAi in a heterologous expression system revealed that proteins important to cell death/survival, such as annexinA5, γ-actin, lamin, superoxide dismutase, and VCP, caused a decrease in BK expression. This revelation led to an examination of specific kinases and their effectors relevant to cell viability. Sequence analyses of the BK C-terminus across 10 species showed putative binding sites for 14-3-3, RAC-α serine/threonine-protein kinase 1 (Akt), glycogen synthase kinase-3β (GSK3β) and phosphoinositide-dependent kinase-1 (PDK1). Knockdown of 14-3-3 and Akt caused an increase in BK expression, whereas silencing of GSK3β and PDK1 had the opposite effect. This comparative systems approach suggests conservation in BK function across different species in addition to novel functions that may include the initiation of signals relevant to cell death/survival.
大电导钙激活钾(BK)通道及其β亚基是调节非哺乳动物感觉或毛细胞功能的基础,而在哺乳动物中其功能尚不清楚。为了深入了解物种差异并揭示潜在的 BK 功能,我们对鸡耳蜗中的 BK 和 BK 相关蛋白(BKAPs)进行了系统分析,并将这些结果与其他物种进行了比较。我们使用免疫共沉淀、二维凝胶电泳和 LC-MS/MS 相结合的方法,从细胞质和膜/细胞骨架部分鉴定了 110 种潜在的伴侣蛋白。这些伴侣蛋白包括 14-3-3γ、含缬氨酸蛋白(VCP)、微管蛋白稳定蛋白(STMN)、桩蛋白(CTTN)和抑素(PHB),其中 16 个伴侣蛋白通过相互免疫沉淀得到验证。生物信息学分析揭示了二元相互作用、相互作用网络、亚细胞定位和细胞过程。该相互作用网络包含 193 种蛋白质,涉及 ER、线粒体和细胞核等亚细胞区室的 190 个二元相互作用。与小鼠的比较显示,包括 N-甲基-D-天冬氨酸受体(NMDAR)和 ATP 合酶在内的共享枢纽蛋白。六个物种的同源分析显示,涉及细胞凋亡、Ca2+结合和运输的保守相互作用在小鸡、小鼠和人类中存在。在异源表达系统中使用重组 BK 和 RNAi 进行的功能研究表明,对细胞死亡/存活很重要的蛋白质,如 annexinA5、γ-肌动蛋白、层粘连蛋白、超氧化物歧化酶和 VCP,会导致 BK 表达减少。这一发现促使我们研究与细胞活力相关的特定激酶及其效应物。对 10 种物种的 BK C 末端进行序列分析显示,存在与 14-3-3、RAC-α 丝氨酸/苏氨酸蛋白激酶 1(Akt)、糖原合成酶激酶-3β(GSK3β)和磷酸肌醇依赖性激酶-1(PDK1)结合的假定结合位点。敲低 14-3-3 和 Akt 导致 BK 表达增加,而沉默 GSK3β 和 PDK1 则产生相反的效果。这种比较系统的方法表明,BK 功能在不同物种中是保守的,除了可能包括与细胞死亡/存活相关的信号起始的新功能之外。