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首页> 外文期刊>The Plant Cell >Ca2+-dependent protein kinase11 and 24 modulate the activity of the inward rectifying K+ channels in Arabidopsis pollen tubes.
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Ca2+-dependent protein kinase11 and 24 modulate the activity of the inward rectifying K+ channels in Arabidopsis pollen tubes.

机译:Ca 2 + 依赖性蛋白激酶11和24调节拟南芥花粉管内向整流K + 通道的活性。

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Potassium (K+) influx into pollen tubes via K+ transporters is essential for pollen tube growth; however, the mechanism by which K+ transporters are regulated in pollen tubes remains unknown. Here, we report that Arabidopsis thaliana Ca2+-dependent protein kinase11 (CPK11) and CPK24 are involved in Ca2+-dependent regulation of the inward K+ (K+in) channels in pollen tubes. Using patch-clamp analysis, we demonstrated that K+in currents of pollen tube protoplasts were inhibited by elevated [Ca2+]cyt. However, disruption of CPK11 or CPK24 completely impaired the Ca2+-dependent inhibition of K+in currents and enhanced pollen tube growth. Moreover, the cpk11 cpk24 double mutant exhibited similar phenotypes as the corresponding single mutants, suggesting that these two CDPKs function in the same signaling pathway. Bimolecular fluorescence complementation and coimmunoprecipitation experiments showed that CPK11 could interact with CPK24 in vivo. Furthermore, CPK11 phosphorylated the N terminus of CPK24 in vitro, suggesting that these two CDPKs work together as part of a kinase cascade. Electrophysiological assays demonstrated that the Shaker pollen K+in channel is the main contributor to pollen tube K+in currents and acts as the downstream target of the CPK11-CPK24 pathway. We conclude that CPK11 and CPK24 together mediate the Ca2+-dependent inhibition of K+in channels and participate in the regulation of pollen tube growth in Arabidopsis.
机译:钾(K + )通过K + 转运蛋白流入花粉管对于花粉管的生长至关重要。然而,在花粉管中调控K + 转运蛋白的机制尚不清楚。在这里,我们报道拟南芥Ca 2 + 依赖性蛋白激酶11(CPK11)和CPK24参与Ca 2 + 依赖性内向K +的调节花粉管中的(K + in )通道。通过膜片钳分析,我们证明了升高的[Ca 2 + ] 抑制了花粉管原生质体中的K + in 电流cyt 。但是,破坏CPK11或CPK24完全削弱了Ca 2 + 依赖的电流对K + 的抑制,并增强了花粉管的生长。此外,cpk11 cpk24双突变体表现出与相应的单个突变体相似的表型,表明这两个CDPK在相同的信号传导途径中起作用。双分子荧光互补和免疫共沉淀实验表明,CPK11可以在体内与CPK24相互作用。此外,CPK11在体外使CPK24的N末端磷酸化,表明这两个CDPK作为激酶级联的一部分共同发挥作用。电生理学分析表明,摇床中的摇床花粉K + 电流中花粉管K + 的主要贡献者。并充当CPK11-CPK24途径的下游目标。我们得出结论,CPK11和CPK24共同介导Ca2 + 依赖的K + 通道中的抑制作用,并参与花粉管生长的调控。拟南芥。

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