Institute of Plant Biology and Biotechnology, University of Münster, 48143 Muenster, Germany.
Plant Cell. 2011 Aug;23(8):2950-63. doi: 10.1105/tpc.111.087973. Epub 2011 Aug 19.
The plant-specific calcium binding protein CAS (calcium sensor) has been localized in chloroplast thylakoid membranes of vascular plants and green algae. To elucidate the function of CAS in Chlamydomonas reinhardtii, we generated and analyzed eight independent CAS knockdown C. reinhardtii lines (cas-kd). Upon transfer to high-light (HL) growth conditions, cas-kd lines were unable to properly induce the expression of LHCSR3 protein that is crucial for nonphotochemical quenching. Prolonged exposure to HL revealed a severe light sensitivity of cas-kd lines and caused diminished activity and recovery of photosystem II (PSII). Remarkably, the induction of LHCSR3, the growth of cas-kd lines under HL, and the performance of PSII were fully rescued by increasing the calcium concentration in the growth media. Moreover, perturbing cellular Ca(2+) homeostasis by application of the calmodulin antagonist W7 or the G-protein activator mastoparan impaired the induction of LHCSR3 expression in a concentration-dependent manner. Our findings demonstrate that CAS and Ca(2+) are critically involved in the regulation of the HL response and particularly in the control of LHCSR3 expression.
植物特异性钙结合蛋白 CAS(钙传感器)已被定位在维管束植物和绿藻的叶绿体类囊体膜中。为了阐明 CAS 在莱茵衣藻中的功能,我们生成并分析了八个独立的 CAS 敲低莱茵衣藻系(cas-kd)。在转移到高光(HL)生长条件下,cas-kd 系无法正确诱导对非光化学猝灭至关重要的 LHCSR3 蛋白的表达。长时间暴露于 HL 会导致 cas-kd 系严重的光敏感性,并导致 PSII 活性和恢复能力下降。值得注意的是,通过增加生长介质中的钙浓度,可以完全挽救 LHCSR3 的诱导、cas-kd 系在 HL 下的生长以及 PSII 的性能。此外,通过应用钙调蛋白拮抗剂 W7 或 G 蛋白激活剂 mastoparan 扰乱细胞内 Ca(2+)稳态,以浓度依赖的方式损害 LHCSR3 表达的诱导。我们的研究结果表明,CAS 和 Ca(2+)在 HL 反应的调节中,特别是在 LHCSR3 表达的控制中起着至关重要的作用。