Łabuz Justyna, Samardakiewicz Sławomir, Hermanowicz Paweł, Wyroba Elżbieta, Pilarska Maria, Gabryś Halina
Department of Plant Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland.
Laboratory of Electron and Confocal Microscopy, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.
J Exp Bot. 2016 Jun;67(13):3953-64. doi: 10.1093/jxb/erw089. Epub 2016 Mar 8.
Calcium is involved in the signal transduction pathway from phototropins, the blue light photoreceptor kinases which mediate chloroplast movements. The chloroplast accumulation response in low light is controlled by both phot1 and phot2, while only phot2 is involved in avoidance movement induced by strong light. Phototropins elevate cytosolic Ca(2+) after activation by blue light. In higher plants, both types of chloroplast responses depend on Ca(2+), and internal calcium stores seem to be crucial for these processes. Yet, the calcium signatures generated after the perception of blue light by phototropins are not well understood. To characterize the localization of calcium in Arabidopsis mesophyll cells, loosely bound (exchangeable) Ca(2+) was precipitated with potassium pyroantimonate and analyzed by transmission electron microscopy followed by energy-dispersive X-ray microanalysis. In dark-adapted wild-type Arabidopsis leaves, calcium precipitates were observed at the cell wall, where they formed spherical structures. After strong blue light irradiation, calcium at the apoplast prevailed, and bigger, multilayer precipitates were found. Spherical calcium precipitates were also detected at the tonoplast. After red light treatment as a control, the precipitates at the cell wall were smaller and less numerous. In the phot2 and phot1phot2 mutants, calcium patterns were different from those of wild-type plants. In both mutants, no elevation of calcium after blue light treatment was observed at the cell periphery (including the cell wall and a fragment of cytoplasm). This result confirms the involvement of phototropin2 in the regulation of Ca(2+) homeostasis in mesophyll cells.
钙参与了从向光素介导的信号转导途径,向光素是介导叶绿体运动的蓝光光受体激酶。弱光下的叶绿体积累反应受光1和光2共同控制,而强光诱导的回避运动仅涉及光2。蓝光激活后,向光素会提高胞质Ca(2+)浓度。在高等植物中,这两种类型的叶绿体反应都依赖于Ca(2+),并且内部钙库似乎对这些过程至关重要。然而,向光素感知蓝光后产生的钙信号仍未得到充分了解。为了表征拟南芥叶肉细胞中钙的定位,用焦锑酸钾沉淀松散结合(可交换)的Ca(2+),然后通过透射电子显微镜和能量色散X射线微分析进行分析。在暗适应的野生型拟南芥叶片中,在细胞壁处观察到钙沉淀,它们形成球形结构。强光蓝光照射后,质外体中的钙占主导,并且发现了更大的多层沉淀。在液泡膜处也检测到球形钙沉淀。作为对照,红光处理后,细胞壁处的沉淀较小且数量较少。在光2和光1光2突变体中,钙模式与野生型植物不同。在这两种突变体中,蓝光处理后在细胞周边(包括细胞壁和一部分细胞质)均未观察到钙浓度升高。这一结果证实了向光素2参与叶肉细胞中Ca(2+)稳态的调节。