Institute of Biochemistry and Biophysics, Polish Academy of Sciences, ul. Pawińskiego 5a, 02-106, Poland.
J Biol Chem. 2011 Feb 4;286(5):3429-41. doi: 10.1074/jbc.M110.115535. Epub 2010 Nov 22.
SNF1-related protein kinases 2 (SnRK2s) are plant-specific enzymes involved in environmental stress signaling and abscisic acid-regulated plant development. Here, we report that SnRK2s interact with and are regulated by a plant-specific calcium-binding protein. We screened a Nicotiana plumbaginifolia Matchmaker cDNA library for proteins interacting with Nicotiana tabacum osmotic stress-activated protein kinase (NtOSAK), a member of the SnRK2 family. A putative EF-hand calcium-binding protein was identified as a molecular partner of NtOSAK. To determine whether the identified protein interacts only with NtOSAK or with other SnRK2s as well, we studied the interaction of an Arabidopsis thaliana orthologue of the calcium-binding protein with selected Arabidopsis SnRK2s using a two-hybrid system. All kinases studied interacted with the protein. The interactions were confirmed by bimolecular fluorescence complementation assay, indicating that the binding occurs in planta, exclusively in the cytoplasm. Calcium binding properties of the protein were analyzed by fluorescence spectroscopy using Tb(3+) as a spectroscopic probe. The calcium binding constant, determined by the protein fluorescence titration, was 2.5 ± 0.9 × 10(5) M(-1). The CD spectrum indicated that the secondary structure of the protein changes significantly in the presence of calcium, suggesting its possible function as a calcium sensor in plant cells. In vitro studies revealed that the activity of SnRK2 kinases analyzed is inhibited in a calcium-dependent manner by the identified calcium sensor, which we named SCS (SnRK2-interacting calcium sensor). Our results suggest that SCS is involved in response to abscisic acid during seed germination most probably by negative regulation of SnRK2s activity.
SNF1 相关蛋白激酶 2(SnRK2s)是参与环境胁迫信号转导和脱落酸调节植物发育的植物特异性酶。在这里,我们报告 SnRK2s 与植物特异性钙结合蛋白相互作用并受其调控。我们筛选了 Nicotiana plumbaginifolia Matchmaker cDNA 文库,以寻找与烟草渗透胁迫激活蛋白激酶(NtOSAK)相互作用的蛋白,NtOSAK 是 SnRK2 家族的成员。鉴定出一种假定的 EF 手钙结合蛋白是 NtOSAK 的分子伴侣。为了确定鉴定出的蛋白是否仅与 NtOSAK 相互作用还是与其他 SnRK2s 相互作用,我们使用双杂交系统研究了钙结合蛋白的拟南芥同源物与选定的拟南芥 SnRK2s 的相互作用。研究的所有激酶都与该蛋白相互作用。双分子荧光互补测定法证实了相互作用,表明结合发生在植物体内,仅在细胞质中发生。使用 Tb(3+)作为光谱探针通过荧光光谱分析了该蛋白的钙结合特性。通过蛋白荧光滴定法确定的钙结合常数为 2.5±0.9×10(5)M(-1)。CD 谱表明,在存在钙的情况下,该蛋白的二级结构发生显著变化,这表明其可能在植物细胞中作为钙传感器发挥作用。体外研究表明,所分析的 SnRK2 激酶的活性以钙依赖性方式被鉴定出的钙传感器抑制,我们将其命名为 SCS(SnRK2 相互作用的钙传感器)。我们的结果表明,SCS 可能通过负调控 SnRK2s 的活性参与种子萌发过程中对脱落酸的反应。