State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou 730070, China.
South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524091, China.
Int J Mol Sci. 2022 Aug 8;23(15):8795. doi: 10.3390/ijms23158795.
Calcium-dependent protein kinases (CDPK) are implicated in signaling transduction in eukaryotic organisms. It is largely unknown whether plays a role in the response to water deficiency and osmotic stress in potato plants ( L.). Potato cv. Zihuabai was cultivated under natural, moderate, and severe water deficiency conditions; to induce osmotic stress, potato plants were treated with 10% or 20% PEG. -overexpression and -knockdown plants were constructed. were evaluated by qRT-PCR. The subcellular location of the StCDPK28 protein was observed with confocal scanning laser microscopy. Phenotypic changes were indicated by photosynthetic activity, the contents of HO, MDA and proline, and the activities of CAT, SOD and POD. Results showed water deficiency and osmotic stress altered expression patterns. StCDPK28 exhibited a membrane, cytosolic and nuclear localization. Water deficiency and osmotic stress induced upregulation. Photosynthetic activity was enhanced by overexpression, while decreased by knockdown under water deficiency and osmotic stress. overexpression decreased HO and MDA, and increased proline, while knockdown showed reverse results, compared with the wild type, in response to water deficiency and osmotic stress. overexpression increased the activities of CAT, SOD and POD, while -knockdown plants indicated the reverse trend under water deficiency and osmotic stress conditions. Regulation of StCDPK28 expression could be a promising approach to improve the tolerance ability of potato plants in response to drought or high salt media.
钙依赖蛋白激酶(CDPK)参与真核生物信号转导。目前还不清楚在马铃薯(L.)对水分亏缺和渗透胁迫的响应中是否起作用。马铃薯 cv. 紫花白在自然、中度和重度水分亏缺条件下进行栽培;为了诱导渗透胁迫,用 10%或 20% PEG 处理马铃薯植株。构建了 -过表达和 -敲低植株。通过 qRT-PCR 评估 。用共聚焦扫描激光显微镜观察 StCDPK28 蛋白的亚细胞定位。通过光合活性、HO、MDA 和脯氨酸含量以及 CAT、SOD 和 POD 的活性来指示表型变化。结果表明,水分亏缺和渗透胁迫改变了 的表达模式。StCDPK28 表现出膜、胞质和核定位。水分亏缺和渗透胁迫诱导 上调。在水分亏缺和渗透胁迫下, -过表达增强了光合活性,而 -敲低则降低了光合活性。与野生型相比, -过表达在水分亏缺和渗透胁迫下降低了 HO 和 MDA,增加了脯氨酸,而 -敲低则表现出相反的结果。-过表达增加了 CAT、SOD 和 POD 的活性,而在水分亏缺和渗透胁迫条件下, -敲低植物则表现出相反的趋势。调节 StCDPK28 的表达可能是提高马铃薯植株对干旱或高盐介质的耐受能力的一种有前途的方法。