College of Life Sciences, Nanjing Agricultural University, Nanjing, China.
J Exp Bot. 2013 Feb;64(4):871-84. doi: 10.1093/jxb/ers366. Epub 2012 Dec 26.
Calcium-dependent protein kinases (CDPKs) have been shown to be involved in abscisic acid (ABA)-mediated physiological processes, including seed germination, post-germination growth, stomatal movement, and plant stress tolerance. However, it is not clear whether CDPKs are involved in ABA-induced antioxidant defence. In the present study, the role of the maize CDPK ZmCPK11 in ABA-induced antioxidant defence and the relationship between ZmCPK11 and ZmMPK5, a maize ABA-activated mitogen-activated protein kinase (MAPK), in ABA signalling were investigated. Treatments with ABA and H(2)O(2) induced the expression of ZmCPK11 and increased the activity of ZmCPK11, while H(2)O(2) was required for the ABA-induced increases in the expression and the activity of ZmCPK11. The transient gene expression analysis and the transient RNA interference (RNAi) test in protoplasts showed that ZmCPK11 is involved in ABA-induced up-regulation of the expression and the activities of superoxide dismutase (SOD) and ascorbate peroxidase (APX), and in the production of H(2)O(2). Further, ZmCPK11 was shown to be required for the up-regulation of the expression and the activity of ZmMPK5 in ABA signalling, but ZmMPK5 had very little effect on the ABA-induced up-regulation of the expression and the activity of ZmCPK11. Moreover, the transient gene expression analysis in combination with the transient RNAi test in protoplasts showed that ZmCPK11 acts upstream of ZmMPK5 to regulate the activities of antioxidant enzymes. These results indicate that ZmCPK11 is involved in ABA-induced antioxidant defence and functions upstream of ZmMPK5 in ABA signalling in maize.
钙依赖型蛋白激酶(CDPKs)已被证明参与脱落酸(ABA)介导的生理过程,包括种子萌发、萌发后生长、气孔运动和植物应激耐受。然而,目前尚不清楚 CDPKs 是否参与 ABA 诱导的抗氧化防御。本研究探讨了玉米 CDPK ZmCPK11 在 ABA 诱导的抗氧化防御中的作用,以及 ZmCPK11 与玉米 ABA 激活的丝裂原活化蛋白激酶(MAPK)ZmMPK5 之间在 ABA 信号转导中的关系。ABA 和 H₂O₂处理诱导 ZmCPK11 的表达,并增加 ZmCPK11 的活性,而 H₂O₂是 ABA 诱导 ZmCPK11 表达和活性增加所必需的。原生质体中的瞬时基因表达分析和瞬时 RNA 干扰(RNAi)试验表明,ZmCPK11 参与 ABA 诱导的超氧化物歧化酶(SOD)和抗坏血酸过氧化物酶(APX)的表达和活性的上调,以及 H₂O₂的产生。此外,ZmCPK11 被证明是 ABA 信号转导中 ZmMPK5 表达和活性上调所必需的,但 ZmMPK5 对 ABA 诱导的 ZmCPK11 表达和活性上调几乎没有影响。此外,原生质体中的瞬时基因表达分析与瞬时 RNAi 试验相结合表明,ZmCPK11 在调节抗氧化酶活性方面位于 ZmMPK5 的上游。这些结果表明,ZmCPK11 参与 ABA 诱导的抗氧化防御,并在玉米 ABA 信号转导中位于 ZmMPK5 的上游。