首页> 美国卫生研究院文献>Journal of Experimental Botany >Nitric oxide-activated calcium/calmodulin-dependent protein kinase regulates the abscisic acid-induced antioxidant defence in maize
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Nitric oxide-activated calcium/calmodulin-dependent protein kinase regulates the abscisic acid-induced antioxidant defence in maize

机译:一氧化氮激活的钙/钙调蛋白依赖性蛋白激酶调节玉米脱落酸诱导的抗氧化防御

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摘要

Nitric oxide (NO), hydrogen peroxide (H2O2), and calcium (Ca2+)/calmodulin (CaM) are all required for abscisic acid (ABA)-induced antioxidant defence. Ca2+/CaM-dependent protein kinase (CCaMK) is a strong candidate for the decoder of Ca2+ signals. However, whether CCaMK is involved in ABA-induced antioxidant defence is unknown. The results of the present study show that exogenous and endogenous ABA induced increases in the activity of ZmCCaMK and the expression of ZmCCaMK in leaves of maize. Subcellular localization analysis showed that ZmCCaMK is located in the nucleus, the cytoplasm, and the plasma membrane. The transient expression of ZmCCaMK and the RNA interference (RNAi) silencing of ZmCCaMK analysis in maize protoplasts revealed that ZmCCaMK is required for ABA-induced antioxidant defence. Moreover, treatment with the NO donor sodium nitroprusside (SNP) induced the activation of ZmCCaMK and the expression of ZmCCaMK. Pre-treatments with an NO scavenger and inhibitor blocked the ABA-induced increases in the activity and the transcript level of ZmCCaMK. Conversely, RNAi silencing of ZmCCaMK in maize protoplasts did not affect the ABA-induced NO production, which was further confirmed using a mutant of OsCCaMK, the homologous gene of ZmCCaMK in rice. Moreover, H2O2 was also required for the ABA activation of ZmCCaMK, and pre-treatments with an NO scavenger and inhibitor inhibited the H2O2-induced increase in the activity of ZmCCaMK. Taken together, the data clearly suggest that ZmCCaMK is required for ABA-induced antioxidant defence, and H2O2-dependent NO production plays an important role in the ABA-induced activation of ZmCCaMK.
机译:一氧化氮(NO),过氧化氢(H2O2)和钙(Ca 2 + )/钙调蛋白(CaM)都是脱落酸(ABA)诱导的抗氧化剂防御所必需的。 Ca 2 + / CaM依赖性蛋白激酶(CCaMK)是Ca 2 + 信号解码器的强大候选者。但是,CCaMK是否参与ABA诱导的抗氧化剂防御尚不清楚。本研究结果表明,外源和内源ABA诱导玉米叶片中ZmCCaMK的活性和ZmCCaMK的表达增加。亚细胞定位分析表明ZmCCaMK位于细胞核,细胞质和质膜中。玉米原生质体中ZmCCaMK的瞬时表达和ZmCCaMK分析的RNA干扰(RNAi)沉默表明,ZmCCaMK是ABA诱导的抗氧化剂防御所必需的。此外,用NO供体硝普钠(SNP)处理可诱导ZmCCaMK的活化和ZmCCaMK的表达。用NO清除剂和抑制剂进行的预处理可阻止ABA诱导的ZmCCaMK的活性和转录水平增加。相反,玉米原生质体中ZmCCaMK的RNAi沉默不影响ABA诱导的NO产生,这可以通过水稻中ZmCCaMK的同源基因OsCCaMK突变体进一步证实。此外,还需要H2O2来激活ZmCCaMK的ABA,用NO清除剂和抑制剂进行的预处理抑制了H2O2诱导的ZmCCaMK活性的增加。两者合计,数据清楚地表明ZmCCaMK是ABA诱导的抗氧化剂防御所必需的,并且H2O2依赖性NO的产生在ABA诱导的ZmCCaMK激活中起重要作用。

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