Agrawal Ganesh K, Rakwal Randeep, Iwahashi Hitoshi
Research Laboratory for Agricultural Biotechnology and Biochemistry (RLABB), GPO Box 8207, Kathmandu, Nepal.
Biochem Biophys Res Commun. 2002 Jun 28;294(5):1009-16. doi: 10.1016/S0006-291X(02)00571-5.
In search for components of MAPK (mitogen-activated protein kinase) cascades in rice (Oryza sativa L. cv. Nipponbare), we identified a single copy gene called OsMSRMK2 from jasmonic acid (JA) treated rice seedling leaf cDNA library. This gene has a conserved protein kinase domain, including a MAPK family signature, and encodes a 369 amino acid polypeptide with a predicted molecular mass of 42995.43 and a pI of 5.48. OsMSRMK2 did not show constitutive expression in leaves and was induced within 15 min in response to wounding by cut. Using in vitro system, we show that the expression of OsMSRMK2 mRNA was potently enhanced within 15 min by signalling molecules, protein phosphatase inhibitors, ultraviolet irradiation, fungal elicitor, heavy metals, high salt and sucrose, and drought. OsMSRMK2 expression was further modulated by co-application of JA, salicylic acid, and ethylene and required de novo synthesized protein factor(s) in its transient regulation. Moreover, high (37 degrees C) and low temperatures (12 degrees C) and environmental pollutants-ozone and sulfur dioxide-differentially regulate the OsMSRMK2 mRNA accumulation in leaves of intact plants. Present results demonstrating dramatic transcriptional and transient regulation of the OsMSRMK2 expression by diverse biotic/abiotic stresses, a first report for any rice (or plant) MAPK to date, suggest a role for OsMSRMK2 in rice defense/stress response pathways.
为了寻找水稻(日本晴)中促分裂原活化蛋白激酶(MAPK)级联反应的组分,我们从茉莉酸(JA)处理的水稻幼苗叶片cDNA文库中鉴定出一个单拷贝基因,命名为OsMSRMK2。该基因具有一个保守的蛋白激酶结构域,包括一个MAPK家族特征序列,编码一个369个氨基酸的多肽,预测分子量为42995.43,等电点为5.48。OsMSRMK2在叶片中不呈组成型表达,在切割伤口处理后15分钟内被诱导表达。利用体外系统,我们发现信号分子、蛋白磷酸酶抑制剂、紫外线照射、真菌激发子、重金属、高盐、蔗糖和干旱在15分钟内可显著增强OsMSRMK2 mRNA的表达。JA、水杨酸和乙烯共同作用可进一步调节OsMSRMK2的表达,且其瞬时调节需要从头合成的蛋白质因子。此外,高温(37℃)和低温(12℃)以及环境污染物——臭氧和二氧化硫——对完整植株叶片中OsMSRMK2 mRNA的积累有不同的调节作用。目前的结果表明,多种生物/非生物胁迫可对OsMSRMK2的表达进行显著的转录和瞬时调节,这是迄今为止关于任何水稻(或植物)MAPK的首次报道,提示OsMSRMK2在水稻防御/胁迫反应途径中发挥作用。