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乙烯生物合成对水稻幼苗抗稻瘟病菌感染的作用。

Contribution of ethylene biosynthesis for resistance to blast fungus infection in young rice plants.

作者信息

Iwai Takayoshi, Miyasaka Atsushi, Seo Shigemi, Ohashi Yuko

机构信息

National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Plant Physiol. 2006 Nov;142(3):1202-15. doi: 10.1104/pp.106.085258. Epub 2006 Sep 29.

Abstract

The role of ethylene (ET) in resistance to infection with blast fungus (Magnaporthe grisea) in rice (Oryza sativa) is poorly understood. To study it, we quantified ET levels after inoculation, using young rice plants at the four-leaf stage of rice cv Nipponbare (wild type) and its isogenic plant (IL7), which contains the Pi-i resistance gene to blast fungus race 003. Small necrotic lesions by hypersensitive reaction (HR) were formed at 42 to 72 h postinoculation (hpi) in resistant IL7 leaves, and whitish expanding lesions at 96 hpi in susceptible wild-type leaves. Notable was the enhanced ET emission at 48 hpi accompanied by increased 1-aminocyclopropane-1-carboxylic acid (ACC) levels and highly elevated ACC oxidase (ACO) activity in IL7 leaves, whereas only an enhanced ACC increase at 96 hpi in wild-type leaves. Among six ACC synthase (ACS) and seven ACO genes found in the rice genome, OsACS2 was transiently expressed at 48 hpi in IL7 and at 96 hpi in wild type, and OsACO7 was expressed at 48 hpi in IL7. Treatment with an inhibitor for ACS, aminooxyacetic acid, suppressed enhanced ET emission at 48 hpi in IL7, resulting in expanding lesions instead of HR lesions. Exogenously supplied ACC compromised the aminooxyacetic acid-induced breakdown of resistance in IL7, and treatment with 1-methylcyclopropene and silver thiosulfate, inhibitors of ET action, did not suppress resistance. These findings suggest the importance of ET biosynthesis and, consequently, the coproduct, cyanide, for HR-accompanied resistance to blast fungus in young rice plants and the contribution of induced OsACS2 and OsACO7 gene expression to it.

摘要

乙烯(ET)在水稻(Oryza sativa)对稻瘟病菌(Magnaporthe grisea)感染的抗性中所起的作用尚不清楚。为了对此进行研究,我们在接种后对ET水平进行了定量分析,使用的是水稻品种日本晴(野生型)及其同基因植株(IL7)处于四叶期的幼苗,IL7含有对稻瘟病菌003小种的Pi-i抗性基因。接种后42至72小时(hpi),抗性IL7叶片通过过敏反应(HR)形成小坏死斑,而在96 hpi时,感病野生型叶片出现白色扩展病斑。值得注意的是,IL7叶片在48 hpi时ET释放增强,同时1-氨基环丙烷-1-羧酸(ACC)水平升高,ACC氧化酶(ACO)活性大幅提高,而野生型叶片仅在96 hpi时ACC增加增强。在水稻基因组中发现的6个ACC合酶(ACS)基因和7个ACO基因中,OsACS2在IL7中于48 hpi时短暂表达,在野生型中于96 hpi时短暂表达,而OsACO7在IL7中于48 hpi时表达。用ACS抑制剂氨基氧乙酸处理可抑制IL7在48 hpi时增强的ET释放,导致形成扩展病斑而非HR病斑。外源供应ACC可减轻氨基氧乙酸诱导的IL7抗性丧失,而用ET作用抑制剂1-甲基环丙烯和硫代硫酸银处理并未抑制抗性。这些发现表明ET生物合成以及其副产物氰化物对于水稻幼苗中伴随HR的稻瘟病菌抗性的重要性,以及诱导的OsACS2和OsACO7基因表达对其的贡献。

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