Bostock R M, Quatrano R S
Department of Plant Pathology, University of California, Davis, California 95616.
Plant Physiol. 1992 Apr;98(4):1356-63. doi: 10.1104/pp.98.4.1356.
Expression of the Em gene was characterized in rice (Oryza sativa L.) suspension cultures following exposure of the cultures to various combinations of abscisic acid (ABA) and salt. Response-saturating concentrations of either ABA (50 micromolar) or NaCl (0.4 molar) rapidly induced (by 60 minutes) the accumulation of Em mRNA, with a maximum accumulation occurring 12 to 24 hours after treatment. NaCl-induced Em expression was accompanied by a doubling of endogenous ABA levels as determined by immunoassay. Inhibition of ABA biosynthesis by fluridone during NaCl treatment reduced the levels of endogenous ABA by fourfold and Em expression by 50%. Desiccation of the cultures to 12 to 15% of their initial fresh weight increased endogenous ABA more than twofold and was accompanied by an increase in Em mRNA levels. Exposure of the cultures to heat shock temperatures, chilling, or ultraviolet light neither increased endogenous ABA levels nor induced Em expression. When a subthreshold or saturating level of NaCl was added in combination with increasing levels of ABA, Em transcripts were detected at ABA concentrations that alone did not induce expression of Em. Treatment with saturating levels of both NaCl and ABA resulted in a doubling of Em transcript levels over the maximum signal for each treatment alone. Hence, our data suggested that salt interacted synergistically with ABA, in part because of the increased sensitivity of rice cells to ABA. The effect of salt stress on Em gene expression in rice suspension cells appeared to operate through two pathways: one is mediated through increases in the level of ABA; the other is via a unique salt response pathway that includes an intermediate that is common to both the salt and ABA response chains.
在水稻(Oryza sativa L.)悬浮培养物中,将其暴露于脱落酸(ABA)和盐的各种组合后,对Em基因的表达进行了表征。ABA(50微摩尔)或NaCl(0.4摩尔)的响应饱和浓度迅速诱导(60分钟内)Em mRNA的积累,处理后12至24小时积累量达到最大。通过免疫测定确定,NaCl诱导的Em表达伴随着内源ABA水平的加倍。在NaCl处理期间,氟啶酮抑制ABA生物合成使内源ABA水平降低了四倍,Em表达降低了50%。将培养物干燥至其初始鲜重的12%至15%,使内源ABA增加了两倍多,并伴随着Em mRNA水平的增加。将培养物暴露于热激温度、低温或紫外线下,既不会增加内源ABA水平,也不会诱导Em表达。当添加低于阈值或饱和水平的NaCl与增加水平的ABA组合时,在单独不会诱导Em表达的ABA浓度下检测到Em转录本。用饱和水平的NaCl和ABA处理导致Em转录本水平比单独每种处理的最大信号增加了一倍。因此,我们的数据表明盐与ABA协同作用,部分原因是水稻细胞对ABA的敏感性增加。盐胁迫对水稻悬浮细胞中Em基因表达的影响似乎通过两条途径起作用:一条是通过ABA水平的增加介导的;另一条是通过独特的盐响应途径,该途径包括盐和ABA响应链共有的一种中间体。