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A RING-type E3 ligase controls anther dehiscence by activating the jasmonate biosynthetic pathway gene DEFECTIVE IN ANTHER DEHISCENCE1 in Arabidopsis

机译:a RING-type E3 ligase controls anther dehiscence by activating the jasmonate biosynthetic pathway gene DEFECTIVE IN aNTHER DEHIsCENCE1 in arabidopsis

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摘要

Suppression of expression of DAF [DEFECTIVE IN ANTHER DEHISCENCE1 (DAD1)-Activating Factor], a gene that encodes a putative RING-finger E3 ligase protein, causes non-dehiscence of the anthers, alters pollen development and causes sterility in 35S:DAF RNAi/antisense Arabidopsis plants. This mutant phenotype correlates with the suppression of DAF but not with expression of the two most closely related genes, DAFL1/2. The expression of DAD1 was significantly reduced in 35S:DAF RNAi/antisense plants, and complementation with 35S:DAF did not rescue the dad1 mutant, indicating that DAF acts upstream of DAD1 in jasmonic acid biosynthesis. This assumption is supported by the finding that 35S:DAF RNAi/antisense plants showed a similar cellular basis for anther dehiscence to that found in dad1 mutants, and that external application of jasmonic acid rescued the anther non-dehiscence and pollen defects in 35S:DAF antisense flowers. We further demonstrate that DAF is an E3 ubiquitin ligase and that its activity is abolished by C132S and H137Y mutations in its RING motif. Furthermore, ectopic expression of the dominant-negative C132S or H137Y mutations causes similar indehiscence of anthers and reduction in DAD1 expression in transgenic Arabidopsis. This result not only confirms that DAF controls anther dehiscence by positively regulating the expression of DAD1 in the jasmonic acid biosynthesis pathway, but also supports the notion that DAF functions as an E3 ubiquitin ligase, and that the conserved RING-finger region is required for its activity.
机译:DAF表达的抑制[花药抗性1(DAD1)激活因子],该基因编码假定的RING-手指E3连接酶蛋白,引起花药不裂开,改变花粉发育并导致35S:DAF RNAi不育/反义拟南芥植物。该突变表型与DAF的抑制有关,但与两个最密切相关的基因DAFL1 / 2的表达无关。 DAD1的表达在35S:DAF RNAi /反义植物中显着降低,与35S:DAF的互补不能挽救dad1突变体,表明DAF在茉莉酸生物合成中作用于DAD1的上游。 35S:DAF RNAi /反义植物显示出与dad1突变体相似的花药开裂的细胞基础,并且茉莉酸的外部应用挽救了35S:DAF的花药不开裂和花粉缺陷,这一假设得到了以下假设的支持。反义花。我们进一步证明DAF是一种E3泛素连接酶,并且其活性被RING主题中的C132S和H137Y突变所废除。此外,显性阴性C132S或H137Y突变的异位表达导致类似的花药开裂和转基因拟南芥中DAD1表达的降低。该结果不仅证实DAF通过积极调节茉莉酸生物合成途径中DAD1的表达来控制花药开裂,而且还支持DAF充当E3泛素连接酶的观点,并且其保守的RING-手指区域是必需的活动。

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