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Phosphate availability regulates ethylene biosynthesis gene expression and protein accumulation in white clover (Trifolium repens L.) roots

机译:磷酸盐的可用性调节白三叶草(Trifolium repens L.)根中乙烯的生物合成基因表达和蛋白质积累

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摘要

The expression and accumulation of members of the 1-aminocyclopropane-1-carboxylate (ACC) synthase (ACS) and ACC oxidase (ACO) gene families was examined in white clover roots grown in either Pi (phosphate) sufficient or Pi-deprived defined media. The accumulation of one ACO isoform, TR-ACO1, was positively influenced after only 1 h of exposure to low Pi, and this was maintained over a 7-day time-course. Up-regulation of TR-ACS1, TR-ACS2 and TR-ACS3 transcript abundance was also observed within 1 h of exposure to low Pi in different tissue regions of the roots, followed by a second increase in abundance of TR-ACS2 after 5–7 days of exposure. An increase in transcript abundance of TR-ACO1 and TR-ACO3, but not TR-ACO2, was observed after 1 h of exposure to low Pi, with a second increase in TR-ACO1 transcripts occurring after 2–5 days. These initial increases of the TR-ACS and TR-ACO transcript abundance occurred before the induction of Trifolium repens PHOSPHATE TRANSPORTER 1 (TR-PT1), and the addition of sodium phosphite did not up-regulate TR-ACS1 expression over 24 h. In situ hybridization revealed some overlap of TR-ACO mRNA accumulation, with TR-ACO1 and TR-ACO2 in the root tip regions, and TR-ACO1 and TR-ACO3 mRNA predominantly in the lateral root primordia. TR-ACO1p-driven GFP expression showed that activation of the TR-ACO1 promoter was initiated within 24 h of exposure to low Pi (as determined by GFP protein accumulation). These results suggest that the regulation of ethylene biosynthesis in white clover roots is biphasic in response to low Pi supply.
机译:在生长于Pi(磷酸盐)充足或Pi缺乏的特定培养基中的三叶草根中检查了1-氨基环丙烷-1-甲酸(ACC)合酶(ACS)和ACC氧化酶(ACO)基因家族成员的表达和积累。仅在暴露于低Pi下1小时后,一种ACO异构体TR-ACO1的积累受到了积极影响,并且在7天的时间范围内保持这种状态。在根部不同组织区域暴露于低Pi后1小时内,还观察到TR-ACS1,TR-ACS2和TR-ACS3转录物的丰度上调,然后在5–5分钟后第二次TR-ACS2的丰度增加暴露7天。暴露于低Pi下1小时后,观察到TR-ACO1和TR-ACO3的转录本丰度增加,而TR-ACO2则没有,而2-5天后TR-ACO1转录本又增加了一次。 TR-ACS和TR-ACO转录物丰度的这些最初增加发生在白三叶草磷酸盐转运蛋白1(TR-PT1)的诱导之前,亚磷酸钠的添加在24小时内并未上调TR-ACS1表达。原位杂交显示TR-ACO mRNA积累有一些重叠,在根尖区域有TR-ACO1和TR-ACO2,而在侧根原基中主要有TR-ACO1和 TR-ACO3 mRNA。 TR-ACO1p 驱动的GFP表达表明 TR-ACO1 启动子的激活在暴露于低Pi的24小时内启动(由GFP蛋白积累确定)。这些结果表明白三叶草根中乙烯生物合成的调节是双相的,以响应低磷供应。

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