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首页> 外文期刊>The New Phytologist >Eliminating the purple acid phosphatase AtPAP26 in Arabidopsis thaliana delays leaf senescence and impairs phosphorus remobilization
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Eliminating the purple acid phosphatase AtPAP26 in Arabidopsis thaliana delays leaf senescence and impairs phosphorus remobilization

机译:消除拟南芥中的紫色酸性磷酸酶AtPAP26会延迟叶片衰老并损害磷的固定

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摘要

Limitation of crop productivity by suboptimal phosphorus (P) nutrition is a widespread concern. Enhanced crop P-use efficiency could be achieved by improving P remobilization from senescing leaves to developing tissues and seeds. Transcriptomic studies indicate that hundreds of Arabidopsis thaliana genes are up-regulated during leaf senescence, including that encoding the purple acid phosphatase (PAP) AtPAP26 (At5g34850). In this study, biochemical and functional genomic tools were integrated to testthe hypothesis that AtPAP26 participates in P remobilization during leaf senescence. An eightfold increase in acid phosphatase activity of senescing leaves was correlated with the accumulation of AIPAP26 transcripts and immunoreactive AtPAP26 polypeptides. Senescing leaves of an atpap26 T-DNA insertion mutant displayed a > 90% decrease in acid phosphatase activity, markedly impaired P remobilization efficiency and delayed senescence. This was paralleled by reduced seed total P concentrations and germination rates. These results demonstrate that AtPAP26 loss of function causes dramatic effects that cannot be compensated for by any other PAP isozyme, even though Arabidopsis contains 29 different PAP genes. Our current and earlier studies establish thatAtPAP26 not only helps to scavenge P from organic P sources when Arabidopsis is cultivated in inorganic orthophosphate (Pi)-deficient soils, but also has an important P remobilization function during leaf senescence.
机译:欠佳的磷(P)营养限制了农作物的生产力,这是引起广泛关注的问题。通过改善磷从衰老叶片向发育中的组织和种子的迁移,可以提高作物磷的利用效率。转录组学研究表明,数百个拟南芥基因在叶片衰老过程中被上调,其中包括编码紫色酸性磷酸酶(PAP)AtPAP26(At5g34850)的基因。在这项研究中,整合了生物化学和功能基因组学工具,以检验AtPAP26参与叶片衰老过程中P迁移的假说。衰老叶片酸性磷酸酶活性的八倍增加与AIPAP26转录本和免疫反应性AtPAP26多肽的积累有关。 atpap26 T-DNA插入突变体的感性叶片显示酸性磷酸酶活性降低> 90%,显着削弱P的固定效率并延缓衰老。同时降低种子的总磷浓度和发芽率。这些结果表明,即使拟南芥含有29个不同的PAP基因,AtPAP26功能丧失也会引起无法用任何其他PAP同工酶补偿的戏剧性影响。我们当前和较早的研究表明,在拟南芥种植于无机正磷酸盐(Pi)缺乏的土壤中时,AtPAP26不仅有助于从有机磷源中清除磷,而且在叶片衰老过程中也具有重要的磷转运功能。

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