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首页> 外文期刊>Journal of Experimental Botany >Sucrose regulates wall ingrowth deposition in phloem parenchyma transfer cells in Arabidopsis via affecting phloem loading activity
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Sucrose regulates wall ingrowth deposition in phloem parenchyma transfer cells in Arabidopsis via affecting phloem loading activity

机译:蔗糖调节在拟南芥中验证薄膜膜转移细胞中的壁向沉积,通过影响韧皮血管素加载活性

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In Arabidopsis thaliana, phloem parenchyma transfer cells (PPTCs) occur in leaf minor veins and play a pivotal role in phloem loading. Wall ingrowth formation in PPTCs is induced by the phloem loading activity of these cells, which is regulated by sucrose (Suc). The effects of endogenous versus exogenous Suc on wall ingrowth deposition, however, differ. Elevating endogenous Suc levels by increased light enhanced wall ingrowth formation, whereas lowering endogenous Suc levels by dark treatment or genetically in ch-1 resulted in lower levels of deposition. In contrast, exogenously applied Suc, or Suc derived from other organs, repressed wall ingrowth deposition. Analysis of pAtSUC2::GFP plants, used as a marker for phloem loading status, suggested that wall ingrowth formation is correlated with phloem loading activity. Gene expression analysis revealed that exogenous Suc down-regulated expression of AtSWEET11 and 12, whereas endogenous Suc up-regulated AtSWEET11 expression. Analysis of a TREHALOSE 6-PHOSPHATE (T6P) SYNTHASE overexpression line and the hexokinase (HXK)-null mutant, gin2-1, suggested that Suc signalling of wall ingrowth formation is independent of T6P and HXK. Collectively, these results are consistent with the conclusion that Suc regulates wall ingrowth formation via affecting Suc exporting activity in PPTCs.
机译:在拟南芥中,Phloem Probyma转移细胞(PPTC)在叶片轻微静脉中发生,并在韧皮载荷中发挥枢轴作用。 PPTC中的壁环形成由这些细胞的韧皮植物负载活性诱导,其由蔗糖(SUC)调节。然而,内源性与外源性Suc对壁向沉积的影响不同。通过增加轻增强的壁环形成,提高内源性Suc水平,而通过暗处理或遗传在CH-1中降低内源性Suc水平,导致沉积水平较低。相比之下,外源应用Suc,或Suc衍生自其他器官,压抑的壁向沉积。 Patsuc2 :: GFP植物的分析用作韧皮植物负载状态的标志物,表明墙体向内形成与韧皮隆加载活性相关。基因表达分析表明,外源性Suc下调的ATSWeet11和12的表达,而内源性成功升高的ATSWeet11表达。对海藻糖6-磷酸(T6P)合成酶过表达线和六酮酶(HXK) - 纽尔突变体GIN2-1的分析表明,壁环形成的SUC信号与T6P和HXK无关。总的来说,这些结果与通过影响PPTC的Suc出口活性来调节壁向性形成的结论一致。

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