Dasgupta Kasturi, Khadilkar Aswad S, Sulpice Ronan, Pant Bikram, Scheible Wolf-Rüdiger, Fisahn Joachim, Stitt Mark, Ayre Brian G
Department of Biological Sciences, University of North Texas, Denton, Texas 76203 (K.D., A.S.K., B.G.A.);Max Planck Institute of Molecular Plant Physiology, D-14476 Potsdam-Golm, Germany (R.S., J.F., M.S.); andThe Samuel Roberts Noble Foundation, Plant Biology Division, Ardmore, Oklahoma 73401 (B.P., W.-R.S.).
Department of Biological Sciences, University of North Texas, Denton, Texas 76203 (K.D., A.S.K., B.G.A.);Max Planck Institute of Molecular Plant Physiology, D-14476 Potsdam-Golm, Germany (R.S., J.F., M.S.); andThe Samuel Roberts Noble Foundation, Plant Biology Division, Ardmore, Oklahoma 73401 (B.P., W.-R.S.)
Plant Physiol. 2014 Jun;165(2):715-731. doi: 10.1104/pp.114.238410. Epub 2014 Apr 28.
Sucrose (Suc) is the predominant form of carbon transported through the phloem from source to sink organs and is also a prominent sugar for short-distance transport. In all streptophytes analyzed, Suc transporter genes (SUTs or SUCs) form small families, with different subgroups evolving distinct functions. To gain insight into their capacity for moving Suc in planta, representative members of each clade were first expressed specifically in companion cells of Arabidopsis (Arabidopsis thaliana) and tested for their ability to rescue the phloem-loading defect caused by the Suc transporter mutation, Atsuc2-4. Sequence similarity was a poor indicator of ability: Several genes with high homology to AtSUC2, some of which have phloem-loading functions in other eudicot species, did not rescue the Atsuc2-4 mutation, whereas a more distantly related gene, ZmSUT1 from the monocot Zea mays, did restore phloem loading. Transporter complementary DNAs were also expressed in the companion cells of wild-type Arabidopsis, with the aim of increasing productivity by enhancing Suc transport to growing sink organs and reducing Suc-mediated feedback inhibition on photosynthesis. Although enhanced Suc loading and long-distance transport was achieved, growth was diminished. This growth inhibition was accompanied by increased expression of phosphate (P) starvation-induced genes and was reversed by providing a higher supply of external P. These experiments suggest that efforts to increase productivity by enhancing sugar transport may disrupt the carbon-to-P homeostasis. A model for how the plant perceives and responds to changes in the carbon-to-P balance is presented.
蔗糖(Suc)是通过韧皮部从源器官运输到库器官的主要碳形式,也是短距离运输的主要糖类。在所有已分析的链形植物中,蔗糖转运蛋白基因(SUTs或SUCs)形成小家族,不同亚组具有不同的功能。为了深入了解它们在植物中运输蔗糖的能力,首先在拟南芥(Arabidopsis thaliana)的伴胞中特异性表达每个进化枝的代表性成员,并测试它们挽救由蔗糖转运蛋白突变Atsuc2-4引起的韧皮部装载缺陷的能力。序列相似性并不能很好地指示能力:几个与AtSUC2具有高度同源性的基因,其中一些在其他双子叶植物物种中具有韧皮部装载功能,但不能挽救Atsuc2-4突变,而来自单子叶植物玉米的一个亲缘关系较远的基因ZmSUT1却能恢复韧皮部装载。转运蛋白互补DNA也在野生型拟南芥的伴胞中表达,目的是通过增强蔗糖向生长中的库器官的运输以及减少蔗糖介导的对光合作用的反馈抑制来提高生产力。虽然实现了增强的蔗糖装载和长距离运输,但生长却受到了抑制。这种生长抑制伴随着磷(P)饥饿诱导基因表达的增加,并且通过提供更高的外部磷供应而得以逆转。这些实验表明,通过增强糖运输来提高生产力的努力可能会破坏碳与磷的稳态。本文提出了一个植物如何感知和响应碳磷平衡变化的模型。