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本文引用的文献

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Nitrate, nitrite and ammonia assimilation by leaves: Effect of light, carbon dioxide and oxygen.硝酸盐、亚硝酸盐和氨在叶片中的同化:光、二氧化碳和氧的影响。
Planta. 1974 Sep;116(3):207-24. doi: 10.1007/BF00390228.
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Nitrate efflux at the root plasma membrane: identification of an Arabidopsis excretion transporter.根质膜上的硝酸盐外流:一种拟南芥排泄转运蛋白的鉴定。
Plant Cell. 2007 Nov;19(11):3760-77. doi: 10.1105/tpc.106.048173. Epub 2007 Nov 9.
3
Nitrate transporters and peptide transporters.硝酸盐转运蛋白和肽转运蛋白。
FEBS Lett. 2007 May 25;581(12):2290-300. doi: 10.1016/j.febslet.2007.04.047. Epub 2007 Apr 26.
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The FRD3-mediated efflux of citrate into the root vasculature is necessary for efficient iron translocation.FRD3介导的柠檬酸外流进入根脉管系统对于有效的铁转运是必要的。
Plant Physiol. 2007 May;144(1):197-205. doi: 10.1104/pp.107.097162. Epub 2007 Mar 9.
5
The Arabidopsis NRT1.1 transporter participates in the signaling pathway triggering root colonization of nitrate-rich patches.拟南芥NRT1.1转运蛋白参与触发根系定殖于富硝酸盐斑块的信号通路。
Proc Natl Acad Sci U S A. 2006 Dec 12;103(50):19206-11. doi: 10.1073/pnas.0605275103. Epub 2006 Dec 5.
6
Dissection of the AtNRT2.1:AtNRT2.2 inducible high-affinity nitrate transporter gene cluster.拟南芥NRT2.1:NRT2.2诱导型高亲和力硝酸盐转运蛋白基因簇的剖析
Plant Physiol. 2007 Jan;143(1):425-33. doi: 10.1104/pp.106.091223. Epub 2006 Nov 3.
7
Studies of the Uptake of Nitrate in Barley : IV. Electrophysiology.大麦硝酸盐吸收的研究:IV. 电生理学。
Plant Physiol. 1992 Jun;99(2):456-63. doi: 10.1104/pp.99.2.456.
8
Mutant of Arabidopsis deficient in xylem loading of phosphate.拟南芥中缺乏磷酸盐木质部装载的突变体。
Plant Physiol. 1991 Nov;97(3):1087-93. doi: 10.1104/pp.97.3.1087.
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Cell type-specific expression profiling in plants via cell sorting of protoplasts from fluorescent reporter lines.通过对荧光报告株系原生质体进行细胞分选来分析植物中细胞类型特异性的表达谱。
Nat Methods. 2005 Aug;2(8):615-9. doi: 10.1038/nmeth0805-615.
10
The putative high-affinity nitrate transporter NRT2.1 represses lateral root initiation in response to nutritional cues.假定的高亲和力硝酸盐转运蛋白NRT2.1会根据营养信号抑制侧根起始。
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拟南芥NRT1.5硝酸盐转运蛋白的突变导致根部到地上部的硝酸盐转运缺陷。

Mutation of the Arabidopsis NRT1.5 nitrate transporter causes defective root-to-shoot nitrate transport.

作者信息

Lin Shan-Hua, Kuo Hui-Fen, Canivenc Geneviève, Lin Choun-Sea, Lepetit Marc, Hsu Po-Kai, Tillard Pascal, Lin Huey-Ling, Wang Ya-Yun, Tsai Chyn-Bey, Gojon Alain, Tsay Yi-Fang

机构信息

Institute of Molecular Biology, Academia Sinica, Taipei 11529, Taiwan.

出版信息

Plant Cell. 2008 Sep;20(9):2514-28. doi: 10.1105/tpc.108.060244. Epub 2008 Sep 9.

DOI:10.1105/tpc.108.060244
PMID:18780802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2570733/
Abstract

Little is known about the molecular and regulatory mechanisms of long-distance nitrate transport in higher plants. NRT1.5 is one of the 53 Arabidopsis thaliana nitrate transporter NRT1 (Peptide Transporter PTR) genes, of which two members, NRT1.1 (CHL1 for Chlorate resistant 1) and NRT1.2, have been shown to be involved in nitrate uptake. Functional analysis of cRNA-injected Xenopus laevis oocytes showed that NRT1.5 is a low-affinity, pH-dependent bidirectional nitrate transporter. Subcellular localization in plant protoplasts and in planta promoter-beta-glucuronidase analysis, as well as in situ hybridization, showed that NRT1.5 is located in the plasma membrane and is expressed in root pericycle cells close to the xylem. Knockdown or knockout mutations of NRT1.5 reduced the amount of nitrate transported from the root to the shoot, suggesting that NRT1.5 participates in root xylem loading of nitrate. However, root-to-shoot nitrate transport was not completely eliminated in the NRT1.5 knockout mutant, and reduction of NRT1.5 in the nrt1.1 background did not affect root-to-shoot nitrate transport. These data suggest that, in addition to that involving NRT1.5, another mechanism is responsible for xylem loading of nitrate. Further analyses of the nrt1.5 mutants revealed a regulatory loop between nitrate and potassium at the xylem transport step.

摘要

关于高等植物中长距离硝酸盐运输的分子和调控机制,人们了解甚少。NRT1.5是拟南芥53个硝酸盐转运蛋白NRT1(肽转运蛋白PTR)基因之一,其中两个成员NRT1.1(耐氯酸盐1的CHL1)和NRT1.2已被证明参与硝酸盐吸收。对注射cRNA的非洲爪蟾卵母细胞的功能分析表明,NRT1.5是一种低亲和力、pH依赖的双向硝酸盐转运蛋白。在植物原生质体中的亚细胞定位、在植物中的启动子-β-葡萄糖醛酸酶分析以及原位杂交表明,NRT1.5位于质膜上,并在靠近木质部的根中柱鞘细胞中表达。NRT1.5的敲低或敲除突变减少了从根向地上部运输的硝酸盐量,这表明NRT1.5参与了根木质部对硝酸盐的装载。然而,在NRT1.5敲除突变体中,根到地上部的硝酸盐运输并未完全消除,并且在nrt1.1背景中NRT1.5的减少并不影响根到地上部的硝酸盐运输。这些数据表明,除了涉及NRT1.5的机制外,另一种机制负责木质部对硝酸盐的装载。对nrt1.5突变体的进一步分析揭示了在木质部运输步骤中硝酸盐和钾之间的调控环。