Expression of the cation transporter McHKT1 in a halophyte

被引:98
作者
Su, H
Balderas, E
Vera-Estrella, R
Golldack, D
Quigley, F
Zhao, CS
Pantoja, O
Bohnert, JH [1 ]
机构
[1] Univ Arizona, Dept Plant Sci, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Biochem, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[4] Univ Nacl Autonoma Mexico, Inst Biotechnol, Dept Biol Mol Plantas, Cuernavaca 62191, Morelos, Mexico
[5] Univ Bielefeld, Lehrstuhl Stoffwechselphysiol & Biochem Pflanzen, D-4800 Bielefeld, Germany
[6] Univ Grenoble 1, CNRS, UMR 5575, Lab Genet Mol Plantes, Grenoble, France
[7] Univ Illinois, ERML 196, Dept Plant Biol, Urbana, IL 61801 USA
[8] Univ Illinois, ERML 196, Dept Crop Sci, Urbana, IL 61801 USA
关键词
gene expression; halophyte; HKT1 cation transporter; Mesembryanthemum crystallinum; protein localization; sodium transport;
D O I
10.1023/A:1025445612244
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
From the ice plant, Mesembryanthemum crystallinum, McHKT1 was isolated encoding a protein 41-61% identical to other plant HKT1-like sequences previously described as potassium or sodium/potassium transporters. McHKT1 acts as a potassium transporter in yeast with specificity similar to that of wheat HKT1. In Xenopus oocytes it transports cations with a specificity Rb+>Cs+>[K+=Na+=Li+]. McHKT1 is exclusively localized to the plasma membrane. The isoform isolated is most highly expressed in leaves and is present in stems, flowers and seed pods but absent from the root where, according to immunological data, a second isoform exists which does not cross-hybridize with the leaf form in RNA blots at high stringency. McHKT1 transcript amounts increase during the first 6-10 h of stress and then decline to pre-stress levels with kinetics reminiscent of the initial influx of sodium into this halophyte. Immunocytological localization showed strong signals in the leaf vasculature and surrounding mesophyll cells but low-intensity signals are also detected in other cell types. In roots, McHKT is mainly confined to endodermis and stele. Possible functions of McHKT1 in ion homeostasis in the halophytic ice plant are discussed.
引用
收藏
页码:967 / 980
页数:14
相关论文
共 54 条
  • [1] ADAMS P, 1992, PLANT CELL PHYSIOL, V33, P1215
  • [2] Growth and development of Mesembryanthemum crystallinum (Aizoaceae)
    Adams, P
    Nelson, DE
    Yamada, S
    Chmara, W
    Jensen, RG
    Bohnert, HJ
    Griffiths, H
    [J]. NEW PHYTOLOGIST, 1998, 138 (02) : 171 - 190
  • [3] Amtmann A, 1999, ADV BOT RES, V29, P75
  • [4] Salt tolerance conferred by overexpression of a vacuolar Na+/H+ antiport in Arabidopsis
    Apse, MP
    Aharon, GS
    Snedden, WA
    Blumwald, E
    [J]. SCIENCE, 1999, 285 (5431) : 1256 - 1258
  • [5] Na+/H+ exchange in the halophyte Mesembryanthemum crystallinum is associated with cellular sites of Na+ storage
    Barkla, BJ
    Vera-Estrella, R
    Camacho-Emiterio, J
    Pantoja, O
    [J]. FUNCTIONAL PLANT BIOLOGY, 2002, 29 (09) : 1017 - 1024
  • [6] Functional analysis of AtHKT1 in Arabidopsis shows that Na+ recirculation by the phloem is crucial for salt tolerance
    Berthomieu, P
    Conéjéro, G
    Nublat, A
    Brackenbury, WJ
    Lambert, C
    Savio, C
    Uozumi, N
    Oiki, S
    Yamada, K
    Cellier, F
    Gosti, F
    Simonneau, T
    Essah, PA
    Tester, M
    Véry, AA
    Sentenac, H
    Casse, F
    [J]. EMBO JOURNAL, 2003, 22 (09) : 2004 - 2014
  • [7] Sodium transport in plant cells
    Blumwald, E
    Aharon, GS
    Apse, MP
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1465 (1-2): : 140 - 151
  • [8] Na+/myo-inositol symporters and Na+/H+-antiport in Mesembryanthemum crystallinum
    Chauhan, S
    Forsthoefel, N
    Ran, YQ
    Quigley, F
    Nelson, DE
    Bohnert, HJ
    [J]. PLANT JOURNAL, 2000, 24 (04) : 511 - 522
  • [9] Demidchik V, 2002, PLANT PHYSIOL, V128, P379, DOI 10.1104/pp.010524
  • [10] Site directed mutagenesis reduces the Na+ affinity of HKT1, an Na+ energized high affinity K+ transporter
    Diatloff, E
    Kumar, R
    Schachtman, DP
    [J]. FEBS LETTERS, 1998, 432 (1-2) : 31 - 36