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. 1995 Nov;109(3):735–742. doi: 10.1104/pp.109.3.735

Ion Homeostasis in NaCl Stress Environments.

X Niu 1, R A Bressan 1, P M Hasegawa 1, J M Pardo 1
PMCID: PMC161372  PMID: 12228628

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Selected References

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  1. Anderson J. A., Huprikar S. S., Kochian L. V., Lucas W. J., Gaber R. F. Functional expression of a probable Arabidopsis thaliana potassium channel in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1992 May 1;89(9):3736–3740. doi: 10.1073/pnas.89.9.3736. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Banta L. M., Robinson J. S., Klionsky D. J., Emr S. D. Organelle assembly in yeast: characterization of yeast mutants defective in vacuolar biogenesis and protein sorting. J Cell Biol. 1988 Oct;107(4):1369–1383. doi: 10.1083/jcb.107.4.1369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barkla B. J., Blumwald E. Identification of a 170-kDa protein associated with the vacuolar Na+/H+ antiport of Beta vulgaris. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11177–11181. doi: 10.1073/pnas.88.24.11177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berkelman T., Houtchens K. A., DuPont F. M. Two cDNA clones encoding isoforms of the B subunit of the vacuolar ATPase from barley roots. Plant Physiol. 1994 Jan;104(1):287–288. doi: 10.1104/pp.104.1.287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Binzel M. L., Hess F. D., Bressan R. A., Hasegawa P. M. Intracellular compartmentation of ions in salt adapted tobacco cells. Plant Physiol. 1988 Feb;86(2):607–614. doi: 10.1104/pp.86.2.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boutry M., Michelet B., Goffeau A. Molecular cloning of a family of plant genes encoding a protein homologous to plasma membrane H+-translocating ATPases. Biochem Biophys Res Commun. 1989 Jul 31;162(2):567–574. doi: 10.1016/0006-291x(89)92348-6. [DOI] [PubMed] [Google Scholar]
  7. Braun Y., Hassidim M., Lerner H. R., Reinhold L. Studies on H-Translocating ATPases in Plants of Varying Resistance to Salinity : I. Salinity during Growth Modulates the Proton Pump in the Halophyte Atriplex nummularia. Plant Physiol. 1986 Aug;81(4):1050–1056. doi: 10.1104/pp.81.4.1050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cosgrove D. J., Hedrich R. Stretch-activated chloride, potassium, and calcium channels coexisting in plasma membranes of guard cells of Vicia faba L. Planta. 1991 Dec;186(1):143–153. doi: 10.1007/BF00201510. [DOI] [PubMed] [Google Scholar]
  9. Ewing N. N., Wimmers L. E., Meyer D. J., Chetelat R. T., Bennett A. B. Molecular Cloning of Tomato Plasma Membrane H-ATPase. Plant Physiol. 1990 Dec;94(4):1874–1881. doi: 10.1104/pp.94.4.1874. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fernando M., Mehroke J., Glass A. D. De Novo Synthesis of Plasma Membrane and Tonoplast Polypeptides of Barley Roots during Short-Term K Deprivation : In Search of the High-Affinity K Transport System. Plant Physiol. 1992 Nov;100(3):1269–1276. doi: 10.1104/pp.100.3.1269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gaber R. F., Styles C. A., Fink G. R. TRK1 encodes a plasma membrane protein required for high-affinity potassium transport in Saccharomyces cerevisiae. Mol Cell Biol. 1988 Jul;8(7):2848–2859. doi: 10.1128/mcb.8.7.2848. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gaxiola R., de Larrinoa I. F., Villalba J. M., Serrano R. A novel and conserved salt-induced protein is an important determinant of salt tolerance in yeast. EMBO J. 1992 Sep;11(9):3157–3164. doi: 10.1002/j.1460-2075.1992.tb05392.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Haro R., Garciadeblas B., Rodríguez-Navarro A. A novel P-type ATPase from yeast involved in sodium transport. FEBS Lett. 1991 Oct 21;291(2):189–191. doi: 10.1016/0014-5793(91)81280-l. [DOI] [PubMed] [Google Scholar]
  14. Jia Z. P., McCullough N., Martel R., Hemmingsen S., Young P. G. Gene amplification at a locus encoding a putative Na+/H+ antiporter confers sodium and lithium tolerance in fission yeast. EMBO J. 1992 Apr;11(4):1631–1640. doi: 10.1002/j.1460-2075.1992.tb05209.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Katz A., Bental M., Degani H., Avron M. In Vivo pH Regulation by a Na/H Antiporter in the Halotolerant Alga Dunaliella salina. Plant Physiol. 1991 May;96(1):110–115. doi: 10.1104/pp.96.1.110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Katz A., Pick U., Avron M. Modulation of Na/H Antiporter Activity by Extreme pH and Salt in the Halotolerant Alga Dunaliella salina. Plant Physiol. 1992 Nov;100(3):1224–1229. doi: 10.1104/pp.100.3.1224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Latterich M., Watson M. D. Isolation and characterization of osmosensitive vacuolar mutants of Saccharomyces cerevisiae. Mol Microbiol. 1991 Oct;5(10):2417–2426. doi: 10.1111/j.1365-2958.1991.tb02087.x. [DOI] [PubMed] [Google Scholar]
  18. Mendoza I., Rubio F., Rodriguez-Navarro A., Pardo J. M. The protein phosphatase calcineurin is essential for NaCl tolerance of Saccharomyces cerevisiae. J Biol Chem. 1994 Mar 25;269(12):8792–8796. [PubMed] [Google Scholar]
  19. Michelet B., Boutry M. The Plasma Membrane H+-ATPase (A Highly Regulated Enzyme with Multiple Physiological Functions). Plant Physiol. 1995 May;108(1):1–6. doi: 10.1104/pp.108.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Müller-Röber B., Ellenberg J., Provart N., Willmitzer L., Busch H., Becker D., Dietrich P., Hoth S., Hedrich R. Cloning and electrophysiological analysis of KST1, an inward rectifying K+ channel expressed in potato guard cells. EMBO J. 1995 Jun 1;14(11):2409–2416. doi: 10.1002/j.1460-2075.1995.tb07238.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Narasimhan M. L., Binzel M. L., Perez-Prat E., Chen Z., Nelson D. E., Singh N. K., Bressan R. A., Hasegawa P. M. NaCl Regulation of Tonoplast ATPase 70-Kilodalton Subunit mRNA in Tobacco Cells. Plant Physiol. 1991 Oct;97(2):562–568. doi: 10.1104/pp.97.2.562. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Niu X., Zhu J. K., Narasimhan M. L., Bressan R. A., Hasegawa P. M. Plasma-membrane H(+)-ATPase gene expression is regulated by NaCl in cells of the halophyte Atriplex nummularia L. Planta. 1993;190(4):433–438. doi: 10.1007/BF00224780. [DOI] [PubMed] [Google Scholar]
  23. Perez-Prat E., Narasimhan M. L., Binzel M. L., Botella M. A., Chen Z., Valpuesta V., Bressan R. A., Hasegawa P. M. Induction of a Putative Ca-ATPase mRNA in NaCl-Adapted Cells. Plant Physiol. 1992 Nov;100(3):1471–1478. doi: 10.1104/pp.100.3.1471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Plant P. J., Gelli A., Blumwald E. Vacuolar chloride regulation of an anion-selective tonoplast channel. J Membr Biol. 1994 May;140(1):1–12. doi: 10.1007/BF00234481. [DOI] [PubMed] [Google Scholar]
  25. Rains D. W., Epstein E. Sodium absorption by barley roots: its mediation by mechanism 2 of alkali cation transport. Plant Physiol. 1967 Mar;42(3):319–323. doi: 10.1104/pp.42.3.319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Sarafian V., Kim Y., Poole R. J., Rea P. A. Molecular cloning and sequence of cDNA encoding the pyrophosphate-energized vacuolar membrane proton pump of Arabidopsis thaliana. Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1775–1779. doi: 10.1073/pnas.89.5.1775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Schachtman D. P., Schroeder J. I. Structure and transport mechanism of a high-affinity potassium uptake transporter from higher plants. Nature. 1994 Aug 25;370(6491):655–658. doi: 10.1038/370655a0. [DOI] [PubMed] [Google Scholar]
  28. Schachtman D. P., Tyerman S. D., Terry B. R. The k/na selectivity of a cation channel in the plasma membrane of root cells does not differ in salt-tolerant and salt-sensitive wheat species. Plant Physiol. 1991 Oct;97(2):598–605. doi: 10.1104/pp.97.2.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Schnapp S. R., Curtis W. R., Bressan R. A., Hasegawa P. M. Growth Yields and Maintenance Coefficients of Unadapted and NaCl-Adapted Tobacco Cells Grown in Semicontinuous Culture. Plant Physiol. 1991 Aug;96(4):1289–1293. doi: 10.1104/pp.96.4.1289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Schroeder J. I., Ward J. M., Gassmann W. Perspectives on the physiology and structure of inward-rectifying K+ channels in higher plants: biophysical implications for K+ uptake. Annu Rev Biophys Biomol Struct. 1994;23:441–471. doi: 10.1146/annurev.bb.23.060194.002301. [DOI] [PubMed] [Google Scholar]
  31. Sentenac H., Bonneaud N., Minet M., Lacroute F., Salmon J. M., Gaymard F., Grignon C. Cloning and expression in yeast of a plant potassium ion transport system. Science. 1992 May 1;256(5057):663–665. doi: 10.1126/science.1585180. [DOI] [PubMed] [Google Scholar]
  32. Sussman M. R., Harper J. F. Molecular biology of the plasma membrane of higher plants. Plant Cell. 1989 Oct;1(10):953–960. doi: 10.1105/tpc.1.10.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wada M., Takano M., Kasamo K. Nucleotide Sequence of a Complementary DNA Encoding Plasma Membrane H-ATPase from Rice (Oryza sativa L.). Plant Physiol. 1992 Jun;99(2):794–795. doi: 10.1104/pp.99.2.794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wan C. Y., Wilkins T. A. Isolation of multiple cDNAs encoding the vacuolar H(+)-ATPase subunit B from developing cotton (Gossypium hirsutum L.) ovules. Plant Physiol. 1994 Sep;106(1):393–394. doi: 10.1104/pp.106.1.393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wimmers L. E., Ewing N. N., Bennett A. B. Higher plant Ca(2+)-ATPase: primary structure and regulation of mRNA abundance by salt. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9205–9209. doi: 10.1073/pnas.89.19.9205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Zimniak L., Dittrich P., Gogarten J. P., Kibak H., Taiz L. The cDNA sequence of the 69-kDa subunit of the carrot vacuolar H+-ATPase. Homology to the beta-chain of F0F1-ATPases. J Biol Chem. 1988 Jul 5;263(19):9102–9112. [PubMed] [Google Scholar]

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