PIN2 is required for the adaptation of Arabidopsis roots to alkaline stress by modulating proton secretion

Journal of Experimental Botany

Volumn 63, Issue 17, 2012, Pages 6105-6114

  Xu, Weifeng ^a,b   Jia, Liguo ^c   ŠekBaluška, Franti ^d   Ding, Guochang ^c,e   Shi, Weiming ^b   Ye, Nenghui ^a   Zhang, Jianhua ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^c HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

^d UNIVERSITY OF BONN   (Germany)

^e FUJIAN AGRICULTURE AND FORESTRY UNIVERSITY   (China)

Author keywords

Alkaline stress; auxin transport; PIN2; PKS5; plasma membrane H + ATPase; primary root growth; proton secretion; root tip

Indexed keywords

ARABIDOPSIS PROTEIN; INDOLEACETIC ACID DERIVATIVE; PHYTOHORMONE; PIN2 PROTEIN, ARABIDOPSIS; PKS5 PROTEIN, ARABIDOPSIS; PROTEIN SERINE THREONINE KINASE; PROTON; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE;

ADAPTATION; ARABIDOPSIS; ARTICLE; CELL MEMBRANE; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; MUTATION; PH; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PLANT ROOT; SECRETION (PROCESS); SIGNAL TRANSDUCTION; TRANSPORT AT THE CELLULAR LEVEL;

ADAPTATION, PHYSIOLOGICAL; ARABIDOPSIS; ARABIDOPSIS PROTEINS; BIOLOGICAL TRANSPORT; CELL MEMBRANE; GENE EXPRESSION REGULATION, PLANT; HYDROGEN-ION CONCENTRATION; INDOLEACETIC ACIDS; MUTATION; PLANT GROWTH REGULATORS; PLANT ROOTS; PROTEIN-SERINE-THREONINE KINASES; PROTON-TRANSLOCATING ATPASES; PROTONS; SIGNAL TRANSDUCTION; STRESS, PHYSIOLOGICAL;

ARABIDOPSIS;

EID: 84868034838     PISSN: 00220957     EISSN: 14602431     Source Type: Journal    
DOI: 10.1093/jxb/ers259     Document Type: Article

References (34)

1. Baluška F, Mancuso S, Volkmann D, Barlow PW. 2010. Root apex transition zone: a signaling-response nexus in the root. Trends in Plant Science 15, 402-408.
2. Darwin CR (assisted by Darwin F). 1880. The power of movement in plants. John Murray (http://darwin-online.org.uk/).
3. Degenhardt B, Gimmler H, Hose E, Hartung W. 2000. Effect of alkaline and saline substrate on ABA content, distribution and transport in plant roots. Plant and Soil 225, 83-94.
4. Fu X, Harberd NP. 2003. Auxin promotes Arabidopsis root growth by modulating gibberellin response. Nature 421, 740-743.
5. Fuglsang AT, Guo Y, Cuin TA, et al. 2007. Arabidopsis protein kinase PKS5 inhibits the plasma membrane H+-ATPase by preventing interaction with 14-3-3 protein. The Plant Cell 19, 1617-1634.
6. Grieneisen VA, Xu J, Maree AFM, Hogeweg P, Scheres B. 2007. Auxin transport is sufficient to generate a maximum and gradient guiding root growth. Nature 449, 1008-1013.
7. Guo Y, Halfter U, Ishitani M, Zhu JK. 2001. Molecular characterization of functional domains in the protein kinase SOS2 that is required for plant salt tolerance. The Plant Cell 13, 731-740.
8. Hager A, Debus G, Edel HG, Stransky H, Serrano R. 1991. Auxin induces exocytosis and the rapid synthesis of a high-turnover pool of plasma-membrane H+-ATPase. Planta 185, 527-537.
9. Hager A. 2003. Role of the plasma membrane H+-ATPase in auxininduced elongation growth: historical and new aspects. Journal of Plant Research 116, 483-505.
10. Hurkman WJ. 1992. Effect of salt stress on plant gene expression: a review. Plant and Soil 146, 145-151.
11. Jin H, Plaha P, Park JY, et al. 2006. Comparative EST profiles of leaf and root of Leymus chinensis, a xerophilous grass adapted to high pH sodic soil. Plant Science 170, 1081-1086.
12. Kawanabe S, Zhu TC. 1991. Degeneration and conservation of Aneurolepisium chinense grassland in northern China. Journal of Japan Grassland Science 37, 91-99.
13. Kleine-Vehn J, Leitner J, Zwiewka M, Sauer M, Abas L, Luschnig C, Friml J. 2008. Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting. Proceedings of the National Academy of Sciences, USA 105, 17812-17817.
14. Lewis DR, Muday GK. 2001. Measurement of auxin transport in Arabidopsis thaliana. Nature Protocols 4, 437-451.
15. Li Q, Li BH, Kronzucker HJ, Shi WM. 2010. Root growth inhibition by NH4 + in Arabidopsis is mediated by the root tip and is linked to NH4 + efflux and GMPase activity. Plant, Cell and Environment 33, 1529-1542.
16. Liu J, Guo Y. 2011. The alkaline tolerance in Arabidopsis requires microfilament partially through inactivation of PKS5 kinase. Journal of Genetics and Genomics 38, 307-313.
17. Moloney MM, Elliott MC, Cleland RE. 1981. Acid growth effects in maize roots: evidence for a link between auxin-economy and proton extrusion in the control of root growth. Planta 152, 285-291.
18. Palmgren MG. 2001. Plant plasma membrane H+-ATPases: powerhouses for nutrient uptake. Annual Review of Plant Physiology and Plant Molecular Biology 52, 817-845.
19. Rober-Kleber N, Albrechtova JTP, Fleig S, Huck N, Michalke W, Wagner E, Speth V, Neuhaus G, Fischer-Iglesias C. 2003. Plasma membrane of H+-ATPases is involved in auxin-mediated cell elongation during wheat embryo development. Plant Physiology 131, 1302-1312.
20. Santi S, Schmidt W. 2009. Dissecting iron deficiency-induced proton extrusion in Arabidopsis root. New Phytologist 183, 1072-1084.
21. Schlicht M, Samajova O, Schachtschabel D, Mancuso S, Menzel D, Boland W, Baluška F. 2008. D'orenone blocks polarized tip growth of root hairs by interfering with the PIN2-mediated auxin transport network in the root apex. The Plant Journal 55, 709-717.
22. Shen H, Chen J, Wang Z, Yang C, Sasaki T, Yamamoto Y, Matsumoto H, Yan X. 2006. Root plasma membrane H+-ATPase activity is involved in the adaptation of soybean to phosphorus starvation. Journal of Experimental Botany 57, 1353-1362.
23. Shi D, Wang D. 2005. Effect of various salt-alkaline mixed stresses on Aneurolepidium chinense (Trin.) Kitag. Plant and Soil 271, 15-26.
24. Staal M, Cnodder TD, Simon D, Vandenbussche F, Straeten DVD, Verbelen JP, Elzenga T, Vissenberg K. 2011. Apoplastic alkalinization is instrumental for the inhibition of cell elongation in Arabidopsis root by the ethylene precursor 1-aminocyclopropane-1-carboxylic acid. Plant Physiology 155, 2049-2055.
25. Verbelen JP, Cnodder TD, Le J, Vissenberg K, Baluška F. 2006. The root apex of Arabidopsis thaliana consists of four distinct zones of growth activities. Plant Signaling and Behavior 1, 296-304.
26. Wang Y, Ma H, Liu G, Xu C, Zhang D, Ban Q. 2008. Analysis of gene expression profile of Limonium bicolor under NaHCO3 stress using cDNA microarray. Plant Molecular Biology Reporter 26, 241-254.
27. Xu WF, Shi WM. 2006. Expression profiling of the 14-3-3 gene family in response to salt stress and potassium and iron deficiencies in young tomato (Solanum lycopersicum) roots: analysis by real-time RT-PCR. Annals of Botany 98, 965-974.
28. Xu WF, Shi WM. 2007. Mechanisms of salt tolerance in transgenic Arabidopsis thaliana constitutively overexpressing the tomato 14-3-3 protein TFT7. Plant and Soil 301, 17-28.
29. Xu WF, Shi WM. 2008. A 'nonsterile' method for selecting and growing Arabidopsis thaliana transformants (T2 Transgenic Lines) resistant to kanamycin. Plant Molecular Biology Reporter 26, 350-357.
30. Xu WF, Shi WM, Jia LG, Liang JS, Zhang JH. 2012. TFT6 and TFT7, two different members of tomato 14-3-3 gene family, play distinct roles in plant adaption to low phosphorus stress. Plant, Cell and Environment 35, 1393-1406.
31. Yamaguchi M, Sharp RE. 2010. Complexity and coordination of root growth at low water potencials: recent advances from transcriptomic and proteomic analyses. Plant, Cell and Environment 33, 590-603.
32. Yang C, Wang P, Li C, Shi D, Wang D. 2008. Comparison of effect of salt and alkali stresses on the growth and photosynthesis of wheat. Photosynthetica 46, 107-114.
33. Yang Y, Qin Y, Xie C, et al. 2010. The Arabidopsis chaperone J3 regulates the plasma membrane H+-ATPase through interaction with the PKS5 kinase. The Plant Cell 22, 1313-1332.
34. Zhu JK. 2001. Plant salt tolerance. Trends in Plant Science 6, 66-71.