Acta Agron Sin ›› 2015, Vol. 41 ›› Issue (02): 259-275.doi: 10.3724/SP.J.1006.2015.00259
• TILLAGE & CULTIVATION · PHYSIOLOGY & BIOCHEMISTRY • Previous Articles Next Articles
YIN Gui-Xiang,ZHANG Lei*,SHE Mao-Yun
| [1]Wang Y, Wu W H. Plant sensing and signaling in response to K+-deficiency. Mol Plant, 2010, 3: 280–287[2]Ashley M K, Grant M, Grabov A. Plant responses to potassium deficiencies: a role for potassium transport proteins. J Exp Bot, 2006, 57: 425–436[3]Epstein E, Rains D W, Elzam O E. Resolution of dual mechanisms of potassium absorption by barley roots. Proc Natl Acad Sci USA, 1963, 49: 684–692[4]Fairbairn D J, Liu W, Schachtman D P, Gomez-Gallego S, Day S R, Teasdale R D. Characterization of two distinct HKT1-like potassium transporters from Eucalyptus camaldulensis. Plant Mol Biol, 2000, 43: 515–525[5]Uozumi N, Kim E J, Rubio F, Yamaguchi T, Muto S, Tsuboi A, Bakker E P, Nakamura T, Schroeder J I. The Arabidopsis HKT1 gene homolog mediates inward Na+ currents in Xenopus laevis oocytes and Na+ uptake in Saccharomyces cerevisiae. Plant Physiol, 2000, 122: 1249–1259[6]Berthomieu P, Conéjéro G, Nublat A, Brackenbury W J, Lambert C, Savio C, Uozumi N, Oiki S, Yamada K, Cellier F, Gosti F, Simonneau T, Essah P A, Tester M, Véry A A, Sentenac H, Casse F. Functional analysis of AtHKT1 in Arabidopsis shows that Na+ recirculation by the phloem is crucial for salt tolerance. EMBO J, 2003, 22: 2004–2014[7]Rubio F, Schwarz M, Gassmann W, Schroeder J I. Genetic selection of mutations in the high affinity K+ transporter HKT1 that define functions of a loop site for reduced Na+ permeability and increased Na+ tolerance. J Biol Chem, 1999, 274: 6839–6847[8]Ren Z H, Gao J P, Li L G, Cai X L, Huang W, Chao D Y, Zhu M Z, Wang Z Y, Luan S, Lin H X. A rice quantitative trait locus for salt tolerance encodes a sodium transporter. Nature Gen, 2005, 37: 1141–1146[9]Wang T B, Gassmann W, Rubio F, Schroeder J I, Glass D M. Rapid up-regulation of HKT1, a high-affinity potassium transporter gene, in roots of barley and wheat following withdrawal of potassium. Plant Physiol, 1998, 118: 651–659[10]Chen H, He H, Yu D. Overexpression of a novel soybean gene modulating Na+ and K+ transport enhances salt tolerance in transgenic tobacco plants. Physiol Plant, 2011, 141: 11–18[11]Chen H T, Chen X, Gu H P, Wu B Y, Zhang H M, Yuan X X, Cui X Y. GmHKT1;4, a novel soybean gene regulating Na+/K+ ratio in roots enhances salt tolerance in transgenic plants. Plant Growth Regul, 2014, 73: 299–308[12]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 USA, 1992, 89: 3736–3740[13]Schachtman D P, Schroeder J I. Structure and transport mechanism of a high-affinity potassium uptake transporter from higher plants. Nature, 1994, 370: 655–658[14]Gassmann W, Rubio F, Schroeder J I. Alkali cation selectivity of the wheat root high-affinity potassium transporter HKT1. Plant J, 1996, 10: 869–882[15]Rubio F, Gassmann W, Schroeder J I. Sodium-driven potassium uptake by the plant potassium transporter HKT1 and mutations conferring salt tolerance. Science, 1995, 270: 1660–1663[16]Aleman F, Nieves-Cordones M, Nieves-Cordones M, Martinez V, Rubio F. Root K(+) acquisition in plants: the Arabidopsis thaliana model. Plant Cell Physiol, 2011, 52: 1603–1612[17]Kato Y, Sakaguchi M, Mori Y, Saito K, Nakamura T, Bakker E P, Sato Y, Goshima S, Uozumi N. Evidence in support of a four transmembrane-pore-transmembrane topology model for the Arabidopsis thaliana Na+/K+ translocating AtHKT1 protein, a member of the superfamily of K+ transporters. Proc Natl Acad Sci USA, 2001, 98: 6488–6493[18]Durell S R, Hao Y, Nakamura T, Bakker E P, Guy H R. Evolutionary relationship between K+ channels and symporters. Biophys J, 1999, 77: 775–788[19]M?ser P, Hosoo Y, Goshima S, Horie T, Eckelman B, Yamada K, Yoshida K, Bakker E P, Shinmyo A, Oiki S, Schroeder J I, Uozumi N. Glycine residues in potassium channel-like selectivity filters determine potassium selectivity in four-loop-per-subunit HKT transporters from plants. Proc Natl Acad Sci USA, 2002, 99: 6428–6433[20]Wang Y, Wu W H. Potassium transport and signaling in higher plants. Annu Rev Plant Biol, 2013, 64: 451–476[21]Véry A A, Sentenac H. Molecular mechanisms and regulation of K+ transport in higher plants. Annu Rev Plant Biol, 2003, 54: 575–603[22]Waters S, Gilliham M, Hrmova M. Plant high-affinity potassium (HKT) transporters involved in salinity tolerance: structural insights to probe differences in ion selectivity. Int J Mol Sci, 2013, 14: 7660–7680[23]Kader M A, Lindberg S. Uptake of sodium in protoplasts of salt-sensitive and salt-tolerant cultivars of rice, Oryza sativa L. determined by the fluorescent dye SBFI. J Exp Bot, 2005, 56: 3149–3158[24]Tester M, Davenport R. Na+ tolerance and Na+ transport in higher plants. Ann Bot (Lond.), 2003, 91: 503–527[25]M?ser P, Eckelman B, Vaidyanathan R, Horie T, Fairbairn D J, Kubo M, Yamagami M, Yamaguchi K, Nishimura M, Uozumi N, Robertson W, Sussman M R, Schroeder J I. Altered shoot/root Na+ distribution and bifurcating salt sensitivity in Arabidopsis by genetic disruption ofthe Na+ transporter AtHKT1. FEBS Lett, 2002, 531: 157–161[26]Rus A, Lee B H, Mu?oz-Mayor A, Sharkhuu A, Miura K, Zhu J K, Bressan R A, Hasegawa PM. AtHKT1 facilitates Na+ homeostasis and K+ nutrition in planta. Plant Physiol, 2004, 136: 2500–2511[27]Sunarpi, Horie T, Motoda J, Kubo M, Yang H, Yoda K, Horie R, Chan W Y, Leung H Y, Hattori K, Konomi M, Osumi M, Yamagami M, Schroeder J I, Uozumi N. Enhanced salt tolerance mediated by AtHKT1 transporter-induced Na+ unloading from xylem parenchyma cells. Plant J, 2005, 44: 928–938[28]Horie T, Costa A, Kim T H, Han M J, Horie R, Leung H Y, Miyao A, Hirochika H, An G, Schroeder J I. Rice OsHKT2;1 transporter mediates large Na+ influx component into K+-starved roots for growth. EMBO J, 2007, 26: 3003–3014[29]Zhu J K, Liu J, Xiong L. Genetic analysis of salt tolerance in Arabidopsis: evidence for a critical role of potassium nutrition. Plant Cell, 1998, 10: 1181–1191[30]Alemán F, Nieves-Cordones M, Martínez V, Rubio F. Potassium/sodium steady-state homeostasis in Thellungiella halophila and Arabidopsis thaliana under long-term salinity conditions. Plant Sci, 2009, 176: 768–774[31]Zhu J K. Cell signaling under salt, water and cold stresses. Curr Opin Plant Biol, 2001, 4: 401–406[32]唐劲驰, 曹敏建, 祝子平, 闫洪奎, 刘绍鹏. 不同基因型大豆对低钾的耐性极限及缺钾症状研究简报. 大豆科学, 2001, 20: 295–297Tang J C, Cao M J, Zhu Z P, Yan H K, Liu S P. Resistence limit and symptom of different genotypes of soybean to low potassium. Soybean Sci, 2001, 20: 295–297 (in Chinese with English abstract)[33]权月伟, 李喜焕, 常文锁, 张彩英. 大豆耐低钾种质资源筛选研究. 华北农学报, 2011, 26(增刊): 51–55Quan Y W, Li X H, Chang W S, Zhang C Y. Screening of low potassium tolerant soybean (Glycine max) varieties from Hebei soybean-growing-areas. Acta Agric Boreali-Sin, 2011, 26 (suppl): 51–55 (in Chinese with English abstract)[34]王伟, 曹敏建, 綦左莹, 何萍, 许海涛. 不同大豆品种对钾素吸收和利用效率差异的比较研究. 大豆科学, 2007, 26: 561–564Wang W, Cao M J, Qi Z Y, He P, Xu H T. Comparison of potassium absorb and use efficiency in soybean (Glycine max L. Merr.) varieties. Soybean Sci, 2007, 26: 561–564 (in Chinese with English abstract)[35]Damien Platten J, Cotsaftis O, Berthomieu P, Bohnert H, Davenport R J, Fairbairn D J, Horie T, Leigh R A, Lin H X, Luan S, M?ser P, Pantoja O, Rodríguez-Navarro A, Schachtman D P, Schroeder J I, Sentenac H, Uozumi N, Véry A, Zhu J K, Dennis E S, Tester M. Nomenclature for HKT transporters, key determinants of plant salinity tolerance. Trends Plant Sci, 2006, 11: 372–374[36]Kato N, Akai M, Zulkifli L, Matsuda N, Kato Y, Goshima S, Hazama A, Yamagami M, Guy H R, Uozumi N. Role of positively charged amino acids in the M2(D) transmembrane helix of Ktr/Trk/HKT type cation transporters. Channels, 2007, 1: 161–171[37]Cao Y, Jin X, Huang H, Derebe M G, Levin E J, Kabaleeswaran V, Pan Y, Punta M, Love J, Weng J, Quick M, Ye S, Kloss B, Bruni R, Martinez-Hackert E, Hendrickson W A, Rost B, Javitch J A, Rajashankar K R, Jiang Y, Zhou M. Crystal structure of a potassium ion transporter, TrkH. Nature, 2011, 471: 336–340[38]Ardie S W, Xie L N, Takahashi R, Liu S K, Takano T. Cloning of a high-affinity K+ transporter gene PutHKT2;1 from Puccinellia tenuiflora and its functional comparison with OsHKT2;1 from rice in yeast and Arabidopsis. J Exp Bot, 2009, 60: 3491–3502[39]Munns R, James R A, Xu B, Athman A, Conn S J, Jordans C, Byrt C S, Hare R A, Tyerman S D, Tester M, Plett D, Gilliham M. Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene. Nature Biotech, 2012, 30: 360–366[40]Ali Z, Park H C, Ali A, Oh D H, Aman R, Kropornicka A, Hong H, Choi W, Chung W S, Kim W Y, Bressan R A, Bohnert H J, Lee S Y, Yun D J. TsHKT1;2, a HKT1 homolog from the extremophile Arabidopsis relative Thellungiella salsuginea, shows K+ specificity in the presence of NaCl. Plant Physiol, 2012, 158: 1463–1474[41]Asins M J, Villalta I, Aly M M, Olías R, álvarez De Morales P, Huertas R, Li J, Jaime-Pérez N, Haro R, Raga V, Carbonell E A, Belver A. Two closely linked tomato HKT coding genes are positional candidates for the major tomato QTL involved in Na+/K+ homeostasis. Plant Cell Environ, 2013, 36: 1171–1191[42]Almeida P, de Boer G J, de Boer A H. Differences in shoot Na+ accumulation between two tomato species are due to differences in ion affinity of HKT1;2. J Plant Physiol, 2014, 171: 438–447[43]Cotsaftis O, Plett D, Shirley N, Tester M, Hrmova M. A two-stage model of Na+ exclusion in rice explained by 3D modeling of HKT transporters and alternative splicing. PLoS One, 2012, 7: e39865[44]Lan W Z, Wang W, Wang S M, Li L G, Buchanan B B, Lin H X, Gao J P, Luan S. A rice high-affinity potassium transporter (HKT) conceals a calcium-permeable cation channel. Proc Natl Acad Sci USA, 2010, 107: 7089–7094[45]Koltunow A M, Truettner J, Cox K H, Wallroth M, Goldberg R. Different temporal and spatial gene expression patterns occur during anther development. Plant Cell, 1990, 2: 1201–1224[46]Schauer A, Ranes M, Santamaria R, Guijarro J, Lawlor E, Mendez C, Chater K, Losick R. Visualizing gene expression in time and space in the filamentous bacterium Streptomyces coelicolor. Science, 1988, 240: 768–772[47]McGuire S E, Roman G, Davis R L. Gene expression systems in Drosophila: a synthesis of time and space. Trends Genet, 2004, 20: 384–391[48]Liang P, Acerboukh L, Pardee A B. Distribution and cloning of eukarytic mRNAs by means of differential display: refinements and optimization. Nucl Acids Res, 1993, 21: 3269–3275 |
| [1] | Tang Kuan-Qiang, Li Gong-Yun, Song Mei-Yi, Zhao Xue, Chang Chun-Ling. Genome-wide association analysis and prediction model construction for soybean plant height [J]. Acta Agronomica Sinica, 2026, 52(6): 1743-1756. |
| [2] | Yao Shu, Guo Kai-Yue, Zhai Hui-Hui, Yao Jia-Hui, Deng Wen-Qi, Yan Ling, Huang Chi, Gao Yang, Yu Yan-Ran, Zhao Zhen-Bang, Li Ying-Hui, Wang Xiao-Bo, Li Jia-Jia. Comprehensive evaluation of low-iron tolerance and screening of elite germplasm at the soybean seedling stage [J]. Acta Agronomica Sinica, 2026, 52(5): 1373-1387. |
| [3] | Zhang Qing, Yang Yu, Guo Qian, Yue Pei-Yao, Yin Cong-Cong, Niu Jing-Ping, Zhao Jin-Zhong, Du Wei-Jun, Yue Ai-Qin. Cloning and functional analysis of the soybean GmARA6a gene in response to salt stress [J]. Acta Agronomica Sinica, 2026, 52(2): 480-493. |
| [4] | Yang Biao, Du Shuai-Kang, Zhang Ji-Wang, Shi Ying, Zhang Li-Li. Genome-wide identification of class III POD gene family in potato and its expression profile analysis [J]. Acta Agronomica Sinica, 2026, 52(2): 405-420. |
| [5] | Jing Xiu-Qing, Cai Yong-Duo, Deng Ning, Zhao Xiao-Dong, Zhai Fei-Hong, Zeng Qun. Identification and expression pattern analysis of RopGEF family genes in Chenopodium quinoa [J]. Acta Agronomica Sinica, 2026, 52(1): 28-43. |
| [6] | WANG Ke-Jing, LI Xiang-Hua. Endangerment assessment of the perennial species G. tabacina and G. tomentella of the genus Glycine Willd. in China [J]. Acta Agronomica Sinica, 2025, 51(8): 2009-2019. |
| [7] | MENG Ran, LI Zhao-Jia, FENG Wei, CHEN Yue, LIU Lu-Ping, YANG Chun-Yan, LU Xue-Lin, WANG Xiu-Ping. Comprehensive evaluation of salt tolerance at different growth stages of soybean and screening of salt-tolerant germplasm [J]. Acta Agronomica Sinica, 2025, 51(8): 1991-2008. |
| [8] | HE Hong-Li, ZHANG Yu-Han, YANG Jing, CHENG Yun-Qing, ZHAO Yang, LI Xing-Nuo, SI Hong-Liang, ZHANG Xing-Zheng, YANG Xiang-Dong. Creation and physiological analysis of an e1-as gene mutant in soybean [J]. Acta Agronomica Sinica, 2025, 51(8): 2228-2239. |
| [9] | HU Meng, SHA Dan, ZHANG Sheng-Rui, GU Yong-Zhe, ZHANG Shi-Bi, LI Jing, SUN Jun-Ming, QIU Li-Juan, LI Bin. QTL mapping and candidate gene screening for branch number in soybean [J]. Acta Agronomica Sinica, 2025, 51(7): 1747-1756. |
| [10] | YAN Zhi-Lan, ZHAO Qin, CHANG Tian-Da, WANG Yi-Ming, WANG Bi-Hui, WANG Peng, HUANG Chun-Guo, ZHANG Hui, WANG Li-Xiang, HAO Xiao-Peng, ZHAO Bo. Genome-wide identification and characterization of Alternative oxidase (AOX) genes in leguminous crops and their expression patterns in response to abiotic stresses in common bean [J]. Acta Agronomica Sinica, 2025, 51(7): 1769-1783. |
| [11] | WANG Qiong, ZOU Dan-Xia, CHEN Xing-Yun, ZHANG Wei, ZHANG Hong-Mei, LIU Xiao-Qing, JIA Qian-Ru, WEI Li-Bin, CUI Xiao-Yan, CHEN Xin, WANG Xue-Jun, CHEN Hua-Tao. Genome-wide association analysis and candidate genes prediction of flowering time and maturity date traits in soybean (Glycine max L.) [J]. Acta Agronomica Sinica, 2025, 51(6): 1558-1568. |
| [12] | YIN Cong-Cong, LI Rui-Qi, YUE Pei-Yao, LI Chen, NIU Jing-Ping, ZHAO Jin-Zhong, DU Wei-Jun, YUE Ai-Qin. Establishment and application of a visual detection method for soybean mosaic virus SC15 based on closed dumbbell mediated isothermal amplification [J]. Acta Agronomica Sinica, 2025, 51(5): 1248-1260. |
| [13] | GUO Bing, QIN Jia-Fan, LI Na, SONG Meng-Yao, WANG Li-Ming, LI Jun-Xia, MA Xiao-Qian. Genome-wide identification and expression analysis of SHMT gene family in foxtail millet (Setaria italica L.) [J]. Acta Agronomica Sinica, 2025, 51(3): 586-5897. |
| [14] | XU Rui, HE Miao-Hua, WANG Hao, LI Wei, REN Jie, XIA Zhi-Qiang. Spatial transcriptomic analysis of soybean embryonic responses to X-ray irradiation [J]. Acta Agronomica Sinica, 2025, 51(12): 3121-3132. |
| [15] | LI Wan, CHANG Zi-Rui, LU Yao, SHEN Ri-Min, ZHAO Yong-Ping, BAI Xiao-Dong. Identification of RAV family in 25 different plant species and expression analysis of RAV genes in potato [J]. Acta Agronomica Sinica, 2025, 51(11): 2944-2957. |
|
||