Cited by 233Plant Stress Responses and TolerancePlant Molecular Biology ResearchPlant-Microbe Interactions and Immunity

The DOI matches its Crossref record; 331 of the 331 references it cites were found in a registry or an index.

Engineering salinity tolerance in plants: progress and prospects

Wani, Shabir Hussain, Kumar, Vinay, Khare, Tushar, Guddimalli, Rajasheker, Parveda, Maheshwari, Solymosi, Katalin, Suprasanna, Penna, Kavi Kishor, P. B.·2020·Planta

DOI 10.1007/s00425-020-03366-6

Open this paper in CoChat — free account

Abstract

Main conclusion There is a need to integrate conceptual framework based on the current understanding of salt stress responses with different approaches for manipulating and improving salt tolerance in crop plants. Soil salinity exerts significant constraints on global crop production, posing a serious challenge for plant breeders and biotechnologists. The classical transgenic approach for enhancing salinity tolerance in plants revolves by boosting endogenous defence mechanisms, often via a single-gene approach, and usually involves the enhanced synthesis of compatible osmolytes, antioxidants, polyamines, maintenance of hormone homeostasis, modification of transporters and/or regulatory proteins, including transcription factors and alternative splicing events. Occasionally, genetic manipulation of regulatory proteins or phytohormone levels confers salinity tolerance, but all these may cause undesired reduction in plant growth and/or yields. In this review, we present and evaluate novel and cutting-edge approaches for engineering salt tolerance in crop plants. First, we cover recent findings regarding the importance of regulatory proteins and transporters, and how they can be used to enhance salt tolerance in crop plants. We also evaluate the importance of halobiomes as a reservoir of genes that can be used for engineering salt tolerance in glycophytic crops. Additionally, the role of microRNAs as critical post-transcriptional regulators in plant adaptive responses to salt stress is reviewed and their use for engineering salt-tolerant crop plants is critically assessed. The potentials of alternative splicing mechanisms and targeted gene-editing technologies in understanding plant salt stress responses and developing salt-tolerant crop plants are also discussed.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1007/s00425-020-03366-6

Cites

331 of 331 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
Komor, A. C., Kim, Y. B., Packer, M. S., Zuris, J. A., & Liu, D. R. (2016) · Nature · doi:10.1038/nature17946 · Cited by 5,437
miRBase: annotating high confidence microRNAs using deep sequencing data
Kozomara, A., & Griffiths-Jones, S. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1181 · Cited by 5,073
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage
Gaudelli, N. M., Komor, A. C., Rees, H. A., Packer, M. S., Badran, A. H., Bryson, D. I., & Liu, D. R. (2017) · Nature · doi:10.1038/nature24644 · Cited by 4,184
Soil salinity: A serious environmental issue and plant growth promoting bacteria as one of the tools for its alleviation
Shrivastava, P., & Kumar, R. (2014) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2014.12.001 · Cited by 2,949
A Robust CRISPR/Cas9 System for Convenient, High-Efficiency Multiplex Genome Editing in Monocot and Dicot Plants
Ma, X., Zhang, Q., Zhu, Q., Liu, W., Chen, Y., Qiu, R., Wang, B., Yang, Z., Li, H., Lin, Y., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2015.04.007 · Cited by 2,369
Dynamic regulation of genome-wide pre-mRNA splicing and stress tolerance by the Sm-like protein LSm5 in Arabidopsis
Cui, P., Zhang, S., Ding, F. H., Ali, S., & Xiong, L. (2014) · Genome biology · doi:10.1186/gb-2014-15-1-r1 · Cited by 2,360
Mechanism of Salinity Tolerance in Plants: Physiological, Biochemical, and Molecular Characterization
Gupta, B., & Huang, B. (2014) · International Journal of Genomics · doi:10.1155/2014/701596 · Cited by 2,105
Salt Tolerance Conferred by Overexpression of a Vacuolar Na + /H + Antiport in Arabidopsis
Apse, M. P., Aharon, G. S., Snedden, W. A., & Blumwald, E. (1999) · Science · doi:10.1126/science.285.5431.1256 · Cited by 1,964
Multiplex and homologous recombination–mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9
Li, J., Norville, J. E., Aach, J., McCormack, M., Zhang, D., Bush, J., Church, G. M., & Sheen, J. (2013) · Nature Biotechnology · doi:10.1038/nbt.2654 · Cited by 1,533
A rice quantitative trait locus for salt tolerance encodes a sodium transporter
Ren, Z., Gao, J., Li, L., Cai, X., Huang, W., Chao, D., Zhu, M., Wang, Z., Luan, S., & Lin, H. (2005) · Nature Genetics · doi:10.1038/ng1643 · Cited by 1,503
Genome sequencing reveals agronomically important loci in rice using MutMap
Abe, A., Kosugi, S., Yoshida, K., Natsume, S., Takagi, H., Kanzaki, H., Matsumura, H., Yoshida, K., Mitsuoka, C., Tamiru, M., et al. (2012) · Nature Biotechnology · doi:10.1038/nbt.2095 · Cited by 1,350
Salt resistant crop plants
Roy, S. J., Negrão, S., & Tester, M. A. (2014) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2013.12.004 · Cited by 1,192
Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit
Zhang, H., & Blumwald, E. (2001) · Nature Biotechnology · doi:10.1038/90824 · Cited by 1,123
ARGOS 8 variants generated by CRISPR ‐Cas9 improve maize grain yield under field drought stress conditions
Shi, J., Gao, H., Wang, H., Lafitte, H. R., Archibald, R. L., Yang, M., Hakimi, S. M., Mo, H., & Habben, J. E. (2017) · Plant Biotechnology Journal · doi:10.1111/pbi.12603 · Cited by 1,029
Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants
Wani, S. H., Kumar, V., Shriram, V., & Sah, S. K. (2016) · The Crop Journal · doi:10.1016/j.cj.2016.01.010 · Cited by 1,000
Sodium transport in plant cells
Blumwald, E., Aharon, G. S., & Apse, M. P. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00135-8 · Cited by 994
Functions of microRNAs in plant stress responses
Sunkar, R., Li, Y.-F., & Jagadeeswaran, G. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.01.010 · Cited by 975
Overexpression of a plasma membrane Na+/H+ antiporter gene improves salt tolerance in Arabidopsis thaliana
Shi, H., Lee, B., Wu, S.-J., & Zhu, J. (2002) · Nature Biotechnology · doi:10.1038/nbt766 · Cited by 949
The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes
Assaha, D. V. M., Ueda, A., Saneoka, H., Al-Yahyai, R. A., & Yaish, M. W. F. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00509 · Cited by 916
A Calcium Sensor Homolog Required for Plant Salt Tolerance
Liu, J., & Zhu, J. (1998) · Science · doi:10.1126/science.280.5371.1943 · Cited by 873
Complexity of the Alternative Splicing Landscape in Plants
Reddy, A. S. N., Márquez, Y., Kalyna, M., & Barta, A. (2013) · The Plant Cell · doi:10.1105/tpc.113.117523 · Cited by 867
Transcription Factors and Plants Response to Drought Stress: Current Understanding and Future Directions
Joshi, R., Wani, S. H., Singh, B., Bohra, A., Dar, Z. A., Lone, A. A., Pareek, A., & Singla-Pareek, S. L. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01029 · Cited by 857
Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene
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. A., et al. (2012) · Nature Biotechnology · doi:10.1038/nbt.2120 · Cited by 854
Diverse roles of jasmonates and ethylene in abiotic stress tolerance
Kazan, K. (2015) · Trends in Plant Science · doi:10.1016/j.tplants.2015.02.001 · Cited by 850
Plant salt tolerance: adaptations in halophytes
Flowers, T. J., & Colmer, T. D. (2015) · Annals of Botany · doi:10.1093/aob/mcu267 · Cited by 838
The Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt tolerance
Liu, J., Ishitani, M., Halfter, U., Kim, C.-S., & Zhu, J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3730 · Cited by 810
A R2R3-type MYB gene, OsMYB2, is involved in salt, cold, and dehydration tolerance in rice
Yang, A., Dai, X., & Zhang, W. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/err431 · Cited by 800
The Salt Overly Sensitive (SOS) Pathway: Established and Emerging Roles
Ji, H., Pardo, J. M., Batelli, G., Oosten, M. J. V., Bressan, R. A., & Li, X. (2013) · Molecular Plant · doi:10.1093/mp/sst017 · Cited by 760
Drought- and salt-tolerant plants result from overexpression of the AVP1 H + -pump
Gaxiola, R. A., Li, J., Undurraga, S. F., Dang, L. M., Allen, G. J., Alper, S. L., & Fink, G. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191389398 · Cited by 747
Alternative Splicing at the Intersection of Biological Timing, Development, and Stress Responses
Staiger, D., & Brown, J. W. S. (2013) · The Plant Cell · doi:10.1105/tpc.113.113803 · Cited by 690
Salinity stress alleviation using arbuscular mycorrhizal fungi. A review
Porcel, R., Aroca, R., & Ruíz-Lozano, J. M. (2011) · Agronomy for Sustainable Development · doi:10.1007/s13593-011-0029-x · Cited by 661
Hydrogen Peroxide Is Involved in Abscisic Acid-Induced Stomatal Closure in Vicia faba
Zhang, X., Zhang, L., Facai, D., Gao, J., Galbraith, D. W., & Song, C. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.4.1438 · Cited by 659
Regulation of Na+ and K+ homeostasis in plants: towards improved salt stress tolerance in crop plants
Almeida, D. M., Oliveira, M. M., & Saibo, N. J. M. (2017) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2016-0106 · Cited by 647
NONCODE 2016: an informative and valuable data source of long non-coding RNAs
Zhao, Y., Li, H., Fang, S., Kang, Y., wu, W., Hao, Y., Li, Z., Bu, D., Sun, N., Zhang, M. Q., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1252 · Cited by 643
Ion Exchangers NHX1 and NHX2 Mediate Active Potassium Uptake into Vacuoles to Regulate Cell Turgor and Stomatal Function in Arabidopsis
Barragán‐Borrero, V., Leidi, E. O., Andrés, Z., Rubio, L., Luca, A. D., Fernández, J. A., Cubero, B., & Pardo, J. M. (2012) · The Plant Cell · doi:10.1105/tpc.111.095273 · Cited by 631
A CRISPR–Cpf1 system for efficient genome editing and transcriptional repression in plants
Tang, X. D., Lowder, L. G., Zhang, T., Malzahn, A. A., Zheng, X., Voytas, D. F., Zhong, Z., Chen, Y., Ren, Q., Li, Q., et al. (2017) · Nature Plants · doi:10.1038/nplants.2017.18 · Cited by 619
Large chromosomal deletions and heritable small genetic changes induced by CRISPR/Cas9 in rice
Zhou, H., Liu, B., Weeks, D. P., Spalding, M. H., & Yang, B. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku806 · Cited by 609
Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development
Demidchik, V. V., & Maathuis, F. J. M. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02128.x · Cited by 603
Genomics, Physiology, and Molecular Breeding Approaches for Improving Salt Tolerance
Ismail, A. M., & Horie, T. (2017) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042916-040936 · Cited by 591
Shoot Na+ Exclusion and Increased Salinity Tolerance Engineered by Cell Type–Specific Alteration of Na+ Transport in Arabidopsis
Møller, I. S., Gilliham, M., Jha, D., Mayo, G. M., Roy, S. J., Coates, J. C., Haseloff, J. P., & Tester, M. A. (2009) · The Plant Cell · doi:10.1105/tpc.108.064568 · Cited by 563
Plant proton pumps
Gaxiola, R. A., Palmgren, M. B., & Schumacher, K. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.03.050 · Cited by 559
Characterizing the Saltol Quantitative Trait Locus for Salinity Tolerance in Rice
Thomson, M. J., Ocampo, M. D., Egdane, J. A., Rahman, M. A., Sajise, A. G. C., Adorada, D. L., Tumimbang-Raiz, E., Blumwald, E., Seraj, Z. I., Singh, R. K., et al. (2010) · Rice · doi:10.1007/s12284-010-9053-8 · Cited by 551
Na+ transport in plants
Apse, M. P., & Blumwald, E. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.04.014 · Cited by 516
MicroRNA: a new target for improving plant tolerance to abiotic stress
Zhang, B. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv013 · Cited by 510
Alternative splicing in plants – coming of age
Syed, N. H., Kalyna, M., Márquez, Y., Barta, A., & Brown, J. W. S. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.06.001 · Cited by 508
Expanded base editing in rice and wheat using a Cas9-adenosine deaminase fusion
Li, C., Zong, Y., Wang, Y., Jin, S., Zhang, D., Song, Q., Zhang, R., & Gao, C. (2018) · Genome biology · doi:10.1186/s13059-018-1443-z · Cited by 507
Sodium (Na+) homeostasis and salt tolerance of plants
Hasegawa, P. M. (2013) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2013.03.001 · Cited by 499
Major genes for Na+ exclusion, Nax1 and Nax2 (wheat HKT1;4 and HKT1;5), decrease Na+ accumulation in bread wheat leaves under saline and waterlogged conditions
James, R. A., Blake, C., Byrt, C. S., & Munns, R. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err003 · Cited by 489
Sodium transport in plants: a critical review
Kronzucker, H. J., & Britto, D. T. (2010) · New Phytologist · doi:10.1111/j.1469-8137.2010.03540.x · Cited by 485
Alternative splicing and nonsense-mediated decay modulate expression of important regulatory genes in Arabidopsis
Kalyna, M., Simpson, C. G., Syed, N. H., Lewandowska, D., Marquez, Y., Kusenda, B., Marshall, J., Fuller, J., Cardle, L., McNicol, J., et al. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr932 · Cited by 480
The Arabidopsis Na+/H+ Antiporters NHX1 and NHX2 Control Vacuolar pH and K+ Homeostasis to Regulate Growth, Flower Development, and Reproduction
Bassil, E., Tajima, H., Liang, Y.-C., Ohto, M., Ushijima, K., Nakano, R., Esumi, T., Coku, A., Belmonte, M. F., & Blumwald, E. (2011) · The Plant Cell · doi:10.1105/tpc.111.089581 · Cited by 469
Temperature-dependent regulation of flowering by antagonistic FLM variants
Posé, D., Verhage, L., Ott, F., Yant, L. J., Mathieu, J., Angenent, G. C., Immink, R. G. H., & Schmid, M. (2013) · Nature · doi:10.1038/nature12633 · Cited by 462
Plant Genome Engineering with Sequence-Specific Nucleases
Voytas, D. F. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042811-105552 · Cited by 462
Overexpression of microRNA OsmiR397 improves rice yield by increasing grain size and promoting panicle branching
Zhang, Y., Yu, Y., Wang, C., Li, Z.-Y., Liu, Q., Xu, J., Liao, J., Wang, X., Qu, L., Chen, F., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2646 · Cited by 458
Overexpression of SOS (Salt Overly Sensitive) Genes Increases Salt Tolerance in Transgenic Arabidopsis
Yang, Q., Chen, Z., Zhou, X., Yin, H., Li, X., Xin, X., Hong, X., Zhu, J., & Gong, Z. (2008) · Molecular Plant · doi:10.1093/mp/ssn058 · Cited by 449
Comprehensive analysis of rice DREB2-type genes that encode transcription factors involved in the expression of abiotic stress-responsive genes
Matsukura, S., Mizoi, J., Yoshida, T., Todaka, D., Ito, Y., Maruyama, K., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2010) · Molecular Genetics and Genomics · doi:10.1007/s00438-009-0506-y · Cited by 444
Vacuolar H+-pyrophosphatase
Maeshima, M. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00130-9 · Cited by 439
Precise Editing of a Target Base in the Rice Genome Using a Modified CRISPR/Cas9 System
Lu, Y., & Zhu, J. (2016) · Molecular Plant · doi:10.1016/j.molp.2016.11.013 · Cited by 423
OsSAPK2 Confers Abscisic Acid Sensitivity and Tolerance to Drought Stress in Rice
Lou, D., Wang, H., Liang, G., & Yu, D. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00993 · Cited by 420
Breeding and Domesticating Crops Adapted to Drought and Salinity: A New Paradigm for Increasing Food Production
Ana Maria, F. I. T. A., Rodríguez‐Burruezo, A., Boşcaiu, M., Prohens, J., & Vicente, Ó. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00978 · Cited by 413
Regulation of Vacuolar Na+/H+ Exchange in Arabidopsis thaliana by the Salt-Overly-Sensitive (SOS) Pathway
Qiu, Q.-S., Guo, Y., Quintero, F. J., Pardo, J. M., Schumaker, K. S., & Zhu, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307982200 · Cited by 398
Overexpression of OsMYB48-1, a Novel MYB-Related Transcription Factor, Enhances Drought and Salinity Tolerance in Rice
Xiong, H., Li, J., Liu, P., Duan, J., Zhao, Y., Guo, X., Yang, L., Zhang, H., Ali, J., & Li, Z. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092913 · Cited by 391
MicroRNAs As Potential Targets for Abiotic Stress Tolerance in Plants
Shriram, V., Kumar, V., Devarumath, R. M., Khare, T. R., & Wani, S. H. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00817 · Cited by 385
Salt stress under the scalpel – dissecting the genetics of salt tolerance
Morton, M. J. L., Awlia, M., Al‐Tamimi, N., Saadé, S., Pailles, Y., Negrão, S., & Tester, M. A. (2018) · The Plant Journal · doi:10.1111/tpj.14189 · Cited by 378
The genome of the extremophile crucifer Thellungiella parvula
Dassanayake, M., Oh, D., Haas, J. S., Hernandez, A. G., Hong, H., Ali, S., Yun, D., Bressan, R. A., Zhu, J., Bohnert, H. J., et al. (2011) · Nature Genetics · doi:10.1038/ng.889 · Cited by 375
Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants
Osakabe, Y., Watanabe, T., Sugano, S. S., Ueta, R., Ishihara, R., Shinozaki, K., & Osakabe, K. (2016) · Scientific Reports · doi:10.1038/srep26685 · Cited by 375
The Expanding Family of Eucaryotic Na+/H+Exchangers
Counillon, L., & Pouysségur, J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.1.1 · Cited by 371
CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons
Billon, P., Bryant, E. E., Joseph, S. A., Nambiar, T. S., Hayward, S. B., Rothstein, R., & Ciccia, A. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.08.008 · Cited by 363
Constitutive activation of a plasma membrane H+‐ATPase prevents abscisic acid‐mediated stomatal closure
Merlot, S., Leonhardt, N., Fenzi, F., Valon, C., Costa, J. M., Piette, L., Vavasseur, A., Genty, B., Boivin, K., Müller, A., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601750 · Cited by 358
Salt bladders: do they matter?
Shabala, S. N., Bose, J., & Hedrich, R. (2014) · Trends in Plant Science · doi:10.1016/j.tplants.2014.09.001 · Cited by 346
SALT-RESPONSIVE ERF1 Regulates Reactive Oxygen Species-Dependent Signaling during the Initial Response to Salt Stress in Rice
Schmidt, R., Mieulet, D., Hubberten, H., Obata, T., Hoefgen, R., Fernie, A. R., Fisahn, J., Segundo, B. S., Guiderdoni, E., Schippers, J. H. M., et al. (2013) · The Plant Cell · doi:10.1105/tpc.113.113068 · Cited by 346
Reactive Oxygen Species and Antioxidant Systems in Plants: Role and Regulation under Abiotic Stress
Khan, M., & Khan, N. A. (2017) · Springer eBooks · doi:10.1007/978-981-10-5254-5 · Cited by 346
Significance of the V‐type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level
Dietz, K., Tavakoli, N., Kluge, C., Mimura, T., Sharma, S., Harris, G. C., Chardonnens, A. N., & Golldack, D. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.363.1969 · Cited by 334
The Arabidopsis Intracellular Na+/H+ Antiporters NHX5 and NHX6 Are Endosome Associated and Necessary for Plant Growth and Development
Bassil, E., Ohto, M., Esumi, T., Tajima, H., Zhu, Z., Cagnac, O., Belmonte, M. F., Peleg, Z., Yamaguchi, T., & Blumwald, E. (2011) · The Plant Cell · doi:10.1105/tpc.110.079426 · Cited by 330
NONCODE: an integrated knowledge database of non-coding RNAs
Liu, C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gki041 · Cited by 321
Halophytes: Potential Resources for Salt Stress Tolerance Genes and Promoters
Mishra, A., & Tanna, B. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00829 · Cited by 320
Insights into salt tolerance from the genome of Thellungiella salsuginea
Wu, H., Zhang, Z., Wang, J., Oh, D., Dassanayake, M., Liu, B., Huang, Q., Sun, H., Xia, R., Wu, Y., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209954109 · Cited by 318
The Arabidopsis det3 mutant reveals a central role for the vacuolar H+-ATPase in plant growth and developmentPreprint
Schumacher, K., Vafeados, D. K., McCarthy, M., Sze, H., Wilkins, T., & Chory, J. (1999) · Genes & Development · doi:10.1101/gad.13.24.3259 · Cited by 315
Over‐expression of an Na + ‐ and K + ‐permeable HKT transporter in barley improves salt tolerance
Ahmad, M. A., Oomen, R. J. F. J., Isayenkov, S. V., Sentenac, H., Maathuis, F. J. M., & Véry, A. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04701.x · Cited by 311
Halotolerant Rhizobacteria Promote Growth and Enhance Salinity Tolerance in Peanut
Sharma, S., Kulkarni, J., & Jha, B. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01600 · Cited by 309
Introduction of a Na+/H+ antiporter gene from Atriplex gmelini confers salt tolerance to rice
Ohta, M., Hayashi, Y., Nakashima, A., Hamada, A., Tanaka, A., Nakamura, T., & Hayakawa, T. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)03679-7 · Cited by 306
The regulatory roles of ethylene and reactive oxygen species (ROS) in plant salt stress responses
Zhang, M., Smith, J. A. C., Harberd, N. P., & Jiang, C. (2016) · Plant Molecular Biology · doi:10.1007/s11103-016-0488-1 · Cited by 306
Precision genome engineering through adenine base editing in plants
Kang, B., Yun, J., Kim, S., Shin, Y., Ryu, J., Choi, M., Woo, J. W., & Kim, J. (2018) · Nature Plants · doi:10.1038/s41477-018-0178-x · Cited by 306
Applying CRISPR/Cas for genome engineering in plants: the best is yet to come
Puchta, H. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2016.11.011 · Cited by 305
Chloroplast function and ion regulation in plants growing on saline soils: lessons from halophytes
Bose, J., Munns, R., Shabala, S. N., Gilliham, M., Pogson, B. J., & Tyerman, S. D. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx142 · Cited by 301
The ins and outs of intracellular ion homeostasis: NHX-type cation/H + transporters
Bassil, E., & Blumwald, E. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.08.002 · Cited by 300
Expression of an Arabidopsis vacuolar H+‐pyrophosphatase gene (AVP1) in cotton improves drought‐ and salt tolerance and increases fibre yield in the field conditions
Pasapula, V., Shen, G., Kuppu, S., Paéz-Valencia, J., Mendoza, M., Hou, P., Chen, J., Qiu, X., Zhu, L., Zhang, X., et al. (2010) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2010.00535.x · Cited by 297
Mechanisms of sodium uptake by roots of higher plants
Zhang, J., Flowers, T. J., & Wang, S. (2009) · Plant and Soil · doi:10.1007/s11104-009-0076-0 · Cited by 296
Salt stress or salt shock: which genes are we studying?
Shavrukov, Y. N. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers316 · Cited by 294
TaNAC29, a NAC transcription factor from wheat, enhances salt and drought tolerance in transgenic Arabidopsis
Huang, Q., Wang, Y., Li, B., Chang, J., Chen, M., Li, K., Yang, G., & He, G. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0644-9 · Cited by 292
miRDeep-P: a computational tool for analyzing the microRNA transcriptome in plants
Yang, X., & Li, L. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr430 · Cited by 277
mirEX 2.0 - an integrated environment for expression profiling of plant microRNAs
Zieleziński, A., Dolata, J., Alaba, S., Kruszka, K., Pacak, A. M., Świda-Barteczka, A., Knop, K., Stępień, A., Bielewicz, D., Pietrykowska, H., et al. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0533-2 · Cited by 275
A plastidial sodium-dependent pyruvate transporter
Furumoto, T., Yamaguchi, T., Ohshima-Ichie, Y., Nakamura, M., Tsuchida-Iwata, Y., Shimamura, M., Ohnishi, J.-I., Hata, S., Gowik, U., Westhoff, P., et al. (2011) · Nature · doi:10.1038/nature10250 · Cited by 263
Salinity tolerance in soybean is modulated by natural variation in G m SALT 3
Guan, R., Qu, Y., Guo, Y., Yu, L., Liu, Y., Jiang, J., Chen, J., Ren, Y., Liu, G., Tian, L., et al. (2014) · The Plant Journal · doi:10.1111/tpj.12695 · Cited by 263
Ganglion-specific splicing of TRPV1 underlies infrared sensation in vampire bats
Gracheva, E. O., Cordero-Morales, J. F., González‐Carcacía, J. A., Ingolia, N. T., Manno, C. D., Aranguren, C. I., Weissman, J. S., & Julius, D. J. (2011) · Nature · doi:10.1038/nature10245 · Cited by 260
RNAcentral: a comprehensive database of non-coding RNA sequences
Petrov, A. I., Kay, S., Kalvari, I., Howe, K., Gray, K. A., Bruford, E. A., Kersey, P. J., Cochrane, G., Finn, R. D., Bateman, A. G., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1008 · Cited by 258
Arabidopsis Plasma Membrane Proteomics Identifies Components of Transport, Signal Transduction and Membrane Trafficking
Alexandersson, E., Saalbach, G., Larsson, C. U., & Kjellbom, P. O. (2004) · Plant and Cell Physiology · doi:10.1093/pcp/pch209 · Cited by 254
The evolution of halophytes, glycophytes and crops, and its implications for food security under saline conditions
Cheeseman, J. M. (2014) · New Phytologist · doi:10.1111/nph.13217 · Cited by 253
RNA interference: concept to reality in crop improvement
Saurabh, S., Vidyarthi, A. S., & Prasad, D. (2014) · Planta · doi:10.1007/s00425-013-2019-5 · Cited by 252
PNRD: a plant non-coding RNA database
Yi, X., Zhang, Z., Ling, Y., Xu, W., & Su, Z. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1162 · Cited by 251
Overexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana
Brini, F., Hanin, M., Lumbreras, V., Amara, I., Khoudi, H., Hassairi, A., Pagès, M., & Masmoudi, K. (2007) · Plant Cell Reports · doi:10.1007/s00299-007-0412-x · Cited by 248
Subcellular compartmentation of pyrophosphate and alkaline pyrophosphatase in leaves
Weiner, H., Stitt, M. D., & Heldt, H. W. (1987) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(87)90143-5 · Cited by 244
Regulation of Na+ fluxes in plants
Maathuis, F. J. M., Ahmad, I., & Patishtan-Pérez, J. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00467 · Cited by 242
Back to the future: revisiting MAS as a tool for modern plant breeding
Cobb, J. N., Biswas, P. S., & Platten, J. D. (2018) · Theoretical and Applied Genetics · doi:10.1007/s00122-018-3266-4 · Cited by 236
Methods and Applications of CRISPR-Mediated Base Editing in Eukaryotic Genomes
Hess, G. T., Tycko, J., Yao, D., & Bassik, M. C. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.09.029 · Cited by 234
HKT transporters mediate salt stress resistance in plants: from structure and function to the field
Hamamoto, S., Horie, T., Hauser, F., Deinlein, U., Schroeder, J. I., & Uozumi, N. (2014) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2014.11.025 · Cited by 227
Salt-tolerant genes from halophytes are potential key players of salt tolerance in glycophytes
Himabindu, Y., Chakradhar, T., Reddy, M. C., Kanygin, A., Redding, K., & Chandrasekhar, T. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.11.010 · Cited by 224
The Cytosolic Protein Response as a Subcomponent of the Wider Heat Shock Response in Arabidopsis
Sugio, A., Dreos, R., Aparicio, F., & Maule, A. J. (2009) · The Plant Cell · doi:10.1105/tpc.108.062596 · Cited by 218
Potential utilization of NAC transcription factors to enhance abiotic stress tolerance in plants by biotechnological approach
Tran, L. P., Nishiyama, R., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2010) · GM Crops · doi:10.4161/gmcr.1.1.10569 · Cited by 216
SKIP Is a Component of the Spliceosome Linking Alternative Splicing and the Circadian Clock in Arabidopsis
Wang, X., Wu, F., Xie, Q., Wang, H., Wang, Y., Yue, Y., Gahura, O., Ma, S., Liu, L., Cao, Y., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.100081 · Cited by 216
Thellungiella halophila, a salt‐tolerant relative of Arabidopsis thaliana, possesses effective mechanisms to discriminate between potassium and sodium
Volkov, V. S., WANG, B., DOMINY, P. J., Fricke, W., & Anna Amtmann, A. (2003) · Plant Cell & Environment · doi:10.1046/j.0016-8025.2003.01116.x · Cited by 214
Expanding the base editing scope in rice by using Cas9 variants
Hua, K., Tao, X., & Zhu, J. (2018) · Plant Biotechnology Journal · doi:10.1111/pbi.12993 · Cited by 214
Novel perspectives for the engineering of abiotic stress tolerance in plants
Cabello, J. V., Lodeyro, A. F., & Zurbriggen, M. D. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2013.09.011 · Cited by 209
Structure, function and regulation of the plant vacuolar H+-translocating ATPase
Ratajczak, R. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00129-2 · Cited by 209
The CRISPR–Cas system for plant genome editing: advances and opportunities
Kumar, V. S., & Jain, M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru429 · Cited by 207
SOS1 gene overexpression increased salt tolerance in transgenic tobacco by maintaining a higher K+/Na+ ratio
Yue, Y., Zhang, M., Zhang, J., Duan, L., & Li, Z. (2011) · Journal of Plant Physiology · doi:10.1016/j.jplph.2011.10.007 · Cited by 205
Calcium mediates root K+/Na+ homeostasis in poplar species differing in salt tolerance
Sun, J., Dai, S., Wang, R., Chen, S., Li, N., Zhou, X., Lu, C., Shen, X., Zheng, X., Hu, Z., et al. (2009) · Tree Physiology · doi:10.1093/treephys/tpp048 · Cited by 205
Enhanced salt tolerance of transgenic poplar plants expressing a manganese superoxide dismutase from Tamarix androssowii
Wang, Y. C., Qu, G. Z., Li, H. Y., Wu, Y. J., Wang, C., Liu, G. F., & Yang, C. P. (2009) · Molecular Biology Reports · doi:10.1007/s11033-009-9884-9 · Cited by 203
Increasing seed mass and oil content in transgenic Arabidopsis by the overexpression of wri1-like gene from Brassica napus
Liu, J., Hua, W., Zhan, G., Wei, F., Wang, X., Liu, G., & Wang, H. (2009) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2009.09.007 · Cited by 201
Salinity stress-tolerant and -sensitive rice (Oryza sativa L.) regulate AKT1-type potassium channel transcripts differently
Golldack, D., Quigley, F. R., Michalowski, C. B., Kamasani, U. R., & Bohnert, H. J. (2003) · Plant Molecular Biology · doi:10.1023/a:1020763218045 · Cited by 200
Rapid regulation of the plasma membrane H+-ATPase activity is essential to salinity tolerance in two halophyte species, Atriplex lentiformis and Chenopodium quinoa
Bose, J., Rodrigo-Moreno, A., Lai, D., Xie, Y., Shen, W., & Shabala, S. N. (2014) · Annals of Botany · doi:10.1093/aob/mcu219 · Cited by 199
Expression of OsDREB2A transcription factor confers enhanced dehydration and salt stress tolerance in rice (Oryza sativa L.)
Mallikarjuna, G. B., Mallikarjuna, K., Reddy, M. K., & Kaul, T. (2011) · Biotechnology Letters · doi:10.1007/s10529-011-0620-x · Cited by 198
Salt Stress Triggers Phosphorylation of the Arabidopsis Vacuolar K+ Channel TPK1 by Calcium-Dependent Protein Kinases (CDPKs)
Latz, A., Mehlmer, N., Zapf, S., Mueller, T. D., Wurzinger, B., Pfister, B., Csaszar, E., Hedrich, R., Teige, M., & Becker, D. (2012) · Molecular Plant · doi:10.1093/mp/sss158 · Cited by 197
Over-expression of sly-miR156a in tomato results in multiple vegetative and reproductive trait alterations and partial phenocopy of the sft mutant
Zhang, X., Zou, Z., Zhang, J., Zhang, Y., Han, Q., Hu, T., Xu, X., Liu, H., Li, J., & Ye, Z. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.12.036 · Cited by 197
Expression of a Constitutively Activated Plasma Membrane H + -ATPase Alters Plant Development and Increases Salt Tolerance
Gévaudant, F., Duby, G., von Stedingk, E., Zhao, R., Morsomme, P., & Boutry, M. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.103762 · Cited by 196
A Two-Staged Model of Na+ Exclusion in Rice Explained by 3D Modeling of HKT Transporters and Alternative Splicing
Cotsaftis, O., Plett, D., Shirley, N. J., Tester, M. A., & Hrmová, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039865 · Cited by 194
Molecular cloning and sequence of cDNA encoding the pyrophosphate-energized vacuolar membrane proton pump of Arabidopsis thaliana.
Sarafian, V., Kim, Y., Poole, R. J., & Rea, P. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.5.1775 · Cited by 190
A DEAD Box RNA Helicase Is Critical for Pre-mRNA Splicing, Cold-Responsive Gene Regulation, and Cold Tolerance in Arabidopsis
Guan, Q., Wu, J., Zhang, Y., Jiang, C., Liu, R., Chai, C., & Zhu, J. (2013) · The Plant Cell · doi:10.1105/tpc.112.108340 · Cited by 189
Regulation by salt of vacuolar H + -ATPase and H + -pyrophosphatase activities and Na + /H + exchange
Silva, P., & Gerós, H. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.8.9236 · Cited by 184
Novel NAC Transcription Factor TaNAC67 Confers Enhanced Multi-Abiotic Stress Tolerances in Arabidopsis
Mao, X., Chen, S., Li, A., Zhai, C., & Jing, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084359 · Cited by 184
Precise insertion and guided editing of higher plant genomes using Cpf1 CRISPR nucleases
Begemann, M. B., Gray, B. N., January, E., Gordon, G. C., He, Y., Liu, H., Wu, X., Brutnell, T. P., Mockler, T. C., & Oufattole, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-11760-6 · Cited by 183
How do vacuolar NHX exchangers function in plant salt tolerance?
Jiang, X., Leidi, E. O., & Pardo, J. M. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.7.11767 · Cited by 182
The SbSOS1 gene from the extreme halophyte Salicornia brachiata enhances Na+loading in xylem and confers salt tolerance in transgenic tobacco
Yadav, N. S., Shukla, P. S., Jha, A., Agarwal, P. K., & Jha, B. (2012) · BMC Plant Biology · doi:10.1186/1471-2229-12-188 · Cited by 182
Integrating Omics and Alternative Splicing Reveals Insights into Grape Response to High Temperature
Jiang, J., Liu, X., Liu, C., Liu, G., Li, S., & Wang, L. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01305 · Cited by 182
Thellungiella halophila, a salt‐tolerant relative of Arabidopsis thaliana, has specific root ion‐channel features supporting K+/Na+ homeostasis under salinity stress
Volkov, V. S., & Amtmann, A. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02876.x · Cited by 181
Overexpression of an H+-PPase Gene from Thellungiella halophila in Cotton Enhances Salt Tolerance and Improves Growth and Photosynthetic Performance
Lv, S., Zhang, K., Gao, Q., Lian, L., Song, Y., & Zhang, J. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn090 · Cited by 178
Low-Affinity Na+ Uptake in the HalophyteSuaeda maritima
Wang, S., Zhang, J., & Flowers, T. J. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.104315 · Cited by 177
Overexpression of soybean miR172c confers tolerance to water deficit and salt stress, but increases ABA sensitivity in transgenic Arabidopsis thaliana
Li, W., Wang, T., Zhang, Y., & Li, Y. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv450 · Cited by 174
Rice K+ uptake channel OsAKT1 is sensitive to salt stress
Fuchs, I., Stölzle, S., Ivashikina, N., & Hedrich, R. (2004) · Planta · doi:10.1007/s00425-004-1437-9 · Cited by 172
A rice stress-responsive NAC gene enhances tolerance of transgenic wheat to drought and salt stresses
Saad, A. S. I., Li, X., Li, H., Huang, T., Gao, C.-S., Guo, M., Cheng, W., Zhao, G., & Liao, Y. (2013) · Plant Science · doi:10.1016/j.plantsci.2012.12.016 · Cited by 170
SKIP Confers Osmotic Tolerance during Salt Stress by Controlling Alternative Gene Splicing in Arabidopsis
Feng, J., Li, J., Gao, Z., Lu, Y., Yu, J., Zheng, Q., Yan, S., Zhang, W., He, H., Ma, L., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2015.01.011 · Cited by 169
Overexpression of the tomato K+/H+ antiporter LeNHX2 confers salt tolerance by improving potassium compartmentalization
Rodríguez‐Rosales, M. P., Jiang, X., Gálvez, F. J., Aranda, M. N., Cubero, B., & Venema, K. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02461.x · Cited by 168
Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation
Kriechbaumer, V., Wang, P., Hawes, C. R., & Abell, B. M. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04866.x · Cited by 164
Constitutive Expression of Rice MicroRNA528 Alters Plant Development and Enhances Tolerance to Salinity Stress and Nitrogen Starvation in Creeping Bentgrass
Yuan, S., Li, Z., Li, D., Yuan, N. Y., Hu, Q., & Luo, H. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00899 · Cited by 163
Transcriptome Analyses of a Salt-Tolerant Cytokinin-Deficient Mutant Reveal Differential Regulation of Salt Stress Response by Cytokinin Deficiency
Nishiyama, R., Le, D. T., Watanabe, Y., Matsui, A., Tanaka, M., Seki, M., Yamaguchi‐Shinozaki, K., Shinozaki, K., & Tran, L. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032124 · Cited by 162
Improved Salinity Tolerance of Rice Through Cell Type-Specific Expression of AtHKT1;1
Plett, D., Safwat, G., Gilliham, M., Møller, I. S., Roy, S. J., Shirley, N. J., Jacobs, A. K., Johnson, A. A. T., & Tester, M. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012571 · Cited by 162
Salinity tolerance in plants. Quantitative approach to ion transport starting from halophytes and stepping to genetic and protein engineering for manipulating ion fluxes
Volkov, V. S. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00873 · Cited by 161
Relationship between multiple paternity and reproductive parameters for Podocnemis sextuberculata (Testudines: Podocnemididae) in the Trombetas River, Brazil
Pereira, F. F., Bernardes, V. C. D., Eisemberg, C. C., Fantin, C., & Vogt, R. C. (2016) · Genetics and Molecular Research · doi:10.4238/gmr.15017335 · Cited by 161
Co-expression of the Suaeda salsa SsNHX1 and Arabidopsis AVP1 confer greater salt tolerance to transgenic rice than the single SsNHX1
Zhao, F., Zhang, X., Li, P., Zhao, Y., & Zhang, H. (2006) · Molecular Breeding · doi:10.1007/s11032-006-9005-6 · Cited by 155
Transgenic salt‐tolerant sugar beet ( Beta vulgaris L.) constitutively expressing an Arabidopsis thaliana vacuolar Na + /H + antiporter gene, AtNHX3 , accumulates more soluble sugar but less salt in storage roots
Liu, H., Wang, Q., YU, M., Zhang, Y., Wu, Y., & Zhang, H. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01838.x · Cited by 155
Evidence for a role in growth and salt resistance of a plasma membrane H+‐ATPase in the root endodermis
Vitart, V., Baxter, I. R., Doerner, P. W., & Harper, J. F. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01081.x · Cited by 155
Emerging concepts of potassium homeostasis in plants
Srivastava, A. K., Shankar, A., Chandran, A. K. N., Sharma, M., Jung, K., Suprasanna, P., & Pandey, G. K. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz458 · Cited by 150
Expression of the A rabidopsis vacuolar H +‐pyrophosphatase gene ( AVP 1) improves the shoot biomass of transgenic barley and increases grain yield in a saline field
Schilling, R. K., Marschner, P., Shavrukov, Y. N., Berger, B., Tester, M. A., Roy, S. J., & Plett, D. (2013) · Plant Biotechnology Journal · doi:10.1111/pbi.12145 · Cited by 149
Salt-Induced Expression of the Vacuolar H+-ATPase in the Common Ice Plant Is Developmentally Controlled and Tissue Specific
Golldack, D., & Dietz, K. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.4.1643 · Cited by 149
Over-expression of a NAC 67 transcription factor from finger millet (Eleusine coracana L.) confers tolerance against salinity and drought stress in rice
Rahman, H., Ramanathan, V., Nallathambi, J., Duraialagaraja, S., & Raveendran, M. (2016) · BMC Biotechnology · doi:10.1186/s12896-016-0261-1 · Cited by 148
Transformation of tomato with the BADH gene from Atriplex improves salt tolerance
Z.-Q., Z., F.-Q., C., Y.-X., L., & G.-X., J. (2002) · Plant Cell Reports · doi:10.1007/s00299-002-0489-1 · Cited by 146
Enhanced salt stress tolerance of rice plants expressing a vacuolar H+‐ATPase subunit c1 (SaVHAc1) gene from the halophyte grass Spartina alterniflora Löisel
Baisakh, N., Ramanarao, M. V., Rajasekaran, K., Subudhi, P. K., Janda, J., Galbraith, D. W., Vanier, C. H., & Pereira, A. (2012) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2012.00678.x · Cited by 142
Rice sodium-insensitive potassium transporter, OsHAK5, confers increased salt tolerance in tobacco BY2 cells
Horie, T., Sugawara, M., Okada, T., Taira, K., Kaothien-Nakayama, P., Katsuhara, M., Shinmyō, A., & Nakayama, H. (2010) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2010.10.014 · Cited by 139
Characterization and expression of a vacuolar Na+/H+ antiporter gene from the monocot halophyte Aeluropus littoralis
Zhang, G.-H., Su, Q., An, L., & Wu, S. J. (2007) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2007.10.022 · Cited by 135
Differential Expression of Vacuolar H+-ATPase Subunit c Genes in Tissues Active in Membrane Trafficking and Their Roles in Plant Growth as Revealed by RNAi
Padmanaban, S., Lin, X., Perera, I. Y., Kawamura, Y., & Sze, H. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.034025 · Cited by 133
Salinity Response in Chloroplasts: Insights from Gene Characterization
Suo, J., Zhao, Q., David, L., Chen, S., & Dai, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18051011 · Cited by 133
Increased vacuolar Na+/H+ exchange activity in Salicornia bigelovii Torr. in response to NaCl
Parks, G. E. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.371.1055 · Cited by 132
SOS1, HKT1;5, and NHX1 Synergistically Modulate Na+ Homeostasis in the Halophytic Grass Puccinellia tenuiflora
Zhang, W.-D., Wang, P., Bao, Z., Ma, Q., Duan, L.-J., Bao, A., Zhang, J., & Wang, S. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00576 · Cited by 132
Na+ and Cl− ions show additive effects under NaCl stress on induction of oxidative stress and the responsive antioxidative defense in rice
Khare, T. R., Kumar, V., & Kishor, P. B. K. (2014) · PROTOPLASMA · doi:10.1007/s00709-014-0749-2 · Cited by 130
Functional validation of a novel isoform of Na+/H+ antiporter from Pennisetum glaucum for enhancing salinity tolerance in rice
Verma, D., Singla-Pareek, S. L., Rajagopal, D., Reddy, M. K., & Sopory, S. K. (2007) · Journal of Biosciences · doi:10.1007/s12038-007-0061-9 · Cited by 129
Crystal structure of a potassium ion transporter, TrkH
Cao, Y., Jin, X., Huang, H., Derebe, M. G., Levin, E. J., Kabaleeswaran, V., Pan, Y., Punta, M., Love, J. D., Weng, J., et al. (2011) · Nature · doi:10.1038/nature09731 · Cited by 128
Cosuppression of a Plasma Membrane H+-ATPase Isoform Impairs Sucrose Translocation, Stomatal Opening, Plant Growth, and Male Fertility
Zhao, R., Dielen, V., Kinet, J., & Boutry, M. (2000) · The Plant Cell · doi:10.1105/tpc.12.4.535 · Cited by 127
Comparison between Arabidopsis and Rice for Main Pathways of K+ and Na+ Uptake by Roots
Nieves‐Cordones, M., Martı́nez, V., Benito, B., & Rubio, F. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00992 · Cited by 127
Co‐expression of tonoplast Cation/H+ antiporter and H+‐pyrophosphatase from xerophyte Zygophyllum xanthoxylum improves alfalfa plant growth under salinity, drought and field conditions
Bao, A., Du, B., Touil, L., Kang, P., Wang, Q., & Wang, S. (2015) · Plant Biotechnology Journal · doi:10.1111/pbi.12451 · Cited by 126
Enhancing salt tolerance in quinoa by halotolerant bacterial inoculation
Yang, A., Akhtar, S. S., Iqbal, S., Amjad, M., Naveed, M., Zahir, Z. A., & Jacobsen, S. (2016) · Functional Plant Biology · doi:10.1071/fp15265 · Cited by 122
Allelic variants of OsHKT1;1 underlie the divergence between indica and japonica subspecies of rice (Oryza sativa) for root sodium content
Campbell, M. T., Bandillo, N. B., Al-Burki, F. R., Sharma, S., Liu, K., Du, Q., Schmitz, A. J., Zhang, C., Véry, A., Lorenz, A. J., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006823 · Cited by 122
Sargassum muticum and Jania rubens regulate amino acid metabolism to improve growth and alleviate salinity in chickpea
Latef, A. A. H. A., Srivastava, A. K., Saber, H., Alwaleed, E. A., & Tran, L. P. (2017) · Scientific Reports · doi:10.1038/s41598-017-07692-w · Cited by 122
CarNAC4, a NAC-type chickpea transcription factor conferring enhanced drought and salt stress tolerances in Arabidopsis
Yu, X., Liu, Y., Wang, S., Yuan, T., Wang, Z., Shu, Y., Peng, H., Mijiti, A., Wang, Z., Zhang, H., et al. (2015) · Plant Cell Reports · doi:10.1007/s00299-015-1907-5 · Cited by 121
Plant small RNAs: the essential epigenetic regulators of gene expression for salt-stress responses and tolerance
Kumar, V., Khare, T. R., Shriram, V., & Wani, S. H. (2017) · Plant Cell Reports · doi:10.1007/s00299-017-2210-4 · Cited by 121
An alternatively spliced heat shock transcription factor, Os HSFA 2dI, functions in the heat stress‐induced unfolded protein response in rice
Cheng, Q., Zhou, Y., Liu, Z., Zhang, L., Song, G., Guo, Z., Wang, W., Qu, X., Zhu, Y., & Yang, D. (2014) · Plant Biology · doi:10.1111/plb.12267 · Cited by 120
Function genomics of abiotic stress tolerance in plants: a CRISPR approach
Jain, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00375 · Cited by 118
Ethanol Enhances High-Salinity Stress Tolerance by Detoxifying Reactive Oxygen Species in Arabidopsis thaliana and Rice
Nguyen, H. M., Sako, K., Matsui, A., Suzuki, Y., Mostofa, M. G., Ha, C. V., Tanaka, M., Tran, L. P., Habu, Y., & Seki, M. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01001 · Cited by 118
Enhanced Expression of AtNHX1, in Transgenic Groundnut (Arachis hypogaea L.) Improves Salt and Drought Tolerence
Asif, M. A., Zafar, Y., Iqbal, J., Iqbal, M. M., Rashid, U., Ali, G. M., Arif, A., & Nazir, F. (2011) · Molecular Biotechnology · doi:10.1007/s12033-011-9399-1 · Cited by 117
Over-expression of the Peroxisomal Ascorbate Peroxidase (SbpAPX) Gene Cloned from Halophyte Salicornia brachiata Confers Salt and Drought Stress Tolerance in Transgenic Tobacco
Singh, N., Mishra, A., & Jha, B. (2013) · Marine Biotechnology · doi:10.1007/s10126-013-9548-6 · Cited by 117
miRA: adaptable novel miRNA identification in plants using small RNA sequencing data
Evers, M., Huttner, M., Dueck, A., Meister, G., & Engelmann, J. C. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0798-3 · Cited by 117
Expression of the AKT1-type K+ channel gene from Puccinellia tenuiflora, PutAKT1, enhances salt tolerance in Arabidopsis
Ardie, S. W., Liu, S., & Takano, T. (2010) · Plant Cell Reports · doi:10.1007/s00299-010-0872-2 · Cited by 112
Marker Aided Incorporation of Saltol, a Major QTL Associated with Seedling Stage Salt Tolerance, into Oryza sativa ‘Pusa Basmati 1121’
Babu, N. N., Krishnan, S. G., Vinod, K. K., Krishnamurthy, S. L., Singh, V. K., Singh, M. P., Singh, R., Ellur, R. K., Rai, V., Bollinedi, H., et al. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00041 · Cited by 112
Expanding the Scope of CRISPR/Cpf1-Mediated Genome Editing in Rice
Li, S., Zhang, X., Wang, W., Guo, X., Wu, Z., Du, W., Zhao, Y., & Xia, L. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.03.009 · Cited by 112
miRPlant: an integrated tool for identification of plant miRNA from RNA sequencing data
An, J., Lai, J., Sajjanhar, A., Lehman, M., & Nelson, C. C. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-275 · Cited by 111
Competitive inhibition of transcription factors by small interfering peptides
Seo, P. J., Hong, S., Kim, S., & Park, C. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.06.001 · Cited by 110
The Thellungiella salsuginea Tonoplast Aquaporin TsTIP1;2 Functions in Protection Against Multiple Abiotic Stresses
Wang, L.-L., Chen, A., Zhong, N., Liu, N., Wu, X.-M., Wang, F., Yang, C. L., Romero, M. F., & Xia, G. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pct166 · Cited by 108
Developing Transgenic Jatropha Using the SbNHX1 Gene from an Extreme Halophyte for Cultivation in Saline Wasteland
Jha, B., Mishra, A., Jha, A., & Joshi, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071136 · Cited by 108
Molecular Cloning and Characterization of a Vacuolar H+-pyrophos-phatase Gene, SsVP, from the Halophyte Suaeda salsa and its Overexpression Increases Salt and Drought Tolerance of Arabidopsis
Guo, S., Yin, H., Zhang, X., Zhao, F., Li, P., Chen, S., Zhao, Y., & Zhang, H. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-2417-6 · Cited by 107
Multiplex gene editing in rice with simplified CRISPR‐Cpf1 and CRISPR‐Cas9 systems
Wang, M., Mao, Y., Lu, Y., Wang, Z., Tao, X., & Zhu, J. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12667 · Cited by 106
NaCl Regulation of Tonoplast ATPase 70-Kilodalton Subunit mRNA in Tobacco Cells
Narasimhan, M. L., Binzel, M. L., Perez-Prat, E., Chen, Z., Nelson, D. E., Singh, N. K., Bressan, R. A., & Hasegawa, P. M. (1991) · PLANT PHYSIOLOGY · doi:10.1104/pp.97.2.562 · Cited by 105
Soybean miR172a Improves Salt Tolerance and Can Function as a Long-Distance Signal
Pan, W., Tao, J., Cheng, T., Bian, X., Wei, W., Zhang, W., Ma, B., Chen, S., & Zhang, J. (2016) · Molecular Plant · doi:10.1016/j.molp.2016.05.010 · Cited by 105
Introgression of the SbASR-1 Gene Cloned from a Halophyte Salicornia brachiata Enhances Salinity and Drought Endurance in Transgenic Groundnut (Arachis hypogaea) and Acts as a Transcription Factor
Tiwari, V., Chaturvedi, A. K., Mishra, A., & Jha, B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131567 · Cited by 103
Ectopic over-expression of peroxisomal ascorbate peroxidase (SbpAPX) gene confers salt stress tolerance in transgenic peanut (Arachis hypogaea)
Singh, N., Mishra, A., & Jha, B. (2014) · Gene · doi:10.1016/j.gene.2014.06.037 · Cited by 102
Pennisetum glaucum Na+/H+ antiporter confers high level of salinity tolerance in transgenic Brassica juncea
Rajagopal, D., Agarwal, P. K., Tyagi, W., Singla-Pareek, S. L., Reddy, M. K., & Sopory, S. K. (2006) · Molecular Breeding · doi:10.1007/s11032-006-9052-z · Cited by 101
Co-overexpressing a Plasma Membrane and a Vacuolar Membrane Sodium/Proton Antiporter Significantly Improves Salt Tolerance in Transgenic Arabidopsis Plants
Pehlivan, N., Sun, L., Jarrett, P. C., Yang, X., Mishra, N., Chen, L., Kadıoğlu, A., Shen, G., & Zhang, H. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw055 · Cited by 101
Primary responses to salt stress in a halophyte, smooth cordgrass (Spartina alterniflora Loisel.)
Baisakh, N., Subudhi, P. K., & Varadwaj, P. K. (2008) · Functional & Integrative Genomics · doi:10.1007/s10142-008-0075-x · Cited by 98
Salt tolerance and activity of antioxidative enzymes of transgenic finger millet overexpressing a vacuolar H+-pyrophosphatase gene (SbVPPase) from Sorghum bicolor
Ediga, A., Reddy, P. S., Sunita, M. S. L., Kishor, P. B. K., & Meriga, B. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.02.001 · Cited by 96
Co-expression of Pennisetum glaucum vacuolar Na+/H+ antiporter and Arabidopsis H+-pyrophosphatase enhances salt tolerance in transgenic tomato
Bhaskaran, S., & Savithramma, D. L. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err237 · Cited by 96
Co-expression of the Arabidopsis SOS genes enhances salt tolerance in transgenic tall fescue (Festuca arundinacea Schreb.)
Ma, D., Xu, W., Hui-wen, L., Jin, F.-X., Guo, L.-N., Wang, J., Dai, H.-J., & Xu, X. (2013) · PROTOPLASMA · doi:10.1007/s00709-013-0540-9 · Cited by 95
Overexpression of a Malus vacuolar Na+/H+ antiporter gene (MdNHX1) in apple rootstock M.26 and its influence on salt tolerance
Li, Y., Zhang, Y., Feng, F., Liang, D., Cheng, L., Ma, F., & Shi, S. (2010) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-010-9738-0 · Cited by 91

Research works printed but not linked: 2

FAO (2015) FAO Land and Plant Nutrition Management Service. Food and Agriculture Organization of the United Nations, Rome
Kere GM, Chen C, Guo Q, Chen J (2017) Genetics of salt tolerance in cucumber (Cucumis sativus L.) revealed by quantitative traits loci analysis. Sci Lett 5(1):22–30

Sorted by citations

Plants’ Response Mechanisms to Salinity Stress
Balasubramaniam, T., Shen, G., Esmaeili, N., & Zhang, H. (2023) · Plants · doi:10.3390/plants12122253 · Cited by 740
Plant sugars: Homeostasis and transport under abiotic stress in plants
Saddhe, A. A., Manuka, R., & Suprasanna, P. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13283 · Cited by 436
Roles of Arbuscular Mycorrhizal Fungi on Plant Growth and Performance: Importance in Biotic and Abiotic Stressed Regulation
Diagne, N., Ngom, M., Djighaly, P. I., Fall, D., Hocher, V., & Svistoonoff, S. (2020) · Diversity · doi:10.3390/d12100370 · Cited by 422
Mitigating Soil Salinity Stress with Gypsum and Bio-Organic Amendments: A Review
Bello, S. K., Alayafi, A. H., AL-Solaimani, S. G., & Abo‐Elyousr, K. A. M. (2021) · Agronomy · doi:10.3390/agronomy11091735 · Cited by 256
Role of bZIP Transcription Factors in Plant Salt Stress
Liu, H., Tang, X., Zhang, N., Li, S., & Si, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24097893 · Cited by 176

See all 233

Authors: Wani, S. H., Kumar, V., Khare, T., Guddimalli, R., Parveda, M., Solymosi, K., Suprasanna, P., & Kavi Kishor, P. B.
Affiliations: Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir (IN)
Savitribai Phule Pune University (IN)
Osmania University (IN)
Eötvös Loránd University (HU)
Bhabha Atomic Research Centre (IN)
Corresponding author: Wani, Shabir Hussain
ORCID: Wani, Shabir Hussain
Kumar, Vinay
Khare, Tushar
Solymosi, Katalin
Suprasanna, Penna
Venue: Planta
Publisher: Springer Science and Business Media LLC
Published: 2020-03-09
Volume: 251
Issue: 4
Pages: 76-76
ISSN: 0032-0935 (ISSN-L)
1432-2048
DOI: 10.1007/s00425-020-03366-6
OpenAlex: W3010616591
Cited by: 233
References: 331
Citations by year: 2026: 19 · 2025: 38 · 2024: 44 · 2023: 37 · 2022: 36 · 2021: 43 · 2020: 16
FWCI: 2.81
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: Planta (publishedVersion)
PubMed (publishedVersion)
Repository of the Academy's Library (Library of the Hungarian Academy of Sciences) (acceptedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
Keywords: salt tolerance, salt stress, cultivated plants, transgenic plants, osmolytes, antioxidants, polyamines, phytohormone homeostasis, ion transporters, transcription factors, microRNA, alternative splicing, genome editing
MeSH terms: Gene Editing, Chloroplasts, Plant Growth Regulators, Alternative Splicing, Crops, Agricultural, Genome, Plant, Potassium-Hydrogen Antiporters, Arabidopsis Proteins, Plants, Genetically Modified, RNA Interference, Quantitative Trait Loci, Salinity, Salt Tolerance, Salt-Tolerant Plants, Plant Development

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Engineering salinity tolerance in plants: progress and prospects

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks