Cited by 1,215Plant Stress Responses and TolerancePlant Molecular Biology ResearchPlant-Microbe Interactions and Immunity

The DOI matches its Crossref record; 123 of the 123 references it cites were found in a registry or an index.

Research on plant abiotic stress responses in the post‐genome era: past, present and future

Open access

Hirayama, Takashi, Shinozaki, Kazuo·2010·The Plant Journal

DOI 10.1111/j.1365-313x.2010.04124.x

Open this paper in CoChat — free account Open PDF

Abstract

Summary: Understanding abiotic stress responses in plants is an important and challenging topic in plant research. Physiological and molecular biological analyses have allowed us to draw a picture of abiotic stress responses in various plants, and determination of the Arabidopsis genome sequence has had a great impact on this research field. The availability of the complete genome sequence has facilitated access to essential information for all genes, e.g. gene products and their function, transcript levels, putative cis‐ regulatory elements, and alternative splicing patterns. These data have been obtained from comprehensive transcriptome analyses and studies using full‐length cDNA collections and T‐DNA‐ or transposon‐tagged mutant lines, which were also enhanced by genome sequence information. Moreover, studies on novel regulatory mechanisms involving use of small RNA molecules, chromatin modulation and genomic DNA modification have enabled us to recognize that plants have evolved complicated and sophisticated systems in response to complex abiotic stresses. Integrated data obtained with various ‘omics’ approaches have provided a more comprehensive picture of abiotic stress responses. In addition, research on stress responses in various plant species other than Arabidopsis has increased our knowledge regarding the mechanisms of plant stress tolerance in nature. Based on this progress, improvements in crop stress tolerance have been attempted by means of gene transfer and marker‐assisted breeding. In this review, we summarize recent progress in abiotic stress studies, especially in the post‐genomic era, and offer new perspectives on research directions for the next decade.

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 · 10.1111/j.1365-313x.2010.04124.x

Cites

123 of 123 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.

Europe-wide reduction in primary productivity caused by the heat and drought in 2003
Ciais, P., Reichstein, M., Viovy, N., Granier, A., Ogée, J., Allard, V., Aubinet, M., Buchmann, N., Bernhofer, C., Carrara, A., et al. (2005) · Nature · doi:10.1038/nature03972 · Cited by 4,153
Abiotic stress, the field environment and stress combination
Mittler, R. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.11.002 · Cited by 3,083
Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins
Park, S., Fung, P., Nishimura, N., Jensen, D. R., Fujii, H., Zhao, Y., Lumba, S., Santiago, J., Rodrigues, A., Chow, T.-F. F., et al. (2009) · Science · doi:10.1126/science.1173041 · Cited by 2,986
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105444 · Cited by 2,935
Self-citation
Salinity tolerance in halophytes*
Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789
The complex language of chromatin regulation during transcription
Berger, S. L. (2007) · Nature · doi:10.1038/nature05915 · Cited by 2,768
MicroRNAs AND THEIR REGULATORY ROLES IN PLANTS
Jones-Rhoades, M. W., Bartel, D. P., & Bartel, B. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105218 · Cited by 2,720
Gene networks involved in drought stress response and tolerance
Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl164 · Cited by 2,641
Self-citation
Drought and Salt Tolerance in Plants
Bartels, D., & Sunkar, R. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680590910410 · Cited by 2,611
Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors
Ma, Y., Szostkiewicz, I., Korte, A., Moes, D., Yang, Y., Christmann, A., & Grill, E. (2009) · Science · doi:10.1126/science.1172408 · Cited by 2,467

Show all 123 references

Sorted by citations

Items 301–400 of 1,000

Impact of abiotic stress on the regulation of cell wall biosynthesis in Populus trichocarpa
Hori, C., Yu, X., Mortimer, J. C., Sano, R., Matsumoto, T., Kikuchi, J., Demura, T., & Ohtani, M. (2020) · Plant Biotechnology · doi:10.5511/plantbiotechnology.20.0326a · Cited by 58
Wild soybean roots depend on specific transcription factors and oxidation reduction related genesin response to alkaline stress
Duanmu, H., Wang, Y., Bai, X., Cheng, S., Deyholos, M. K., Wong, G. K., Li, D., Zhu, D., Li, R., Yu, Y., et al. (2015) · Functional & Integrative Genomics · doi:10.1007/s10142-015-0439-y · Cited by 58
Global gene expression analysis using RNA-seq uncovered a new role for SR1/CAMTA3 transcription factor in salt stress
Prasad, K. V. S. K., Abdel‐Hameed, A. A. E., Xing, D., & Reddy, A. S. N. (2016) · Scientific Reports · doi:10.1038/srep27021 · Cited by 58
Systems Responses to Progressive Water Stress in Durum Wheat
Habash, D. Z., Baudo, M., Hindle, M., Powers, S. J., Platel, M. D., Mitchell, R. A. C., Saqi, M. A. S., Rawlings, C., Latiri, K., Araus, J. L., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108431 · Cited by 57
Arabidopsis Non-Coding RNA Regulation in Abiotic Stress Responses
Matsui, A., Nguyen, A., Nakaminami, K., & Seki, M. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms141122642 · Cited by 60
ERD15—An attenuator of plant ABA responses and stomatal aperture
Aalto, M. K., Helenius, E., Kariola, T., Pennanen, V., Heino, P. I., Hõrak, H., Puzõrjova, I., Kollist, H., & Palva, E. T. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.08.009 · Cited by 59
Narrowing down the targets for yield improvement in rice under normal and abiotic stress conditions via expression profiling of yield-related genes
Tripathi, A. K., Pareek, A., Sopory, S. K., & Singla-Pareek, S. L. (2012) · Rice · doi:10.1186/1939-8433-5-37 · Cited by 57
Overexpression of the RNA binding protein MhYTP1 in transgenic apple enhances drought tolerance and WUE by improving ABA level under drought condition
Guo, T., Wang, N., Xue, Y., Guan, Q., van Nocker, S., Liu, C., & Ma, F. (2018) · Plant Science · doi:10.1016/j.plantsci.2018.11.018 · Cited by 57
Expression profiles of precursor and mature microRNAs under dehydration and high salinity shock in Populus euphratica
Qin, Y., Duan, Z., Xia, X., & Yin, W. (2011) · Plant Cell Reports · doi:10.1007/s00299-011-1096-9 · Cited by 56
The ‘dark matter’ in the plant genomes: non-coding and unannotated DNA sequences associated with open chromatin
Jiang, J. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.01.005 · Cited by 57
A Soybean bZIP Transcription Factor GmbZIP19 Confers Multiple Biotic and Abiotic Stress Responses in Plant
He, Q., Cai, H., Bai, M., Zhang, M., Chen, F., Huang, Y., Priyadarshani, S. V. G. N., Chai, M., Liu, L., Liu, Y., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134701 · Cited by 55
G-protein Signaling Components GCR1 and GPA1 Mediate Responses to Multiple Abiotic Stresses in Arabidopsis
Chakraborty, N., Singh, N., Kaur, K., & Raghuram, N. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01000 · Cited by 55
Abscisic acid transcriptomic signaling varies with grapevine organ
Rattanakon, S., Ghan, R., Gambetta, G. A., Deluc, L. G., Schlauch, K. A., & Cramer, G. R. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0763-y · Cited by 55
Understanding Agriculture within the Frameworks of Cumulative Cultural Evolution, Gene-Culture Co-Evolution, and Cultural Niche Construction
Altman, A., & Mesoudi, A. (2019) · Human Ecology · doi:10.1007/s10745-019-00090-y · Cited by 55
Effect of Cold Stress on Photosynthesis of Plants and Possible Protection Mechanisms
Adam, S., & Murthy, S. D. S. (2013) · Springer eBooks · doi:10.1007/978-81-322-1620-9_12 · Cited by 55
Increased salt and drought tolerance by d-ononitol production in transgenic Arabidopsis thaliana
Ahn, C., Park, U., & Park, P. B. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.10.134 · Cited by 55
Cold Stress and Photosynthesis
Banerjee, A., & Roychoudhury, A. (2019) · Wiley eBooks · doi:10.1002/9781119501800.ch2 · Cited by 55
Genome-wide identification and functional analysis of U-box E3 ubiquitin ligases gene family related to drought stress response in Chinese white pear (Pyrus bretschneideri)
Wang, C., Song, B., Dai, Y., Zhang, S., & Huang, X. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-03024-3 · Cited by 54
Plant protease as regulator and signaling molecule for enhancing environmental stress-tolerance
Sharma, P., & Gayen, D. (2021) · Plant Cell Reports · doi:10.1007/s00299-021-02739-9 · Cited by 59
Biochar actions for the mitigation of plant abiotic stress
Imran, S., Sarker, P., Hoque, M. N., Paul, N. C., Mahamud, M. A., Chakrobortty, J., Tahjib‐Ul‐Arif, M., Latef, A. A. H. A., Hasanuzzaman, M., & Rhaman, M. S. (2022) · Australian Journal of Agricultural Research · doi:10.1071/cp21486 · Cited by 54
Epigenomics in stress tolerance of plants under the climate change
Kumar, M., Rani, K., & Goswami, P. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08539-6 · Cited by 54
Drought tolerance acquisition in Eucalyptus globulus (Labill.): A research on plant morphology, physiology and proteomics
Valdés, A. E., Irar, S., Majada, J. P., Rodríguez, A., Fernández, B., & Pagès, M. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2012.12.019 · Cited by 54
Cullin‐RING Ubiquitin Ligase Family in Plant Abiotic Stress PathwaysF
Guo, L., Nezames, C. D., Sheng, L., Deng, X., & Wei, N. (2012) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12019 · Cited by 54
The nuclear protein GmbZIP110 has transcription activation activity and plays important roles in the response to salinity stress in soybean
Xu, Z., Ali, Z., Xu, L., He, X., Huang, Y., Yi, J., Shao, H., Ma, H., & Zhang, D. (2016) · Scientific Reports · doi:10.1038/srep20366 · Cited by 54
Current evidence for a role of epigenetic mechanisms in response to ionizing radiation in an ecotoxicological context
Horemans, N., Spurgeon, D. J., Lecomte-Pradines, C., Saenen, E., Bradshaw, C., Oughton, D. H., Rasnaca, I., Kamstra, J. H., & Adam‐Guillermin, C. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.04.125 · Cited by 59
Non-coding RNAs: Functional roles in the regulation of stress response in Brassica crops
Waqas, A., Xia, Y., Li, R., Bai, G., Siddique, K. H. M., & Guo, P. (2019) · Genomics · doi:10.1016/j.ygeno.2019.08.011 · Cited by 55
Electrical Signals, Plant Tolerance to Actions of Stressors, and Programmed Cell Death: Is Interaction Possible?
Sukhova, E., & Sukhov, V. (2021) · Plants · doi:10.3390/plants10081704 · Cited by 53
Identification and characterization of salt-responsive microRNAs in Populus tomentosa by high-throughput sequencing
Ren, Y., Chen, L., Zhang, Y., Kang, X., Zhang, Z., & Wang, Y. (2012) · Biochimie · doi:10.1016/j.biochi.2012.10.025 · Cited by 53
Taking transgenic rice drought screening to the field
Gaudin, A. C. M., Henry, A., Sparks, A., & Slamet‐Loedin, I. H. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers313 · Cited by 53
De novo transcriptome analysis of Medicago falcata reveals novel insights about the mechanisms underlying abiotic stress-responsive pathway
Miao, Z., Xu, W. F., Li, D., Hu, X., Liu, J., Zhang, R., Tong, Z., Dong, J., Su, Z., Zhang, L., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-2019-x · Cited by 53
Genome-wide analysis of salt-responsive and novel microRNAs in Populus euphratica by deep sequencing
Si, J., Zhou, T., Bo, W., Xu, F., & Wu, R. (2014) · BMC Genetics · doi:10.1186/1471-2156-15-s1-s6 · Cited by 53
Physiological and Transcriptional Analyses Reveal Differential Phytohormone Responses to Boron Deficiency in Brassica napus Genotypes
Zhou, T., Hua, Y., Huang, Y., Ding, G., Shi, L. G., & Xu, F. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00221 · Cited by 53
Transgenic Approaches for Abiotic Stress Tolerance in Crop Plants
Wani, S. H., Sah, S. K., Hossain, M. A., Kumar, V., & Balachandran, S. M. (2016) · Springer eBooks · doi:10.1007/978-3-319-22518-0_10 · Cited by 54
GmWRKY49, a Salt-Responsive Nuclear Protein, Improved Root Length and Governed Better Salinity Tolerance in Transgenic Arabidopsis
Xu, Z., Raza, Q. S., Xu, L., He, X., Huang, Y., Yi, J., Zhang, D., Shao, H., Ma, H., & Ali, Z. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00809 · Cited by 53
Role of dehydrin-FK506-binding protein complex in enhancing drought tolerance through the ABA-mediated signaling pathway
Tiwari, P., Indoliya, Y., Singh, P. K., Singh, P. C., Chauhan, P. S., Pande, V., & Chakrabarty, D. (2018) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2018.10.031 · Cited by 53
Unlocking Triticeae genomics to sustainably feed the future
Mochida, K., & Shinozaki, K. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pct163 · Cited by 52
Self-citation
Overexpression of a wheat MYB transcription factor gene, TaMYB56-B, enhances tolerances to freezing and salt stresses in transgenic Arabidopsis
Zhang, L., Zhao, G., Xia, C., Jia, J., Liu, X., & Kong, X. (2012) · Gene · doi:10.1016/j.gene.2012.05.033 · Cited by 52
The ABA signal transduction mechanism in commercial crops: learning from Arabidopsis
Ben‐Ari, G. (2012) · Plant Cell Reports · doi:10.1007/s00299-012-1292-2 · Cited by 54
Elevated carbon dioxide decreases the adverse effects of higher temperature and drought stress by mitigating oxidative stress and improving water status in Arabidopsis thaliana
Gamar, M. I. A., Kisiała, A., Emery, R. J. N., Yeung, E. C.-T., Stone, S. L., & Qaderi, M. M. (2019) · Planta · doi:10.1007/s00425-019-03213-3 · Cited by 52
Overexpression of two R2R3-MYB genes from Scutellaria baicalensis induces phenylpropanoid accumulation and enhances oxidative stress resistance in transgenic tobacco
Qi, L.-J., Yang, J. T., Yuan, Y., Huang, L., & Chen, P. (2015) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2015.06.007 · Cited by 51
Prerequisites, performance and profits of transcriptional profiling the abiotic stress response
Kilian, J., Peschke, F., Berendzen, K. W., Harter, K., & Wanke, D. (2011) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2011.09.005 · Cited by 51
The barley stripe mosaic virus expression system reveals the wheat C2H2 zinc finger protein TaZFP1B as a key regulator of drought tolerance
Cheuk, A., Ouellet, F., & Houde, M. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-02355-x · Cited by 52
More than the sum of its parts – How to achieve a specific transcriptional response to abiotic stress
Vaahtera, L., & Brosché, M. (2010) · Plant Science · doi:10.1016/j.plantsci.2010.11.009 · Cited by 50
Integration of Genome-Scale Modeling and Transcript Profiling Reveals Metabolic Pathways Underlying Light and Temperature Acclimation in Arabidopsis
Töpfer, N., Caldana, C., Grimbs, S., Willmitzer, L., Fernie, A. R., & Nikoloski, Z. (2013) · The Plant Cell · doi:10.1105/tpc.112.108852 · Cited by 51
Comparative physiological and transcriptomic analyses provide integrated insight into osmotic, cold, and salt stress tolerance mechanisms in banana
Hu, W., Ding, Z., Tie, W., Yan, Y., Liu, Y., Wu, C., Liu, J., Wang, J., Peng, M., Xu, B., et al. (2017) · Scientific Reports · doi:10.1038/srep43007 · Cited by 50
The RING finger E3 ligases PIR1 and PIR2 mediate PP2CA degradation to enhance abscisic acid response in Arabidopsis
Baek, W., Lim, C. W., Luan, S., & Lee, S. C. (2019) · The Plant Journal · doi:10.1111/tpj.14507 · Cited by 51
Nanoforms of essential metals: from hormetic phytoeffects to agricultural potential
Kolbert, Z., Szőllősi, R., Rónavári, A., & Molnár, Á. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab547 · Cited by 51
Improving plant drought tolerance and growth under water limitation through combinatorial engineering of signalling networks
Schulz, P., Piepenburg, K., Lintermann, R., Herde, M., Schöttler, M. A., Schmidt, L. K., Ruf, S., Kudla, J., Romeis, T., & Bock, R. (2020) · Plant Biotechnology Journal · doi:10.1111/pbi.13441 · Cited by 49
Protein Phosphorylation Response to Abiotic Stress in Plants
Damaris, R. N., & Yang, P. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1625-3_2 · Cited by 49
Transcriptional Analysis of Drought-Induced Genes in the Roots of a Tolerant Genotype of the Common Bean (Phaseolus vulgaris L.)
Recchia, G. H., Caldas, D. G. G., Beraldo, A. L. A., Silva, M. D., & Tsai, S. M. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14047155 · Cited by 49
Transcriptome profiling reveals insights into the molecular mechanism of drought tolerance in sweetpotato
Zhu, H., Zhou, Y., Zhai, H., Shao-zhen, H. E., Zhao, N., & Liu, Q. (2019) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(18)61934-3 · Cited by 49
Bioinformatics Resources for Plant Abiotic Stress Responses: State of the Art and Opportunities in the Fast Evolving -Omics Era
Ambrosino, L., Colantuono, C., Diretto, G., Fiore, A., & Chiusano, M. L. (2020) · Plants · doi:10.3390/plants9050591 · Cited by 49
Chronic cement dust load induce novel damages in foliage and buds of Malus domestica
Shah, K., An, N., Ma, W., Ara, G., Ali, K., Каманова, С. Г., Zuo, X., Han, M., Ren, X., & Xing, L. (2020) · Scientific Reports · doi:10.1038/s41598-020-68902-6 · Cited by 49
Transcriptome and methylome changes in two contrasting mungbean genotypes in response to drought stress
Zhao, P., Ma, B., Cai, C., & Xu, J. (2022) · BMC Genomics · doi:10.1186/s12864-022-08315-z · Cited by 49
Histone chaperones in Arabidopsis and rice: genome-wide identification, phylogeny, architecture and transcriptional regulation
Tripathi, A. K., Singh, K., Pareek, A., & Singla-Pareek, S. L. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0414-8 · Cited by 47
Growth, physiology, and transcriptional analysis of Two contrasting Carex rigescens genotypes under Salt stress reveals salt-tolerance mechanisms
Li, M., Zhang, K., Sun, Y., Cui, H., Cao, S., Li, Y., & Xu, M. (2018) · Journal of Plant Physiology · doi:10.1016/j.jplph.2018.07.005 · Cited by 47
The integration of transcriptomic and transgenic analyses reveals the involvement of the SA response pathway in the defense of chrysanthemum against the necrotrophic fungus Alternaria sp.
Zhao, X., Song, L., Jiang, L., Zhu, Y., Gao, Q., Wang, D., Xie, J., Lv, M., Liu, P., & Li, M. (2020) · Horticulture Research · doi:10.1038/s41438-020-0297-1 · Cited by 47
Metabolomic Response of Calotropis procera Growing in the Desert to Changes in Water Availability
Ramadan, A. M., Sabir, J. S. M., Alakilli, S. Y. M., Shokry, A. M., Gadalla, N. O., Edris, S., Al-Kordy, M. A., Alzahrani, H. S., El-Domyati, F. M., Bahieldin, A., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087895 · Cited by 47
Evolutionary and expression analysis of CAMTA gene family in Nicotiana tabacum yielded insights into their origin, expansion and stress responses
Kakar, K. U., Nawaz, Z., Cui, Z., Cao, P., Jin, J., Shu, Q., & Ren, X. (2018) · Scientific Reports · doi:10.1038/s41598-018-28148-9 · Cited by 46
Heavy metal ATPase genes (HMAs) expression induced by endophytic bacteria, “AI001, and AI002” mediate cadmium translocation and phytoremediation
Ullah, I., Mateen, A., Ahmad, M. A., Munir, I., Iqbal, A., Al-Ghamdi, K. M. S., Al-Solami, H. M. A., & Siddiqui, M. F. (2021) · Environmental Pollution · doi:10.1016/j.envpol.2021.118508 · Cited by 47
Overexpression of a Malus baccata CBF transcription factor gene, MbCBF1, Increases cold and salinity tolerance in Arabidopsis thaliana
Liang, X., Luo, G., Li, W., Yao, A., Liu, W., Xie, L., Han, M., Li, X., & Han, D. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.10.012 · Cited by 46
Isolation and molecular characterization of a novel WIN1/SHN1 ethylene-responsive transcription factor TdSHN1 from durum wheat (Triticum turgidum. L. subsp. durum)
Djemal, R., & Khoudi, H. (2015) · PROTOPLASMA · doi:10.1007/s00709-015-0775-8 · Cited by 46
Expression analysis in response to drought stress in soybean: shedding light on the regulation of metabolic pathway genes
Guimarães-Dias, F., Neves‐Borges, A. C., Viana, A. A. B., Mesquita, R. O., Romano, E., Grossi‐de‐Sá, M. F., Nepomuceno, A. L., Loureiro, M., & Alves‐Ferreira, M. (2012) · Genetics and Molecular Biology · doi:10.1590/s1415-47572012000200004 · Cited by 46
Genotype by watering regime interaction in cultivated tomato: lessons from linkage mapping and gene expression
Albert, E., Gricourt, J., Bertin, N., Bonnefoi, J., Pateyron, S., Tamby, J., Bitton, F., & Causse, M. (2015) · Theoretical and Applied Genetics · doi:10.1007/s00122-015-2635-5 · Cited by 47
The yield difference between wild-type cotton and transgenic cotton that expresses IPT depends on when water-deficit stress is applied
Zhu, X., Sun, L., Kuppu, S., Hu, R., Mishra, N., Smith, J., Esmaeili, N., Herath, M., Gore, M. A., Payton, P., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-20944-7 · Cited by 46
Variations in Physiology and Multiple Bioactive Constituents under Salt Stress Provide Insight into the Quality Evaluation of Apocyni Veneti Folium
Chen, C., Wang, C., Liu, Z., Liu, X., Zou, L., Shi, J., Chen, S., Chen, J., & Tan, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103042 · Cited by 46
NADPH-dependent thioredoxin reductase A (NTRA) confers elevated tolerance to oxidative stress and drought
Cha, J., Kim, J. Y., Jung, I. J., Kim, M. R., Melencion, A., Alam, S. S., Yun, D., Lee, S. Y., Kim, M. G., & Kim, W. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.04.008 · Cited by 46
Deep sequencing-based characterization of transcriptome of Pyrus ussuriensis in response to cold stress
Yang, T., & Huang, X. (2018) · Gene · doi:10.1016/j.gene.2018.03.067 · Cited by 45
The intertwining of Zn-finger motifs and abiotic stress tolerance in plants: Current status and future prospects
Moulick, D., Bhutia, K. L., Sarkar, S., Roy, A., Mishra, U. N., Pramanick, B., Maitra, S., Shankar, T., Hazra, S., Skalický, M., et al. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1083960 · Cited by 47
Physiological and transcriptomic responses in the seed coat of field-grown soybean (Glycine max L. Merr.) to abiotic stress
Leisner, C. P., Yendrek, C. R., & Ainsworth, E. A. (2017) · BMC Plant Biology · doi:10.1186/s12870-017-1188-y · Cited by 45
Pseudomonas knackmussiiMLR6, a rhizospheric strain isolated from halophyte, enhances salt tolerance inArabidopsis thaliana
Rabhi, N. E. H., Silini, A., Cherif‐Silini, H., Yahiaoui, B., Lekired, A., Robineau, M., Esmaeel, Q., Jacquard, C., Vaillant‐Gaveau, N., Clément, C., et al. (2018) · Journal of Applied Microbiology · doi:10.1111/jam.14082 · Cited by 45
The Effect of Climate Change on Abiotic Plant Stress: A Review
Okoro, G. O., Boniface, O. O., Ngasoh, F. G., & Nicholas, N. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.82681 · Cited by 47
Wild relatives of plants as sources for the development of abiotic stress tolerance in plants
Hossain, A., Maitra, S., Pramanick, B., Bhutia, K. L., Ahmad, Z., Moulick, D., Syed, M. A., Shankar, T., Adeel, M., Hassan, M. M., et al. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85665-2.00011-x · Cited by 44
Common and distinct organ and stress responsive transcriptomic patterns in Oryza sativa and Arabidopsis thaliana
Narsai, R., Castleden, I. R., & Whelan, J. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-262 · Cited by 45
Effect of HbDHN1 and HbDHN2 Genes on Abiotic Stress Responses in Arabidopsis
Cao, Y., Xiang, X., Geng, M.-T., You, Q., & Huang, X. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00470 · Cited by 44
Y2SK2 and SK3 type dehydrins from Agapanthus praecox can improve plant stress tolerance and act as multifunctional protectants
Yang, Z., Sheng, J., Lv, K., Ren, L., & Zhang, D. (2019) · Plant Science · doi:10.1016/j.plantsci.2019.03.012 · Cited by 44
Transcriptomic profiling of sorghum leaves and roots responsive to drought stress at the seedling stage
Zhang, D., Zeng, T., Xu-yang, L. I. U., Gao, C., Li, Y., Li, C., Song, Y., Shi, Y., Wang, T., & Yu, L. I. (2019) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(18)62119-7 · Cited by 44
StMAPK3 controls oxidase activity, photosynthesis and stomatal aperture under salinity and osmosis stress in potato
Zhu, X., Zhang, N., Liu, X., Wang, S., Li, S., Yang, J., Wang, F., & Si, H. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.09.012 · Cited by 44
Multiple abiotic stress responsive rice cyclophilin: (OsCYP-25) mediates a wide range of cellular responses
Trivedi, D. K., Ansari, M. W., & Tuteja, N. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.25260 · Cited by 44
AtERF71/HRE2, an Arabidopsis AP2/ERF Transcription Factor Gene, Contains Both Positive and Negative Cis-Regulatory Elements in Its Promoter Region Involved in Hypoxia and Salt Stress Responses
Seok, H., Tran, H. T. L., Lee, S.-Y., & Moon, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105310 · Cited by 43
Biogenic nanoparticles and generation of abiotic stress-resilient plants: A new approach for sustainable agriculture
Chakraborty, S., Singh, A., & Roychoudhury, A. (2022) · Plant Stress · doi:10.1016/j.stress.2022.100117 · Cited by 43
Advances in Improving Adaptation of Common Bean and Brachiaria Forage Grasses to Abiotic Stresses in the Tropics
Rao, I. M. (2014) · Books in soils, plants, and the environment · doi:10.1201/b16675-49 · Cited by 43
Plant Metallothioneins
Joshi, R., Pareek, A., & Singla-Pareek, S. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-803158-2.00009-6 · Cited by 43
Overexpression of Arabidopsis AnnAt8 Alleviates Abiotic Stress in Transgenic Arabidopsis and Tobacco
Yadav, D., Ahmed, I., Shukla, P., Boyidi, P., & Kirti, P. B. (2016) · Plants · doi:10.3390/plants5020018 · Cited by 43
HyPRP1 Gene Suppressed by Multiple Stresses Plays a Negative Role in Abiotic Stress Tolerance in Tomato
Li, J., Ouyang, B., Wang, T., Luo, Z., Yang, C., Li, J., Sima, W., Zhang, J., & Ye, Z. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00967 · Cited by 43
Isolation and Functional Analysis of MbCBF2, a Malus baccata (L.) Borkh CBF Transcription Factor Gene, with Functions in Tolerance to Cold and Salt Stress in Transgenic Arabidopsis thaliana
Li, X., Liang, X., Li, W., Yao, A., Liu, W., Wang, Y., Yang, G., & Han, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179827 · Cited by 43
An emerging picture of the seed desiccome: confirmed regulators and newcomers identified using transcriptome comparison
Terrasson, E., Buitink, J., Righetti, K., Vu, B. L., Pelletier, S., Zinsmeister, J., Lalanne, D., & Leprince, O. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00497 · Cited by 43
Meta-Analysis of Expression of the Stress Tolerance Associated Genes and Uncover their Cis-Regulatory Elements in Rice (Oryza sativa L.)
Shariatipour, N., & Heidari, B. (2020) · The Open Bioinformatics Journal · doi:10.2174/1875036202013010039 · Cited by 42
ZmSNAC13, a maize NAC transcription factor conferring enhanced resistance to multiple abiotic stresses in transgenic Arabidopsis
Luo, P., Chen, Y., Rong, K., Lu, Y., Wang, N., Xu, Z., Pang, B., Zhou, D., Weng, J., Li, M., et al. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2021.11.032 · Cited by 42
An ATL78-Like RING-H2 Finger Protein Confers Abiotic Stress Tolerance through Interacting with RAV2 and CSN5B in Tomato
Song, J., Xing, Y., Munir, S., Yu, C., Song, L., Li, J., Wang, T., & Ye, Z. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01305 · Cited by 42
Comparative Transcriptome Analysis Reveals Molecular Defensive Mechanism of Arachis hypogaea in Response to Salt Stress
Zhang, H., Zhao, X., Sun, Q., Yan, C., Wang, J., Yuan, C., Li, C., Shan, S., & Liu, F. (2020) · International Journal of Genomics · doi:10.1155/2020/6524093 · Cited by 42
Down-Regulation of SlGRAS10 in Tomato Confers Abiotic Stress Tolerance
Habib, S., Lwin, Y. Y., & Li, N. (2021) · Genes · doi:10.3390/genes12050623 · Cited by 42
Drought and salt stress effects on biochemical changes and gene expression of photosystem II and catalase genes in selected onion cultivars
Chaudhry, U. K., Gökçe, Z. N. Ö., & Gökçe, A. F. (2021) · Biologia · doi:10.1007/s11756-021-00827-5 · Cited by 42
Drought Response in Forest Trees: From the Species to the Gene
Aranda, I., Gil‐Pelegrín, E., Gascó, A., Guevara, M. Á., Cano, F. J., de Miguel, M., Ramírez‐Valiente, J. A., Peguero‐Pina, J. J., Perdiguero, P., Soto, Á., et al. (2012) · Springer eBooks · doi:10.1007/978-3-642-32653-0_12 · Cited by 42
An insertional mutagenesis programme with an enhancer trap for the identification and tagging of genes involved in abiotic stress tolerance in the tomato wild-related species Solanum pennellii
Atarés, A., Moyano, E., Morales, B., Schleicher, P., García‐Abellán, J. O., Antón, T., García‐Sogo, B., Pérez‐Martín, F., Lozano, R., Pardo, F., et al. (2011) · Plant Cell Reports · doi:10.1007/s00299-011-1094-y · Cited by 42
Genome-Wide Analysis Reveals Dynamic Epigenomic Differences in Soybean Response to Low-Phosphorus Stress
Chu, S., Yu, K., Lv, L., Zhang, X., Sun, C., Liu, X., Zhang, J., Jiao, Y., & Zhang, D. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186817 · Cited by 41
Functions of two Malus hupehensis (Pamp.) Rehd. YTPs (MhYTP1 and MhYTP2) in biotic- and abiotic-stress responses
Wang, N., Guo, T., Sun, X., Jia, X., Wang, P., Shao, Y., Liang, B., Gong, X., & Ma, F. (2017) · Plant Science · doi:10.1016/j.plantsci.2017.05.002 · Cited by 41
Interference between arsenic‐induced toxicity and hypoxia
Kumar, V., Vogelsang, L., Seidel, T., Schmidt, R., Weber, M., Reichelt, M., Meyer, A. J., Clemens, S., Sharma, S. S., & Dietz, K. (2018) · Plant Cell & Environment · doi:10.1111/pce.13441 · Cited by 41
Overexpression of SlMBP22 in Tomato Affects Plant Growth and Enhances Tolerance to Drought Stress
Li, F., Chen, X., Zhou, S., Xie, Q., Wang, Y., Xiang, X., Hu, Z., & Chen, G. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110672 · Cited by 41
Understanding of the postgerminative development response to salinity and drought stresses in cucumber seeds by integrated proteomics and transcriptomics analysis
Du, C., Li, H., Liu, C., & Fan, H. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.104062 · Cited by 41

Authors: Hirayama, T., & Shinozaki, K.
Affiliations: RIKEN Advanced Science Institute (JP)
RIKEN Center for Sustainable Resource Science (JP)
Corresponding author: Shinozaki, Kazuo
ORCID: Hirayama, Takashi
Shinozaki, Kazuo
Venue: The Plant Journal
Publisher: Wiley
Published: 2010-03
Volume: 61
Issue: 6
Pages: 1041-1052
ISSN: 0960-7412 (ISSN-L)
1365-313X
DOI: 10.1111/j.1365-313x.2010.04124.x
OpenAlex: W2070923407
Cited by: 1,215
References: 123
Citations by year: 2026: 30 · 2025: 57 · 2024: 70 · 2023: 63 · 2022: 94 · 2021: 115 · 2020: 84 · 2019: 80 · 2018: 72 · 2017: 67 · 2016: 85 · 2015: 81 · 2014: 75 · 2013: 87 · 2012: 62
FWCI: 7.36
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 9 d)
Locations: The Plant Journal (publishedVersion)
PubMed (publishedVersion)
Funders: Ministry of Education, Culture, Sports, Science and Technology
Japan Society for the Promotion of Science
RIKEN
Advanced Science Institute
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: abiotic stress response, plant stress tolerance, gene expression profiling, cis-regulatory elements, alternative splicing, small RNA, chromatin regulation, multi-omics integration, crop stress tolerance, marker-assisted breeding
MeSH terms: Adaptation, Physiological, Plant Growth Regulators, Plants, RNA Processing, Post-Transcriptional, Stress, Physiological, Transcription, Genetic, Signal Transduction, Genes, Plant, Arabidopsis, Gene Expression Regulation, Plant, Genome, Plant, Genomics, RNA, Small Interfering, Epigenesis, Genetic, Metabolome

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

Research on plant abiotic stress responses in the post‐genome era: past, present and future

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