The DOI matches its Crossref record; 138 of the 138 references it cites were found in a registry or an index.
Surviving and thriving: How plants perceive and respond to temperature stress
Open accessAbstract
The dramatic temperature fluctuations spurred by climate change inhibit plant growth and threaten crop productivity. Unraveling how plants defend themselves against temperature-stress-induced cellular impairment is not only a crucial fundamental issue but is also of critical importance for agricultural sustainability and food security. Here, we review recent developments in elucidating the molecular mechanisms used by plants to sense and respond to cold and heat stress at multiple levels. We also describe the trade-off between plant growth and responses to high and low temperatures. Finally, we discuss possible strategies that could be used to engineer temperature-stress-tolerant, high-yielding crops.
Overview
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
Cites
Statistics
Verification
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The capsaicin receptor: a heat-activated ion channel in the pain pathway
Caterina, M. J., Schumacher, M. A., Tominaga, M., Rosen, T. A., Levine, J. D., & Julius, D. (1997) · Nature · doi:10.1038/39807 · Cited by 9,107
Abiotic Stress Signaling and Responses in Plants
Zhu, J.-K. (2016) · Cell · doi:10.1016/j.cell.2016.08.029 · Cited by 5,701
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
Thomashow, M. F. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.571 · Cited by 3,551
Temperature increase reduces global yields of major crops in four independent estimates
Zhao, C., Liu, B., Piao, S., Wang, X., Lobell, D. B., Huang, Y., Huang, M., Yao, Y., Bassu, S., Ciais, P., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701762114 · Cited by 3,311
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
Identification of a cold receptor reveals a general role for TRP channels in thermosensation
McKemy, D. D., Neuhausser, W. M., & Julius, D. (2002) · Nature · doi:10.1038/nature719 · Cited by 2,709
A TRP Channel that Senses Cold Stimuli and Menthol
Peier, A. M., Moqrich, A., Hergarden, A. C., Reeve, A. J., Andersson, D. A., Story, G. M., Earley, T. J., Dragoni, I., McIntyre, P., Bevan, S., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)00652-9 · Cited by 2,355
Gibberellin Metabolism and its Regulation
Yamaguchi, S. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092804 · Cited by 2,194
ROS as key players in plant stress signalling
Baxter, A., Mittler, R., & Suzuki, N. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert375 · Cited by 1,933
The Language of Calcium Signaling
Dodd, A. N., Kudla, J., & Sanders, D. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-070109-104628 · Cited by 1,317
Transcriptional Regulatory Network of Plant Heat Stress Response
Ohama, N., Sato, H., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2016.08.015 · Cited by 1,234
The Plant NADPH Oxidase RBOHD Mediates Rapid Systemic Signaling in Response to Diverse Stimuli
Miller, G., Schlauch, K., Tam, R., Cortes, D., Torres, M. A., Shulaev, V., Dangl, J. L., & Mittler, R. (2009) · Science Signaling · doi:10.1126/scisignal.2000448 · Cited by 1,141
Sakuma, Y., Maruyama, K., Osakabe, Y., Qin, F., Seki, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2006) · The Plant Cell · doi:10.1105/tpc.105.035881 · Cited by 1,129
The Combined Effect of Drought Stress and Heat Shock on Gene Expression in Tobacco
Rizhsky, L., Liang, H., & Mittler, R. (2002) · Plant Physiology · doi:10.1104/pp.006858 · Cited by 1,113
COLD1 Confers Chilling Tolerance in Rice
Ma, Y., Dai, X., Xu, Y., Luo, W., Zheng, X., Zeng, D., Pan, Y., Lin, X., Liu, H., Zhang, D., et al. (2015) · Cell · doi:10.1016/j.cell.2015.01.046 · Cited by 1,048
Energy balance and acclimation to light and cold
Huner, N. P. A., Öquist, G., & Sarhan, F. (1998) · Trends in Plant Science · doi:10.1016/s1360-1385(98)01248-5 · Cited by 1,009
Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity
Kadota, Y., Sklenář, J., Derbyshire, P., Stransfeld, L., Asai, S., Ntoukakis, V. E., Jones, J. D. G., Shirasu, K., Menke, F. L. H., Jones, A. M. E., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.02.021 · Cited by 987
Advances and challenges in uncovering cold tolerance regulatory mechanisms in plants
Ding, Y., Shi, Y., & Yang, S. (2019) · New Phytologist · doi:10.1111/nph.15696 · Cited by 969
Self-citationPhytochromes function as thermosensors in Arabidopsis
Jung, J.-H., Domijan, M., Klose, C., Biswas, S., Ezer, D., Gao, M., Khattak, A. K., Box, M. S., Charoensawan, V., Cortijo, S., et al. (2016) · Science · doi:10.1126/science.aaf6005 · Cited by 935
The ELF4–ELF3–LUX complex links the circadian clock to diurnal control of hypocotyl growth
Nusinow, D. A., Helfer, A., Hamilton, E. E., King, J. J., Imaizumi, T., Schultz, T. F., Farré, E. M., & Kay, S. A. (2011) · Nature · doi:10.1038/nature10182 · Cited by 907
Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3
Sung, S., & Amasino, R. M. (2004) · Nature · doi:10.1038/nature02195 · Cited by 896
Thriving under Stress: How Plants Balance Growth and the Stress Response
Zhang, H., Zhao, Y., & Zhu, J.-K. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.10.012 · Cited by 884
Knight, H., Trewavas, A. J., & Knight, M. R. (1996) · The Plant Cell · doi:10.1105/tpc.8.3.489 · Cited by 867
Phytochrome B integrates light and temperature signals in Arabidopsis
Legris, M., Klose, C., Burgie, E. S., Rojas, C. C. R., Neme, M., Hiltbrunner, A., Wigge, P. A., Schäfer, E., Vierstra, R. D., & Casal, J. J. (2016) · Science · doi:10.1126/science.aaf5656 · Cited by 867
Larkindale, J., Hall, J. D., Knight, M. R., & Vierling, E. (2005) · Plant Physiology · doi:10.1104/pp.105.062257 · Cited by 858
Molecular Regulation of CBF Signaling in Cold Acclimation
Shi, Y., Ding, Y., & Yang, S. (2018) · Trends in Plant Science · doi:10.1016/j.tplants.2018.04.002 · Cited by 856
Self-citationLi, L., Li, M., Yu, L., Zhou, Z., Liang, X., Liu, Z., Cai, G., Gao, L., Zhang, X., Wang, Y., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.02.009 · Cited by 845
Achard, P., Gong, F., Cheminant, S., Alioua, M., Hedden, P., & Genschik, P. (2008) · The Plant Cell · doi:10.1105/tpc.108.058941 · Cited by 827
Sakuma, Y., Maruyama, K., Qin, F., Osakabe, Y., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605639103 · Cited by 793
Molecular Regulation of Plant Responses to Environmental Temperatures
Ding, Y., Shi, Y., & Yang, S. (2020) · Molecular Plant · doi:10.1016/j.molp.2020.02.004 · Cited by 787
Self-citationDubiella, U., Seybold, H., Durian, G., Komander, E., Lassig, R., Witte, C., Schulze, W. X., & Romeis, T. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221294110 · Cited by 760
Shi, Y., Tian, S., Hou, L., Huang, X., Zhang, X., Guo, H., & Yang, S. (2012) · The Plant Cell · doi:10.1105/tpc.112.098640 · Cited by 709
Self-citationDoherty, C. J., Van Buskirk, H. A., Myers, S. J., & Thomashow, M. F. (2009) · The Plant Cell · doi:10.1105/tpc.108.063958 · Cited by 703
ABA receptor PYL9 promotes drought resistance and leaf senescence
Zhao, Y., Chan, Z., Gao, J., Xing, L., Cao, M., Yu, C., Hu, Y., You, J., Shi, H., Zhu, Y., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522840113 · Cited by 698
OST1 Kinase Modulates Freezing Tolerance by Enhancing ICE1 Stability in Arabidopsis
Ding, Y., Li, H., Zhang, X., Xie, Q., Gong, Z., & Yang, S. (2015) · Developmental Cell · doi:10.1016/j.devcel.2014.12.023 · Cited by 676
Self-citationQi, J., Song, C., Wang, B., Zhou, J., Kangasjärvi, J., Zhu, J., & Gong, Z. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12654 · Cited by 654
A prion-like domain in ELF3 functions as a thermosensor in Arabidopsis
Jung, J.-H., Barbosa, A. D., Hutin, S., Kumita, J. R., Gao, M., Derwort, D., Silva, C. S., Lai, X., Pierre, E., Geng, F., et al. (2020) · Nature · doi:10.1038/s41586-020-2644-7 · Cited by 638
Cold signaling in plants: Insights into mechanisms and regulation
Guo, X., Liu, D., & Chong, K. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12706 · Cited by 628
Protein kinases in plant responses to drought, salt, and cold stress
Chen, X., Ding, Y., Yang, Y., Song, C., Wang, B., Yang, S., Guo, Y., & Gong, Z. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13061 · Cited by 608
Self-citationReciprocal Regulation of the TOR Kinase and ABA Receptor Balances Plant Growth and Stress Response
Wang, P., Zhao, Y., Li, Z., Hsu, C.-C., Liu, X., Fu, L., Hou, Y.-J., Du, Y., Xie, S., Zhang, C., et al. (2018) · Molecular Cell · doi:10.1016/j.molcel.2017.12.002 · Cited by 591
Learning the Languages of the Chloroplast: Retrograde Signaling and Beyond
Chan, K. X., Phua, S. Y., Crisp, P., McQuinn, R., & Pogson, B. J. (2016) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043015-111854 · Cited by 582
Zhang, Y., Zhu, H., Zhang, Q., Li, M., Yan, M., Wang, R., Wang, L., Welti, R., Zhang, W., & Wang, X. (2009) · The Plant Cell · doi:10.1105/tpc.108.062992 · Cited by 580
Hydrogen peroxide sensor HPCA1 is an LRR receptor kinase in Arabidopsis
Wu, F., Chi, Y., Jiang, Z., Xu, Y., Xie, L., Huang, F., Wan, D., Ni, J., Yuan, F., Wu, X., et al. (2020) · Nature · doi:10.1038/s41586-020-2032-3 · Cited by 577
Endoplasmic Reticulum Stress Responses in Plants
Howell, S. H. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120053 · Cited by 560
Qin, F., Kakimoto, M., Sakuma, Y., Maruyama, K., Osakabe, Y., Tran, L. P., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03034.x · Cited by 524
Alternative splicing in plants – coming of age
Syed, N. H., Kalyna, M., Marquez, Y., Barta, A., & Brown, J. W. S. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.06.001 · Cited by 509
MAP Kinase Cascades Regulate the Cold Response by Modulating ICE1 Protein Stability
Zhao, C., Wang, P., Si, T., Hsu, C.-C., Wang, L., Zayed, O., Yu, Z., Zhu, Y., Dong, J., Tao, W. A., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.09.024 · Cited by 498
Li, H., Ding, Y., Shi, Y., Zhang, X., Zhang, S., Gong, Z., & Yang, S. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.09.025 · Cited by 489
Self-citationJia, Y., Ding, Y., Shi, Y., Zhang, X., Gong, Z., & Yang, S. (2016) · New Phytologist · doi:10.1111/nph.14088 · Cited by 481
Self-citationDeng, Y., Humbert, S., Liu, J.-X., Srivastava, R., Rothstein, S. J., & Howell, S. H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102117108 · Cited by 473
Improvement of stress tolerance of wheat and barley by modulation of expression of DREB/CBF factors
Morran, S., Eini, O., Pyvovarenko, T., Parent, B., Singh, R., Ismagul, A., Eliby, S., Shirley, N., Langridge, P., & Lopato, S. (2011) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2010.00547.x · Cited by 462
Liu, J.-X., Srivastava, R., Che, P., & Howell, S. H. (2008) · The Plant Cell · doi:10.1105/tpc.106.050021 · Cited by 456
Mori, I. C., & Schroeder, J. I. (2004) · Plant Physiology · doi:10.1104/pp.104.042069 · Cited by 425
Liu, Z., Jia, Y., Ding, Y., Shi, Y., Li, Z., Guo, Y., Gong, Z., & Yang, S. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.02.016 · Cited by 416
Self-citationLi, X.-M., Chao, D.-Y., Wu, Y., Huang, X., Chen, K., Cui, L.-G., Su, L., Ye, W.-W., Chen, H., Chen, H.-C., et al. (2015) · Nature Genetics · doi:10.1038/ng.3305 · Cited by 402
Jeon, J., Kim, N. Y., Kim, S., Kang, N. Y., Novák, O., Ku, S.-J., Cho, C., Lee, D. J., Lee, E.-J., Strnad, M., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.096644 · Cited by 379
Suzuki, N., Miller, G., Salazar, C., Mondal, H. A., Shulaev, E., Cortes, D. F., Shuman, J. L., Luo, X., Shah, J., Schlauch, K., et al. (2013) · The Plant Cell · doi:10.1105/tpc.113.114595 · Cited by 375
Hormonal control of cold stress responses in plants
Eremina, M., Rozhon, W., & Poppenberger, B. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2089-6 · Cited by 370
ROS signaling loops — production, perception, regulation
Wrzaczek, M., Brosché, M., & Kangasjärvi, J. (2013) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2013.07.002 · Cited by 357
Oxidative Stress-Induced Calcium Signaling in Arabidopsis
Rentel, M. C., & Knight, M. R. (2004) · Plant Physiology · doi:10.1104/pp.104.042663 · Cited by 351
Liu, X. L. (2001) · THE PLANT CELL ONLINE · doi:10.1105/tpc.13.6.1293 · Cited by 334
Hormonal regulation of temperature‐induced growth in Arabidopsis
Stavang, J. A., Gallego‐Bartolomé, J., Gómez, M. D., Yoshida, S., Asami, T., Olsen, J. E., García‐Martínez, J. L., Alabadí, D., & Blázquez, M. A. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03983.x · Cited by 331
Mapping of QTLs associated with cold tolerance during the vegetative stage in rice
Andaya, V. C. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erg243 · Cited by 324
Rapid, Long-Distance Electrical and Calcium Signaling in Plants
Choi, W.-G., Hilleary, R., Swanson, S. J., Kim, S.-H., & Gilroy, S. (2016) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043015-112130 · Cited by 312
Seo, P. J., Park, M.-J., Lim, M.-H., Kim, S.-G., Lee, M., Baldwin, I. T., & Park, C.-M. (2012) · The Plant Cell · doi:10.1105/tpc.112.098723 · Cited by 293
Early selection of bZIP73 facilitated adaptation of japonica rice to cold climates
Liu, C., Ou, S., Mao, B., Tang, J., Wang, W., Wang, H., Cao, S., Schläppi, M. R., Zhao, B., Xiao, G., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05753-w · Cited by 278
The pathway for perception and transduction of low-temperature signals in Synechocystis
Suzuki, I. (2000) · The EMBO Journal · doi:10.1093/emboj/19.6.1327 · Cited by 275
Gao, H., Brandizzi, F., Benning, C., & Larkin, R. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808463105 · Cited by 273
Jiang, B., Shi, Y., Peng, Y., Jia, Y., Yan, Y., Dong, X., Li, H., Dong, J., Li, J., Gong, Z., et al. (2020) · Molecular Plant · doi:10.1016/j.molp.2020.04.006 · Cited by 255
Self-citationKidokoro, S., Yoneda, K., Takasaki, H., Takahashi, F., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2017) · The Plant Cell · doi:10.1105/tpc.16.00669 · Cited by 238
CYCLIC NUCLEOTIDE-GATED ION CHANNELs 14 and 16 Promote Tolerance to Heat and Chilling in Rice
Cui, Y., Lu, S., Li, Z., Cheng, J., Hu, P., Zhu, T., Wang, X., Jin, M., Wang, X., Li, L., et al. (2020) · Plant Physiology · doi:10.1104/pp.20.00591 · Cited by 238
Insights into the regulation of C‐repeat binding factors in plant cold signaling
Liu, J., Shi, Y., & Yang, S. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12657 · Cited by 237
Self-citationDephosphorylated SRp38 acts as a splicing repressor in response to heat shock
Shin, C., Feng, Y., & Manley, J. L. (2004) · Nature · doi:10.1038/nature02288 · Cited by 231
Yang, T., Chaudhuri, S., Yang, L., Du, L., & Poovaiah, B. W. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.035659 · Cited by 229
Yang, Z.-T., Wang, M.-J., Sun, L., Lu, S.-J., Bi, D.-L., Sun, L., Song, Z.-T., Zhang, S.-S., Zhou, S.-F., & Liu, J.-X. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004243 · Cited by 225
A membrane‐associated NAC transcription factor OsNTL3 is involved in thermotolerance in rice
Liu, X., Lyu, Y., Yang, W., Yang, Z., Lu, S., & Liu, J. (2020) · Plant Biotechnology Journal · doi:10.1111/pbi.13297 · Cited by 225
Ye, K., Li, H., Ding, Y., Shi, Y., Song, C.-P., Gong, Z., & Yang, S. (2019) · The Plant Cell · doi:10.1105/tpc.19.00058 · Cited by 224
Self-citationTranscriptional activation and phosphorylation of OsCNGC9 confer enhanced chilling tolerance in rice
Wang, J., Ren, Y., Liu, X., Luo, S., Zhang, X., Liu, X., Lin, Q., Zhu, S., Wan, H., Yang, Y., et al. (2021) · Molecular Plant · doi:10.1016/j.molp.2020.11.022 · Cited by 221
Polisensky, D. H., & Braam, J. (1996) · Plant Physiology · doi:10.1104/pp.111.4.1271 · Cited by 211
Lee, B.-H., Kapoor, A., Zhu, J., & Zhu, J.-K. (2006) · The Plant Cell · doi:10.1105/tpc.106.042184 · Cited by 209
Liu, Q., Ding, Y., Shi, Y., Ma, L., Wang, Y., Song, C., Wilkins, K. A., Davies, J. M., Knight, H., Knight, M. R., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020104559 · Cited by 207
Self-citationDirect Sensing of Heat and Oxidation by Drosophila Heat Shock Transcription Factor
Zhong, M., Orosz, A., & Wu, C. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80118-5 · Cited by 203
Dong, P., Xiong, F., Que, Y., Wang, K., Yu, L., Li, Z., & Ren, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00677 · Cited by 199
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 188
Structural plasticity and catalysis regulation of a thermosensor histidine kinase
Albanesi, D., Martín, M., Trajtenberg, F., Mansilla, M. C., Haouz, A., Alzari, P. M., de Mendoza, D., & Buschiazzo, A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906699106 · Cited by 186
Pino, M., Skinner, J. S., Park, E., Jeknić, Z., Hayes, P. M., Thomashow, M. F., & Chen, T. H. H. (2007) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2007.00269.x · Cited by 181
Xie (2021) · doi:10.1111/jipb.13161 · Cited by 180
A Sacrifice-for-Survival Mechanism Protects Root Stem Cell Niche from Chilling Stress
Hong, J. H., Savina, M., Du, J., Devendran, A., Kannivadi Ramakanth, K., Tian, X., Sim, W. S., Mironova, V. V., & Xu, J. (2017) · Cell · doi:10.1016/j.cell.2017.06.002 · Cited by 180
The bZIP 73 transcription factor controls rice cold tolerance at the reproductive stage
Liu, C., Schläppi, M. R., Mao, B., Wang, W., Wang, A., & Chu, C. (2019) · Plant Biotechnology Journal · doi:10.1111/pbi.13104 · Cited by 180
OST 1‐mediated BTF 3L phosphorylation positively regulates CBF s during plant cold responses
Ding, Y., Jia, Y., Shi, Y., Zhang, X., Song, C., Gong, Z., & Yang, S. (2018) · The EMBO Journal · doi:10.15252/embj.201798228 · Cited by 179
Self-citationHofmann, S., Cherkasova, V., Bankhead, P., Bukau, B., & Stoecklin, G. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-04-0296 · Cited by 178
Zhang, S.-S., Yang, H., Ding, L., Song, Z.-T., Ma, H., Chang, F., & Liu, J.-X. (2017) · The Plant Cell · doi:10.1105/tpc.16.00916 · Cited by 178
Molecular mechanism of thermosensory function of human heat shock transcription factor Hsf1
Hentze, N., Breton, L. L., Wiesner, J., Kempf, G., & Mayer, M. P. (2016) · eLife · doi:10.7554/elife.11576 · Cited by 177
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 177
Thermopriming triggers splicing memory in Arabidopsis
Ling, Y., Serrano, N., Gao, G., Atia, M., Mokhtar, M., Woo, Y. H., Bazin, J., Veluchamy, A., Benhamed, M., Crespi, M., et al. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery062 · Cited by 175
Srivastava, R., Deng, Y., Shah, S., Rao, A. G., & Howell, S. H. (2013) · The Plant Cell · doi:10.1105/tpc.113.110684 · Cited by 170
Phototropin perceives temperature based on the lifetime of its photoactivated state
Fujii, Y., Tanaka, H., Konno, N., Ogasawara, Y., Hamashima, N., Tamura, S., Hasegawa, S., Hayasaki, Y., Okajima, K., & Kodama, Y. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1704462114 · Cited by 170
Natural variation in a type-A response regulator confers maize chilling tolerance
Zeng, R., Li, Z., Shi, Y., Fu, D., Yin, P., Cheng, J., Jiang, C., & Yang, S. (2021) · Nature Communications · doi:10.1038/s41467-021-25001-y · Cited by 169
Self-citationThe CRY2–COP1–HY5–BBX7/8 module regulates blue light-dependent cold acclimation in Arabidopsis
Li, Y., Shi, Y., Li, M., Fu, D., Wu, S., Li, J., Gong, Z., Liu, H., & Yang, S. (2021) · The Plant Cell · doi:10.1093/plcell/koab215 · Cited by 168
Self-citationLi, Z., Tang, J., Srivastava, R., Bassham, D. C., & Howell, S. H. (2020) · The Plant Cell · doi:10.1105/tpc.20.00260 · Cited by 166
Emerging Roles for Phase Separation in Plants
Emenecker, R. J., Holehouse, A. S., & Strader, L. C. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.09.010 · Cited by 162
COP1 destabilizes DELLA proteins in Arabidopsis
Blanco‐Touriñán, N., Legris, M., Minguet, E. G., Rojas, C. C., Nohales, M. A., Iniesto, E., García-León, M., Pacín, M., Heucken, N., Blomeier, T., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1907969117 · Cited by 158
Natural variations of SLG1 confer high-temperature tolerance in indica rice
Xu, Y., Zhang, L., Ou, S., Wang, R., Wang, Y., Chu, C., & Yao, S. (2020) · Nature Communications · doi:10.1038/s41467-020-19320-9 · Cited by 158
Qu, Y., Sakoda, K., Fukayama, H., Kondo, E., Suzuki, Y., Makino, A., Terashima, I., & Yamori, W. (2021) · Plant Cell & Environment · doi:10.1111/pce.14051 · Cited by 158
Calcium/calmodulin-regulated receptor-like kinase CRLK1 interacts with MEKK1 in plants
Yang, T., Ali, G. S., Yang, L., Du, L., Reddy, A. S. N., & Poovaiah, B. W. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.8.12225 · Cited by 151
Pre-mRNA alternative splicing as a modulator for heat stress response in plants
Ling, Y., Mahfouz, M. M., & Zhou, S. (2021) · Trends in Plant Science · doi:10.1016/j.tplants.2021.07.008 · Cited by 151
Molecular mechanisms of heat shock factor 1 regulation
Kmiecik, S. W., & Mayer, M. P. (2021) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2021.10.004 · Cited by 151
Mori, K., Renhu, N., Naito, M., Nakamura, A., Shiba, H., Yamamoto, T., Suzaki, T., Iida, H., & Miura, K. (2018) · Scientific Reports · doi:10.1038/s41598-017-17483-y · Cited by 149
EGR2 phosphatase regulates OST1 kinase activity and freezing tolerance in Arabidopsis
Ding, Y., Lv, J., Shi, Y., Gao, J., Hua, J., Song, C., Gong, Z., & Yang, S. (2018) · The EMBO Journal · doi:10.15252/embj.201899819 · Cited by 148
Self-citationSharwood, R. E., Ghannoum, O., Kapralov, M. V., Gunn, L. H., & Whitney, S. M. (2016) · Nature Plants · doi:10.1038/nplants.2016.186 · Cited by 141
Lu, S., Yang, Z., Sun, L. V., Sun, L., Song, Z., & Liu, J. (2011) · Molecular Plant · doi:10.1093/mp/ssr115 · Cited by 138
Yang, Z., Lu, S., Wang, M., Bi, D., Sun, L. V., Zhou, S., Song, Z., & Liu, J. (2014) · The Plant Journal · doi:10.1111/tpj.12604 · Cited by 135
Nawkar, G. M., Kang, C. H., Maibam, P., Park, J. H., Jung, Y. J., Chae, H. B., Chi, Y. H., Jung, I. J., Kim, W. Y., Yun, D., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1609844114 · Cited by 128
Wang, L., Li, H., Zhao, C., Li, S., Kong, L., Wu, W., Kong, W., Liú, Y., Wei, Y., Zhu, J., et al. (2016) · Plant Cell & Environment · doi:10.1111/pce.12826 · Cited by 124
RCD1–DREB2A interaction in leaf senescence and stress responses in Arabidopsis thaliana
Vainonen, J. P., Jaspers, P., Wrzaczek, M., Lamminmäki, A., Reddy, R. A., Vaahtera, L., Brosché, M., & Kangasjärvi, J. (2011) · Biochemical Journal · doi:10.1042/bj20111739 · Cited by 119
Temperature-dependent growth contributes to long-term cold sensing
Zhao, Y., Antoniou-Kourounioti, R. L., Calder, G. M., Dean, C., & Howard, M. (2020) · Nature · doi:10.1038/s41586-020-2485-4 · Cited by 116
Chloroplast-to-Nucleus Signaling Regulates MicroRNA Biogenesis in Arabidopsis
Fang, X., Zhao, G., Zhang, S., Li, Y., Gu, H., Li, Y., Zhao, Q. L., & Qi, Y. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.11.046 · Cited by 115
Seo, P. J., Park, M., & Park, C. (2013) · Planta · doi:10.1007/s00425-013-1882-4 · Cited by 105
Wang, X., Ma, X., Wang, H., Li, B., Clark, G., Guo, Y., Roux, S., Sun, D., & Tang, W. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m114.042697 · Cited by 97
Liu, Y., Zhang, C., Chen, J., Guo, L., Li, X., Li, W., Yu, Z., Deng, J.-S., Zhang, P., Zhang, K., et al. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.12.013 · Cited by 96
Hu, Y., Mesihović, A., Jiménez‐Gómez, J. M., Röth, S., Gebhardt, P., Bublak, D., Bovy, A. G., Scharf, K., Schleiff, E., & Fragkostefanakis, S. (2019) · New Phytologist · doi:10.1111/nph.16221 · Cited by 95
Findlay, K. M. W., & Jenkins, G. I. (2016) · Plant Cell & Environment · doi:10.1111/pce.12724 · Cited by 94
Plant target of rapamycin signaling network: Complexes, conservations, and specificities
Liu, Y., & Xiong, Y. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13212 · Cited by 88
Antoniou-Kourounioti, R. L., Hepworth, J., Heckmann, A., Duncan, S. H., Questa, J. I., Rosa, S., Säll, T., Holm, S., Dean, C., & Howard, M. (2018) · Cell Systems · doi:10.1016/j.cels.2018.10.011 · Cited by 77
Integration of light and temperature signaling pathways in plants
Qi, L., Shi, Y., Terzaghi, W., Yang, S., & Li, J. (2022) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13216 · Cited by 74
Self-citationSrivastava, R., Chen, Y., Deng, Y., Brandizzí, F., & Howell, S. H. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04943.x · Cited by 70
Chu, M., Li, J., Zhang, J., Shen, S., Li, C., Gao, Y., & Zhang, S. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery278 · Cited by 67
Cybulski, L. E., Ballering, J., Moussatova, A., Inda, M. E., Vazquez, D. B., Wassenaar, T. A., de Mendoza, D., Tieleman, D. P., & Killian, J. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422446112 · Cited by 66
Li, S., Yu, X., Cheng, Z., Zeng, C., Li, W., Zhang, L., & Peng, M. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz444 · Cited by 54
Lv, J., Liu, J., Ming, Y., Shi, Y., Song, C., Gong, Z., Yang, S., & Ding, Y. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13100 · Cited by 52
Self-citationPerception and transduction of low-temperature signals to induce desaturation of fatty acids
Suzuki, I., Los, D. A., & Murata, N. (2000) · Biochemical Society Transactions · doi:10.1042/bst0280628 · Cited by 48
Červený, J., Sinetova, M. A., Zavřel, T., & Los, D. A. (2015) · Life · doi:10.3390/life5010676 · Cited by 46
STABILIZED1 Modulates Pre-mRNA Splicing for Thermotolerance
Kim, G.-D., Cho, Y.-H., Lee, B., & Yoo, S.-D. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01928 · Cited by 45
Systemic signaling contributes to the unfolded protein response of the plant endoplasmic reticulum
Lai, Y.-S., Stefano, G., Zemelis‐Durfee, S., Ruberti, C., Gibbons, L., & Brandizzí, F. (2018) · Nature Communications · doi:10.1038/s41467-018-06289-9 · Cited by 37
SPLICING FACTOR1 Is Important in Chloroplast Development under Cold Stress
Zhu, Y., Wu, W., Shao, W., Chen, J., Shi, X., Ma, X., Xu, Y.-Z., Huang, W., & Huang, J. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00706 · Cited by 23
Wang, B., Chai, H., Zhong, Y., Shen, Y., Yang, W., Chen, J., Xin, Z., & Shi, H. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz523 · Cited by 20
Recognition of CCA1 alternative protein isoforms during temperature acclimation
Zhang, S., Liu, H., Li, Y., Li, X., Wang, L., Xu, X., & Xie, Q. (2021) · Plant Cell Reports · doi:10.1007/s00299-020-02644-7 · Cited by 19
Zhang, X., Wang, W., Kang, X., & Zhao, L. (2019) · Plant Growth Regulation · doi:10.1007/s10725-019-00552-9 · Cited by 18
Metadata
- Authors
- Ding, Y., & Yang, S.
- Venue
- Developmental Cell
- Publisher
- Elsevier BV
- Published
- 2022-04
- Volume
- 57
- Issue
- 8
- Pages
- 947-958
- ISSN
- 1534-5807 (ISSN-L)
- OpenAlex
- W4223462476
- Cited by
- 396
- References
- 138
- FWCI
- 38.49
- Type
- journal article
- Language
- en
- Open access
- bronze
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.