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OsWRKY12 negatively regulates the drought-stress tolerance and secondary cell wall biosynthesis by targeting different downstream transcription factor genes in rice
Open accessAbstract
With the increasing occurrence of global warming, drought is becoming a major constraint for plant growth and crop yield. Plant cell walls experience continuous changes during the growth, development, and in responding to stressful conditions. The plant WRKYs play pivotal roles in regulating the secondary cell wall (SCW) biosynthesis and helping plant defend against abiotic stresses. qRT-PCR evidence showed that OsWRKY12 was affected by drought and ABA treatments. Over-expression of OsWRKY12 decreased the drought tolerance of the rice transgenics at the germination stage and the seedling stage. The transcription levels of drought-stress-associated genes as well as those genes participating in the ABA biosynthesis and signaling were significantly different compared to the wild type (WT). Our results also showed that less lignin and cellulose were deposited in the OsWRKY12-overexpressors, and heterogenous expression of OsWRKY12 in atwrky12 could lower the increased lignin and cellulose contents, as well as the improved PEG-stress tolerance, to a similar level as the WT. qRT-PCR results indicated that the transcription levels of all the genes related to lignin and cellulose biosynthesis were significantly decreased in the rice transgenics than the WT. Further evidence from yeast one-hybrid assay and the dual-luciferase reporter system suggested that OsWRKY12 could bind to promoters of OsABI5 (the critical component of the ABA signaling pathway) and OsSWN3/OsSWN7 (the key positive regulators in the rice SCW thickening), and hence repressing their expression. In conclusion, OsWRKY12 mediates the crosstalk between SCW biosynthesis and plant stress tolerance by binding to the promoters of different downstream genes.
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“In rice, OsWRKY12 functions as a negative regulator by repressing genes involved in abscisic acid (ABA) signaling and secondary cell wall biosynthesis, thereby decreasing drought tolerance (Jia et al., 2024).”
From Emerging applications of gene editing technologies for the development of climate-resilient crops (2025) · cites this paper as Jia et al., 2024
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Cites
Rushton, P. J., Somssich, I. E., Ringler, P., & Shen, Q. J. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.02.006 · Cited by 2,759
The FERONIA Receptor Kinase Maintains Cell-Wall Integrity during Salt Stress through Ca2+ Signaling
Feng, W., Kita, D., Peaucelle, A., Cartwright, H. N., Doan, V., Duan, Q., Liu, M.-C. J., Maman, J., Steinhorst, L., Schmitz-Thom, I., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.023 · Cited by 770
Plant cell wall‐mediated immunity: cell wall changes trigger disease resistance responses
Bacete, L., Mélida, H., Miedes, E., & Molina, A. (2017) · The Plant Journal · doi:10.1111/tpj.13807 · Cited by 662
Wu, X., Shiroto, Y., Kishitani, S., Ito, Y., & Toriyama, K. (2008) · Plant Cell Reports · doi:10.1007/s00299-008-0614-x · Cited by 542
Characterization of Stress-Responsive CIPK Genes in Rice for Stress Tolerance Improvement
Xiang, Y., Huang, Y., & Xiong, L. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.101295 · Cited by 506
Wang, H., Avcı, U., Nakashima, J., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016436107 · Cited by 406
Cell wall integrity maintenance during plant development and interaction with the environment
Vaahtera, L., Schulz, J., & Hamann, T. (2019) · Nature Plants · doi:10.1038/s41477-019-0502-0 · Cited by 391
Transcriptional Factors Regulate Plant Stress Responses Through Mediating Secondary Metabolism
Meraj, T. A., Fu, J., Raza, M. A., Zhu, C., Shen, Q., Xu, D., & Wang, Q. (2020) · Genes · doi:10.3390/genes11040346 · Cited by 374
Zhong, R., Lee, C., McCarthy, R. L., et al. (2011) · Plant and Cell Physiology · doi:10.1093/pcp/pcr123 · Cited by 348
A Gibberellin-Mediated DELLA-NAC Signaling Cascade Regulates Cellulose Synthesis in Rice
Huang, D., Wang, S., Zhang, B., et al. (2015) · The Plant Cell · doi:10.1105/tpc.15.00015 · Cited by 335
Structural features and regulation of lignin deposited upon biotic and abiotic stresses
Cesarino, I. (2019) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2018.12.012 · Cited by 331
Secondary cell wall biosynthesis.
Zhong, R., Cui, D., & Ye, Z.-H. (2018) · New Phytologist · doi:10.1111/nph.15537 · Cited by 315
A wall with integrity: surveillance and maintenance of the plant cell wall under stress
Rui, Y., & Dinneny, J. R. (2019) · New Phytologist · doi:10.1111/nph.16166 · Cited by 315
OsWRKY30 is activated by MAP kinases to confer drought tolerance in rice
Shen, H., Liu, C., Zhang, Y., Meng, X.-P., Zhou, X. E., Chu, C., & Wang, X. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9941-y · Cited by 263
The evolution of WRKY transcription factors
Rinerson, C. I., Rabara, R., Tripathi, P., Shen, Q. J., & Rushton, P. J. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0456-y · Cited by 263
Khoso, M. A., Hussain, A., Ritonga, F. N., Ali, Q., Channa, M. M., Alshegaihi, R. M., Meng, Q., Ali, M., Zaman, W., Dad, R., et al. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1039329 · Cited by 249
Peng, L., Hocart, C. H., Redmond, J. W., & Williamson, R. E. (2000) · Planta · doi:10.1007/s004250000301 · Cited by 228
Induced over-expression of the transcription factor OsDREB2A improves drought tolerance in rice
Cui, M., Zhang, W., Zhang, Q., Xu, Z., Zhu, Z., Duan, F., & Wu, R. J. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.09.012 · Cited by 205
Lim, C., Kang, K., Shim, Y., Yoo, S., & Paek, N. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab492 · Cited by 201
ROS interplay between plant growth and stress biology: Challenges and future perspectives
Ali, S., Tyagi, A., & Bae, H. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.108032 · Cited by 184
Fungal elicitor-mediated responses in pine cell cultures
Campbell, M. M., & Ellis, B. (1992) · Planta · doi:10.1007/bf00195322 · Cited by 169
Rice WRKY11 Plays a Role in Pathogen Defense and Drought Tolerance
Lee, H., Cha, J., Choi, C., et al. (2018) · Rice · doi:10.1186/s12284-018-0199-0 · Cited by 142
Li, Y., Zhou, J., Li, Z., Qiao, J., Quan, R., Wang, J., Huang, R., & Qin, H. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac125 · Cited by 136
Li, Y., Han, S., Sun, X., et al. (2022) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13414 · Cited by 128
BpNAC012 Positively Regulates Abiotic Stress Responses and Secondary Wall Biosynthesis
Hu, P., Zhang, K., & Yang, C. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.01167 · Cited by 126
CEF1/OsMYB103L is involved in GA-mediated regulation of secondary wall biosynthesis in rice
Ye, Y., Liu, B., Zhao, M., et al. (2015) · Plant Molecular Biology · doi:10.1007/s11103-015-0376-0 · Cited by 124
Xie, W., Ke, Y., Cao, J., et al. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab400 · Cited by 116
Yang, L. C., Zhao, X., Yang, F., et al. (2016) · Scientific Reports · doi:10.1038/srep18643 · Cited by 100
Seven plant capacities to adapt to abiotic stress
Munns, R., & Millar, A. H. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad179 · Cited by 100
Yu, Y., Hu, R., Wang, H., Cao, Y., He, G. Q., Fu, C., & Zhou, G. (2013) · Plant Science · doi:10.1016/j.plantsci.2013.07.010 · Cited by 81
Li, X., Tang, Y. J., Zhou, C., Zhang, L., & Lv, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041321 · Cited by 63
Wheat WRKY transcription factor TaWRKY24 confers drought and salt tolerance in transgenic plants
Yu, Y., He, L., & Wu, Y. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.108137 · Cited by 63
Cai, W., Yang, Y., Wang, W., Guo, G., Liu, W., & Bi, C. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.01.008 · Cited by 60
Self-citationTang, Y., Lu, L., Huang, X., et al. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac507 · Cited by 60
Liu, Y., Wang, B., Li, J., et al. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2021.10.006 · Cited by 52
Double knockout of OsWRKY36 and OsWRKY102 boosts lignification with altering culm morphology of rice
Miyamoto, T., Takada, R., Tobimatsu, Y., 鈴木史朗, Yamamura, M., Osakabe, K., Osakabe, Y., Sakamoto, M., & Umezawa, T. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110466 · Cited by 45
OsWRKY114 Negatively Regulates Drought Tolerance by Restricting Stomatal Closure in Rice
Song, G., Son, S., Lee, K. S., et al. (2022) · Plants · doi:10.3390/plants11151938 · Cited by 45
OsTMF attenuates cold tolerance by affecting cell wall properties in rice
Xu, Y., Hu, D., Hou, X., et al. (2020) · New Phytologist · doi:10.1111/nph.16549 · Cited by 44
Ye, Y., Wang, S., Wu, K., Ren, Y., Jiang, H., Chen, J., Tao, L., Fu, X., Liu, B., & Wu, Y. (2021) · Rice · doi:10.1186/s12284-021-00457-0 · Cited by 42
Li, J., Meng, L., Ren, S., et al. (2023) · Plants · doi:10.3390/plants12173166 · Cited by 34
Wilschut, R. A., Long, J. R. D., Geisen, S., Hannula, S. E., Quist, C. W., Snoek, B. L., Steinauer, K., Wubs, E. R. J., Yang, Q., & Thakur, M. P. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2022.1178 · Cited by 27
OsWRKY76 positively regulates drought stress via OsbHLH148-mediated jasmonate signaling in rice
Zhang, M., Zhao, R., Huang, K., et al. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1168723 · Cited by 25
Feng, X., Abubakar, A. S., Yu, C., et al. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.812988 · Cited by 17
Jia, S., Liu, X., Li, X., Sun, C., Cao, X., Liu, W., Guo, G., & Bi, C. (2023) · Journal of Plant Physiology · doi:10.1016/j.jplph.2023.153997 · Cited by 9
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Research works printed but not linked: 1
- Jin, 2023, Cotton GhNAC4 promotes drought tolerance by regulating secondary cell wall biosynthesis and ribosomal protein homeostasis, Plant J.
Cited by
Sorted by citations
Emerging applications of gene editing technologies for the development of climate-resilient crops
Chavhan, R. L., Jaybhaye, S. G., Hinge, V. R., Deshmukh, A. S., Shaikh, U. S., Jadhav, P. K., Kadam, U. S., & Hong, J. C. (2025) · Frontiers in Genome Editing · doi:10.3389/fgeed.2025.1524767 · Cited by 55
Metadata
- Authors
- Jia, S., Wang, C., Sun, W., Yan, X., Wang, W., Xu, B., Guo, G., & Bi, C.
- Affiliations
- Hebei Normal University (CN)
- Corresponding author
- Bi, Caili
- Venue
- Plant Physiology and Biochemistry
- Publisher
- Elsevier BV
- Published
- 2024-07
- Volume
- 212
- Pages
- 108794
- ISSN
- 0981-9428 (ISSN-L)
- OpenAlex
- W4399284196
- Cited by
- 22
- References
- 44
- Citations by year
- 2026: 13 · 2025: 8 · 2024: 1
- FWCI
- 5.39
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Plant Physiology and Biochemistry (publishedVersion)
- SSRN Electronic Journal (acceptedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant Gene Expression Analysis
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- WRKY transcription factors, drought tolerance, secondary cell wall biosynthesis, lignin biosynthesis, cellulose biosynthesis, abscisic acid signaling, rice, transgenic overexpression, promoter binding, stress tolerance
- MeSH terms
- Abscisic Acid, Cell Wall, Cellulose, Lignin, Plant Proteins, Oryza, Stress, Physiological, Transcription Factors, Gene Expression Regulation, Plant, Plants, Genetically Modified, Droughts
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