Transcription factor-mediated gene regulatory networks contributes to reproductive stage drought tolerance in rice (Oryza sativa)


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Authors

  • SIMARDEEP KAUR ICAR-Indian Agricultural Research Institute, New Delhi 110 012, India image/svg+xml
  • KARISHMA SEEM College of Agriculture and Applied Sciences, Utah State University, Logan, Utah, USA image/svg+xml
  • TAMIL SELVAN S 3College of Agriculture and Applied Sciences, Utah State University, Logan, Utah, USA image/svg+xml
  • DWIJESH CHANDRA MISHRA College of Agriculture and Applied Sciences, Utah State University, Logan, Utah, USA image/svg+xml
  • RAKESH KAUNDAL College of Agriculture and Applied Sciences, Utah State University, Logan, Utah, USA
  • SURESH KUMAR College of Agriculture and Applied Sciences, Utah State University, Logan, Utah, USA image/svg+xml
  • TRILOCHAN MOHAPATRA Protection of Plant Varieties and Farmers' Rights Authority, New Delhi

https://doi.org/10.56093/ijas.v94i9.144862

Keywords:

Climate-resilient variety, Drought tolerance, Gene regulation, Rice, Terminal drought, Transcription factor

Abstract

Present study was carried out during rainy (kharif) seasons of 2020–22 at ICAR-Indian Agricultural Research Institute, New Delhi, to examine transcription factors (TFs) in drought tolerance using two rice (Oryza sativa L.) cultivars, drought-tolerant Nagina-22 and drought-sensitive IR-64. Immature panicles were used to prepare transcriptome libraries, sequenced with Paired-End 150 bp chemistry for both control and drought-treated samples. Bioinformatic analysis of the data using TFs extracted from PlantTF database revealed that majority (335) of the TFs were up-regulated in Nagina-22, while 92 were down-regulated under stress. Conversely, a significant number of TFs (359) were down-regulated in IR-64 under stress. Gene ontology and gene regulatory network analyses of the differentially expressed TFs indicated that several crucial biological processes and molecular functions were enriched with higher number of up-regulated TFs in Nagina-22 under stress. Significantly up-regulated expression of TFs, particularly WRKY, ERF, MYB, NAC, and bHLH, in panicle of N-22 must be responsible for terminal drought tolerance. Our findings confirm the master-regulator role of TFs in gene-regulatory networks essential for tolerance to complex trait like drought. The information might be valuable in selecting potential candidate parental lines for drought tolerance breeding and genetic manipulation of rice cultivars towards the development of climate-resilient cultivars.

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References

Dobin A, Davis C A, Schlesinger F, Drenkow J, Zaleski C, Jha S and Gingeras T R. 2013. STAR: Ultrafast universal RNA-seq aligner. Bioinformatics 29(1): 15–21. DOI: https://doi.org/10.1093/bioinformatics/bts635

Duhan N and Kaundal R. 2020. pySeqRNA: An automated Python package for RNA sequencing data analysis.

Guo J, Sun B, He H, Zhang Y, Tian H and Wang B. 2021. Current understanding of bHLH transcription factors in plant abiotic stress tolerance. International Journal of Molecular Sciences 22(9): 4921. DOI: https://doi.org/10.3390/ijms22094921

Huang K, Wu T, Ma Z, Li Z, Chen H, Zhang M and Du X. 2021. Rice transcription factor OsWRKY55 is involved in the drought response and regulation of plant growth. International Journal of Molecular Sciences 22(9): 4337. DOI: https://doi.org/10.3390/ijms22094337

Jin Y, Pan W, Zheng X, Cheng X, Liu M, Ma H and Ge X. 2018. OsERF101, an ERF family transcription factor, regulates drought stress response in reproductive tissues. Plant Molecular Biology 98: 51–65. DOI: https://doi.org/10.1007/s11103-018-0762-5

Jung S E, Kim T H, Shim J S, Bang S W, Yoon H B, Oh S H, Kim Y S, Oh S J, Seo J S and Kim J K. 2022. Rice NAC17 transcription factor enhances drought tolerance by modulating lignin accumulation. Plant Science 323: 111404. DOI: https://doi.org/10.1016/j.plantsci.2022.111404

Kaur S, Seem K, Duhan N, Kumar S, Kaundal R and Mohapatra T. 2023a. Transcriptome and physio-biochemical profiling reveals differential responses of rice cultivars at reproductive-stage drought stress. International Journal of Molecular Sciences 24(2): 1002. DOI: https://doi.org/10.3390/ijms24021002

Kaur S, Seem K, Kumar S, Kaundal R and Mohapatra T. 2023b. Comparative genome-wide analysis of microRNAs and their target genes in roots of contrasting indica rice cultivars under reproductive-stage drought. Genes 14(7): 1390. DOI: https://doi.org/10.3390/genes14071390

Kumar S, Seem K, Kumar S and Mohapatra T. 2022a. RNA-seq analysis reveals the genes/pathways responsible for genetic plasticity of rice to varying environmental conditions on direct-sowing and transplanting. Scientific Reports 12(1): 2241. DOI: https://doi.org/10.1038/s41598-022-06009-w

Kumar S, Kumar S, Krishnan S G and Mohapatra T. 2022b. Molecular basis of genetic plasticity to varying environmental conditions on growing rice by dry/direct-sowing and exposure to drought stress: Insights for DSR varietal development. Frontiers in Plant Science 13: 1013207. DOI: https://doi.org/10.3389/fpls.2022.1013207

Li J, Han G, Sun C and Sui N. 2019. Research advances of MYB transcription factors in plant stress resistance and breeding. Plant Signaling and Behavior 14(8): 1613131. DOI: https://doi.org/10.1080/15592324.2019.1613131

Li W, Pang S, Lu Z and Jin B. 2020. Function and mechanism of WRKY transcription factors in abiotic stress responses of plants. Plants 9(11): 1515. DOI: https://doi.org/10.3390/plants9111515

Liang Y, Tabien R E, Tarpley L, Mohammed A R and Septiningsih E M. 2021. Transcriptome profiling of two rice genotypes under mild field drought stress during grain-filling stage. AoB Plants 13(4): plab043. DOI: https://doi.org/10.1093/aobpla/plab043

Liao Y, Smyth G K and Shi W. 2014. FeatureCounts: An efficient general purpose programme for assigning sequence reads to genomic features. Bioinformatics 30(7): 923–30. DOI: https://doi.org/10.1093/bioinformatics/btt656

Love M I, Huber W and Anders S. 2014. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome biology 15(12): 1–21. DOI: https://doi.org/10.1186/s13059-014-0550-8

Qian Y, Zhang T, Yu Y, Gou L, Yang J, Xu J and Pi E. 2021. Regulatory mechanisms of bHLH transcription factors in plant adaptive responses to various abiotic stresses. Frontiers in Plant Science 12: 677611. DOI: https://doi.org/10.3389/fpls.2021.677611

Srinivasan R, Ramachandran G N, El-Manzalawy Y and Honavar V. 2013. Benjamini–Hochberg Method. Encyclopedia of Systems Biology 78–78. DOI: https://doi.org/10.1007/978-1-4419-9863-7_1215

Tolosa L N and Zhang Z. 2020. The role of major transcription factors in Solanaceous food crops under different stress conditions: Current and future perspectives. Plants 9(1): 56. DOI: https://doi.org/10.3390/plants9010056

Welner D H, Deeba F, Leggio L L and Skriver K. 2016. NAC transcription factors: From structure to function in stress- associated networks. Plant Transcription Factors, pp. 199–212. Daniel H Gonzalez (Ed). Academic Press. DOI: https://doi.org/10.1016/B978-0-12-800854-6.00013-0

Yao C, Li X, Li Y, Yang G, Liu W, Shao B and Han D. 2022. Overexpression of a Malus baccata MYB transcription factor gene MbMYB4 increases cold and drought tolerance in Arabidopsis thaliana. International Journal of Molecular Sciences 23(3): 1794. DOI: https://doi.org/10.3390/ijms23031794

Yao P F, Li C L, Zhao X R, Li M F, Zhao H X and Guo J Y. 2017. Overexpression of a tartary buckwheat gene, FtbHLH3, enhances drought/oxidative stress tolerance in transgenic Arabidopsis. Frontiers in Plant Science 8: 625. DOI: https://doi.org/10.3389/fpls.2017.00625

Yoon Y, Seo D H, Shin H, Kim H J, Kim C M and Jang G. 2020. The role of stress-responsive transcription factors in modulating abiotic stress tolerance in plants. Agronomy 10(6): 788. DOI: https://doi.org/10.3390/agronomy10060788

Submitted

2023-11-04

Published

2024-09-11

Issue

Section

Articles

How to Cite

KAUR, S. ., SEEM, K. ., S, T. S. ., MISHRA, D. C. ., KAUNDAL, R., KUMAR, S. ., & MOHAPATRA, T. . (2024). Transcription factor-mediated gene regulatory networks contributes to reproductive stage drought tolerance in rice (Oryza sativa). The Indian Journal of Agricultural Sciences, 94(9), 935–939. https://doi.org/10.56093/ijas.v94i9.144862
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