Comparative analysis of cis-regulatory elements associated with salinity and drought tolerance in rice (oryza sativa l.) using in silico analysis

Bui Thi Hai Hoa, Nguyen Huy Duong, Dinh Thi Thu Le, Trinh Thi Thu Hang, Vu Kim Thoa, Le Thu Thuy, Bui Van Ngoc
Author affiliations

Authors

  • Bui Thi Hai Hoa \(^1\) Institute of Food and Biotechnology - Ha Noi Open University, 101B Nguyen Hien, Hai Ba Trung District, Ha Noi, Vietnam
  • Nguyen Huy Duong \(^2\) Institute of Biotechnology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Hanoi, Vietnam https://orcid.org/0000-0001-8313-3455
  • Dinh Thi Thu Le \(^1\) Institute of Food and Biotechnology - Ha Noi Open University, 101B Nguyen Hien, Hai Ba Trung District, Ha Noi, Vietnam https://orcid.org/0009-0003-4992-1986
  • Trinh Thi Thu Hang \(^1\) Institute of Food and Biotechnology - Ha Noi Open University, 101B Nguyen Hien, Hai Ba Trung District, Ha Noi, Vietnam
  • Vu Kim Thoa \(^1\) Institute of Food and Biotechnology - Ha Noi Open University, 101B Nguyen Hien, Hai Ba Trung District, Ha Noi, Vietnam https://orcid.org/0009-0006-0735-1366
  • Le Thu Thuy \(^2\) Institute of Biotechnology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Hanoi, Vietnam
  • Bui Van Ngoc \(^2\) Institute of Biotechnology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Hanoi, Vietnam
    \(^3\) Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Hanoi, Vietnam
    https://orcid.org/0000-0002-4659-7338

DOI:

https://doi.org/10.15625/vjbt-18581

Keywords:

Cis-regulatory elements (cREs), Ion transporters, Rice, Salinity tolerance, In silico analysis

Abstract

The critical roles of cis-regulatory elements (cREs) in the regulation of gene expression in response to environmental stress were reported in previous studies. Although transcription factor families to regulate gene expression in plants are well documented, there is a limited number of cREs related to salinity and drought tolerance in rice to be identified. Therefore, in this study, a comparative analysis and characterization of cREs associated with specific drought and salinity tolerance genes of rice, namely OsNHX1, OsNHX5, OsHKT1;1, OsHKT2;1, and OsSOS1, was performed using the PLACE and PlantPAN 3.0 databases, along with in silico methods. Several cis-elements within the core promoter region, including TATA-box, CAAT-box, G-box, DPE, and Y-Patch were identified. Additionally, eight other cis elements: ABRE, MYBRS, MYCRS, NAC-binding site, ACGTATERD1, GT1GMSCAM4, W-box, and DRE, were discovered and suggested to be potentially involved in drought and salinity tolerance in rice.  Comparative analysis revealed that OsNHX1 and OsHKT1;1 exhibit a higher abundance of cREs compared to the other genes studied. The presence of an increased number of cREs suggests a more complex regulatory network, potentially enhancing the ability of these genes to cope with environmental stressors and fine-tune their responses to changing conditions. Furthermore, understanding the distribution and diversity of cREs across different genes can offer practical implications for genetic engineering and crop improvement strategies. Genes with desirable regulatory profiles, especially those associated with specific stress tolerances, may be prime candidates for genetic manipulation.

Downloads

Download data is not yet available.

References

Apse MP, Blumwald, E (2007) Na+ transport in plants. FEBS Letters 581: 2247-2254. https://doi.org/10.1016/j.febslet.2007.04.014

Basu S, Roychoudhury A (2014) Expression profiling of abiotic stress-inducible genes in response to multiple stresses in rice (Oryza sativa L.) varieties with contrasting level of stress tolerance. Biomed Res Int 2014: 706890. https://doi.org/10.1155/2014/706890

Civan P, Svec M (2009) Genome-wide analysis of rice (Oryza sativa L. subsp. japonica) TATA box and Y Patch promoter elements. Genome 52: 294-297. https://doi.org/10.1139/g09-001

Cui MH, Yoo KS, Hyoung S, Nguyen HT, Kim YY, Kim HJ, Shin JS (2013) An Arabidopsis R2R3-MYB transcription factor, AtMYB20, negatively regulates type 2C serine/threonine protein phosphatases to enhance salt tolerance. FEBS Lett 587: 1773-1778. https://doi.org/10.1016/j.febslet.2013.04.028

de Medeiros Oliveira M, Bonadio I, Lie de Melo A, Mendes Souza G, Durham AM (2021) TSSFinder-fast and accurate ab initio prediction of the core promoter in eukaryotic genomes. Brief bioinfor 22: bbab198. https://doi.org/10.1093/bib/bbab198

Farooq M, Park JR, Jang YH, Kim EG, Kim KM (2021) Rice Cultivars Under Salt Stress Show Differential Expression of Genes Related to the Regulation of Na+/K+ Balance. Front Plant Sci 12: 680131. https://doi.org/10.3389/fpls.2021.680131

Feng RJ, Ren MY, Lu LF, Peng M, Guan X, Zhou DB, Zhang MY, Qi DF, Li K, Tang W, Yun TY, Chen YF, Wang F, Zhang D, Shen Q, Liang P, Zhang YD, Xie JH (2019) Involvement of abscisic acid-responsive element-binding factors in cassava (Manihot esculenta) dehydration stress response. Sci Rep 9(1): 12661 https://doi.org/10.1038/s41598-019-49083-3

Freitas EO, Melo BP, Lourenço-Tessutti IT, Arraes FBM, Amorim RM, Lisei-de-Sá ME, Costa JA, Leite AGB, Faheem M, Ferreira MA, Morgante CV, Fontes EPB, Grossi-de-Sa MF (2019) Identification and characterization of the GmRD26 soybean promoter in response to abiotic stresses: potential tool for biotechnological application. BMC Biotechnol 19(1): 79. https://doi.org/10.1186/s12896-019-0561-3

Fukuda A, Nakamura A, Hara N, Toki S, Tanaka Y (2011) Molecular and functional analyses of rice NHX-type Na+/H+ antiporter genes. Planta 233: 175-188. https://doi.org/10.1007/s00425-010-1289-4

Garciadeblas B, Senn ME, Banuelos MA, Rodriguez-Navarro A (2003) Sodium transport and HKT transporters: the rice model. Plant J 34: 788-801. https://doi.org/10.1046/j.1365-313x.2003.01764.x

Hauser F, Horie T (2010) A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K(+)/Na(+) ratio in leaves during salinity stress. Plant Cell Environ 33: 552-565. https://doi.org/10.1111/j.1365-3040.2009.02056.x

Jiang Y, Deyholos MK (2009) Functional characterization of Arabidopsis NaCl-inducible WRKY25 and WRKY33 transcription factors in abiotic stresses. Plant Mol Biol 69: 91-105. https://doi.org/10.1007/s11103-008-9408-3

Jiang Y, Yang B, Deyholos MK (2009) Functional characterization of the Arabidopsis bHLH92 transcription factor in abiotic stress. Mol Genet Genomics 282: 503-516. https://doi.org/10.1007/s00438-009-0481-3

Joshi R, Wani SH, Singh B, Bohra A, Dar ZA, Lone AA, Pareek A, Singla-Pareek SL (2016) Transcription Factors and Plants Response to Drought Stress: Current Understanding and Future Directions. Front Plant Sci 7: 1029. https://doi.org/10.3389/fpls.2016.01029

Kasuga M, Liu Q, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1999) Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor. Nat Biotechnol 17: 287-291. https://doi.org/10.1038/7036

Kobayashi Y, Murata M, Minami H, Yamamoto S, Kagaya Y, Hobo T, Yamamoto A, Hattori T (2005) Abscisic acid-activated SNRK2 protein kinases function in the gene-regulation pathway of ABA signal transduction by phosphorylating ABA response element-binding factors. Plant J 44(6), 939–949. https://doi.org/10.1111/j.1365-313x.2005.02583.x

Kuwano M, Masumura T, Yoshida KT (2011) A novel endosperm transfer cell-containing region-specific gene and its promoter in rice. Plant Mol Biol 76: 47-56. https://doi.org/10.1007/s11103-011-9765-1

Liang L, Guo L, Zhai Y, Hou Z, Wu W, Zhang X, Wu Y, Liu X, Guo S, Gao G, Liu W (2023) Genome-wide characterization of SOS1 gene family in potato (Solanum tuberosum) and expression analyses under salt and hormone stress. Front Plant Sci, 14: 1201730. https://doi.org/10.3389/fpls.2023.1201730

Liang M H, Jiang JG (2017) Analysis of carotenogenic genes promoters and WRKY transcription factors in response to salt stress in Dunaliella bardawil. Sci Rep 7: 37025. https://doi.org/10.1038/srep37025

Liu C, Mao B, Yuan D, Chu C, Duan M (2022) Salt tolerance in rice: Physiological responses and molecular mechanisms. The Crop Journal 10: 13-25. https://doi.org/10.1016/j.cj.2021.02.010

Martínez-Atienza J, Jiang X, Garciadeblas B, Mendoza I, Zhu JK, Pardo JM, Quintero FJ (2007) Conservation of the salt overly sensitive pathway in rice. Plant Physiol 143: 1001–1012. https://doi.org/10.1104/pp.106.092635

Miyoshi SI, Sasaki T, Kaku N, Inoue T, Uozumi N, Maehara Y, Nakao H (2010) Assimilation of Metal Ions Bound to Porphyrins or Porphyrin-Peptides by Vibrio vulnificus, a Human Pathogen Inhabiting Estuarine and Marine Environments. Biocontrol Science 15: 1-6. https://doi.org/10.4265/bio.15.1

Nardone V, Chaves-Sanjuan A, Nardini M (2017) Structural determinants for NF-Y/DNA interaction at the CCAAT box. Biochim Biophys Acta Gene Regul Mech 1860(5): 571–580. https://doi.org/10.1016/j.bbagrm.2016.09.006

Reese MG (2001) Application of a time-delay neural network to promoter annotation in the Drosophila melanogaster genome. Comput Chem 26: 51-56. https://doi.org/10.1016/s0097-8485(01)00099-7

Shaban AS, Safhi FA, Fakhr M A, Pruthi R, Abozahra MS, El-Tahan AM, Subudhi PK (2023) Comparison of the Morpho-Physiological and Molecular Responses to Salinity and Alkalinity Stresses in Rice. Plants (Basel, Switzerland) 13(1): 60. https://doi.org/10.3390/plants13010060

Shahmuradov IA, Umarov RK, Solovyev VV (2017) TSSPlant: a new tool for prediction of plant Pol II promoters. Nucleic Acids Res 45: e65.https://doi.org/10.1093%2Fnar%2Fgkw1353

Shi H, Ishitani M, Kim C, Zhu JK (2000) The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter. Proc Natl Acad Sci 97: 6896–6901. https://doi.org/10.1073/pnas.120170197

Shi H, Quintero FJ, Pardo JM, Zhu JK (2002) The putative plasma membrane Na(+)/H (+) antiporter SOS1 controls long-distance Na(+) transport in plants. Plant Cell 14: 465-477. https://doi.org/10.1105/tpc.010371

Tran LS, Nakashima K, Sakuma Y, Simpson SD, Fujita Y, Maruyama K, Yamaguchi-Shinozaki K (2004) Isolation and functional analysis of Arabidopsis stress-inducible NAC transcription factors that bind to a drought-responsive cis-element in the early responsive to dehydration stress 1 promoter. Plant Cell 16: 2481-2498. https://doi.org/10.1105/tpc.104.022699

Van Nguyen N, Ferrero A (2006) Meeting the challenges of global rice production. Paddy Water Environ 4: 1-9. https://doi.org/10.1007/s10333-005-0031-5

Wang X, Bandyopadhyay S, Xuan Z, Zhao X, Zhang MQ, Zhang X (2007) Prediction of transcription start sites based on feature selection using AMOSA. Proc LSS Comput Syst Bioinform Conf 6: 183–193.

Yamaguchi T, Hamamoto S, Uozumi N (2013) Sodium transport system in plant cells Front Plant Sci 4: 410. https://doi.org/10.3389/fpls.2013.00410

Yamamoto YY, Ichida H, Matsui M, Obokata J, Sakurai T, Satou M, Abe T (2007) Identification of plant promoter constituents by analysis of local distribution of short sequences. BMC Genomics 8: 67. https://doi.org/10.1186/1471-2164-8-67

Yang O, Popova OV, Suthoff U, Luking I, Dietz KJ, Golldack D (2009) The Arabidopsis basic leucine zipper transcription factor AtbZIP24 regulates complex transcriptional networks involved in abiotic stress resistance. Gene 436: 45-55. https://doi.org/10.1016/j.gene.2009.02.010

Yu, Y., Qian, Y., Jiang, M., Xu, J., Yang, J., Zhang, T., Gou, L., & Pi, E. (2020). Regulation Mechanisms of Plant Basic Leucine Zippers to Various Abiotic Stresses. Front Plant Sci 11: 1258. https://doi.org/10.3389%2Ffpls.2020.01258

Zhu J, Ren Y, Wang Y, Liu F, Teng X, Zhang Y, Duan E, Wu M, Zhong M, Hao Y, Zhu X, Lei J, Wang Y, Yu Y, Pan T, Bao Y, Wang Y, Wan J (2019) OsNHX5-mediated pH homeostasis is required for post-Golgi trafficking of seed storage proteins in rice endosperm cells. BMC plant biol, 19(1): 295. https://doi.org/10.1186/s12870-019-1911-y

Downloads

Published

30-06-2024

How to Cite

Hoa, B. T. H., Duong, N. H., Le, D. T. T., Hang, T. T. T., Thoa, V. K., Thuy, L. T., & Ngoc, B. V. (2024). Comparative analysis of <i>cis</i>-regulatory elements associated with salinity and drought tolerance in rice (<i>oryza sativa l.</i>) using <i>in silico</i> analysis. Vietnam Journal of Biotechnology, 22(2), 289–304. https://doi.org/10.15625/vjbt-18581

Issue

Section

Articles