Multi-gene transformation evaluation of a serine/threonine protein kinase with a gene from the cytokinin oxidase/dehydrogenase family and a transcription factor induced under stress from the NAM-ATAF-CUC family to rice

Document Type : Original Research

Authors

1 Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research Education and Extension Organization (AREEO)

2 Rice Research Institute of Iran (RRII), Agricultural Research Education and Extension Organization (AREEO)

3 Assistant Professor, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research Education and Extension Organization (AREEO)

4 Professor, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research Education and Extension Organization (AREEO)

Abstract
Production of drought tolerant crop is an important strategy for avoiding water scarce crisis. Improvement of the root structure leading to the higher yield and seed quality. In this study, three genes affecting root structure, drought tolerance and phosphorous absorbance are used in producing hybrid constructs used for the rice transformation. Three genes: a serine/threonine protein kinase (PSTOL1), a gene from the cytokinin oxidase/dehydrogenase family (OsCKX4) and a transcription factor induced under stress from the NAM-ATAF-CUC family (OsNAC5) isolated from the rice wild cultivars are cloned under separate regulatory elements in the T-DNA region of the Agrobacterium binary vector. OsNAC5 gene was cloned under RCc3 root specific promoter and PSTOL1 gene under ubiquitin promoter. Also, OsCKX4 gene was cloned once under ubiquitin promoter and once under RCc3 promoter. Two hybrid multi-gene constructs named pUhrN5CkPstol and pUhrCkPstol harboring multiple genes are synthetized and used for the gene transformation into the Hashemi cultivar. Gene transfer was done to callus obtained from mature rice seeds. Transgenic plants were confirmed using PCR analysis. From the number of 107 regenerated plants in which the presence of transgenes was proved, 14 transgenic events were finally obtained. Root structure of the T0 plants showed drastic phenotypic difference in comparison to the non-transgenic ones. By now, one transgenic event harboring CKX4 and PSTOL1 is confirmed to have a homozygous line in T2 generation. It is hoped that genetic engineering of rice for enhanced root structure lead to drought tolerance, reduce water consumption and improve yield under stress conditions.

Keywords

Subjects


1. Zhang, Q. Strategies for developing green super rice. (2007) Proc. Natl. Acad. Sci. 104, 16402–16409
2. Gowda, V. R. P., Henry, A., Yamauchi, A., Shashidhar, H. E. & Serraj, R. (2011) Root biology and genetic improvement for drought avoidance in rice. F. Crop. Res. 122, 1–13
3. Tran, L.-S. P., Nishiyama, R., Yamaguchi-Shinozaki, K. & Shinozaki, K. (2010) Potential utilization of NAC transcription factors to enhance abiotic stress tolerance in plants by biotechnological approach. GM Crops 1, 32–39
4. Sperotto, R. A. et al. (2009) Identification of up-regulated genes in flag leaves during rice grain filling and characterization of OsNAC5, a new ABA-dependent transcription factor. Planta 230, 985–1002
5. Wu, W. & Cheng, S. (2014) Root genetic research, an opportunity and challenge to rice improvement. F. Crop. Res. 165, 111–124
6. Jeong, J. S. et al. (2013) OsNAC5 overexpression enlarges root diameter in rice plants leading to enhanced drought tolerance and increased grain yield in the field. 10, 101–114
7. Redillas, M. C. F. R. et al. (2012) The overexpression of OsNAC9 alters the root architecture of rice plants enhancing drought resistance and grain yield under field conditions. Plant Biotechnol. J. 10, 792–805
8. Takasaki, H. et al. (2010) The abiotic stress-responsive NAC-type transcription factor OsNAC5 regulates stress-inducible genes and stress tolerance in rice. Mol. Genet. Genomics 284, 173–183
9. Song, S.-Y., Chen, Y., Chen, J., Dai, X.-Y. & Zhang, W.-H. (2011) Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress. Planta 234, 331–345
10. Gao, S. et al. (2014) Cytokinin Oxidase/Dehydrogenase4 integrates cytokinin and auxin signaling to control rice crown root formation. Plant Physiol. 165, 1035–1046
11. Shahbazi, K. & Besharati, H. (2013) Overview of agricultural soil fertility status of Iran. L. Manag. J. 1, 1–15
12. Miyasaka, S. C. & Habte, M. (2007) Plant mechanisms and mycorrhizal symbioses to increase phosphorus uptake efficiency. Commun. Soil Sci. Plant Anal. 32, 1101–1147
13. Wissuwa, M., Wegner, J., Ae, N. & Yano, M. (2002) Substitution mapping of Pup1 : a major QTL increasing phosphorus uptake of rice from a phosphorus-deficient soil. 890–897
14. Wissuwa, M. (2005) Combining a modelling with a genetic approach in establishing associations between genetic and physiological effects in relation to phosphorus uptake. Plant Soil 269, 57–68
15. Heuer, S. et al. (2009) Comparative sequence analyses of the major quantitative trait locus phosphorus uptake 1 (Pup1) reveal a complex genetic structure. Plant Biotechnol. J. 7, 456–471
16. Gamuyao, R. et al. (2012) confers tolerance of phosphorus deficiency. Nature 488, 535–539
17. Chin, J. H. et al. (2011) Developing rice with high yield under phosphorus deficiency: Pup1 sequence to application. Plant Physiol. 156, 1202–1216
18. Chin, J. H. et al. (2010) Development and application of gene-based markers for the major rice QTL Phosphorus uptake 1. Theor. Appl. Genet. 120, 1073–1086
19. Sambrook, J., Fritsch, E. F. & Maniatis, T. (1989) Molecular cloning: a laboratory manual. (Cold spring harbor laboratory press)
20. An, G., Watson, B. D. & Chiang, C. C. (1986) Transformation of tobacco, tomato, potato, and Arabidopsis thaliana using a binary Ti vector system. Plant Physiol. 81, 301–305
21. Chamani, M. F. et al. (2017) Isolation and functional analysis of PSTOL1 from wild species of rice. Gene Eng Biosafety J 6 (1), 1-10
22. Kazemi, M. et al. (2022) Rice genetic engineering using transformation of Deeper Rooting1 and Phosphorus-Starvation Tolerance1 genes. Agric. Biotechnol. J. 14, 1–20
23. Zandi, M., Hosseini, R., Mohsenpour, M., Hosseini, S. G. & Ghareyazie, B. (2019) Transformation of DRO1, OsNAC5, OsEXPA8 genes in order to improve rice root architecture modification and improved drought tolerance in rice. Gene Eng Biosafety J 8 (1), 77-89
24. Ozawa, K. (2012) A high-efficiency Agrobacterium-mediated transformation system of rice (Oryza sativa L.). in Transgenic Plants 51–57
25. Chamani Mohasses, F., Solouki, M., Ghareyazie, B., Fahmideh, L. & Mohsenpour, M. (2020) Correlation between gene expression levels under drought stress and synonymous codon usage in rice plant by in-silico study. PLoS One 15, e0237334
26. Kahak, S. et al. (2021) Providing a Fast and Multiple Method for Detection and Identification of Transgenic Maize Events. MGJ 16, 341–348
27. Jeong, J. S. et al. (2013) OsNAC5 overexpression enlarges root diameter in rice plants leading to enhanced drought tolerance and increased grain yield in the field. Plant Biotechnol. J. 11, 101–114
28. Mohsenpour, M., Noormohammadi, Z., Irani, S. & Amirmozafari, N. (2019) Expression of an Environmentally Friendly Enzyme, Engineered Carbonic Anhydrase, in Escherichia coli. Int. J. Environ. Res. 13, 295–301
29. Kahak, S., Ghareyazie, B., Samizadeh Lahiji, H. & Mohsenpour, M. (2021) Evaluation of Biosafety Aspects of Cisgenesis and Intragenesis in Comparison with Transgenesis. gebsj 10, 157–170
30. Mohammadizadeh, N., Tohidfar, M. & Mohsenpour, M. (2010) Agrobacterium-Mediated Transformation of Wheat (Triticum Aestivum) Using Chitinase and Glucanase Genes. Agric Biotechnol J 2 (1), 81-98
31. Raufi, A., Tohidfar, M., Soluki, M. & Mohsenpour, M. (2012) Isolation and Cloning of Two Genes from PR1 Family and Construction of Treble Plasmids Containing 3 Groups of Genes for Producing Transformed Plants Resistant to Fungal Diseases. J. Agric. Biotechnol. 3, 27–46
32. Mohsenpour, M., Tohidfar, M., Jelodar, N. B. & Jouzani, G. S. (2015) Designing a new marker-free and tissue-specific platform for molecular farming applications. J. Plant Biochem. Biotechnol. 24, doi: 10.1007/s13562-014-0294-2
33. Mohkami, A., Marashi, H., Shahriary Ahmadi, F., Tohidfar, M. & Mohsenpour, M. (2015) Evaluation of Agrobacterium-mediated Transformation of Chlamydomonas reinhardtii using a Synthetic amorpha-4, 11-diene Synthase Gene. J. Cell Mol. Res. 7, 53–58
34. Mohsenpour, M. & Tohidfar, M. (2011) Genetic Engineering of Plant Nuclear Genome for Specific gene Expression in Chloroplast Using Design and Transformation of Hybrid Sigma Factor. Crop Biotechnol. 1, 35-48
35. Saboori-Robat, E., Solouki, M., Habashi, A. A., Moshenpour, M. & Emamjomeh, A. (2019) Design and construction of two-genes construct consists of 11 kDa delta zein and EPSPS genes in order to transform soybean to improve the methionine content and induce resistance to glyphosate herbicide. Crop Biotechnol. 9, 69–77
36. Ghareyazie, B. et al. (1997) Enhanced resistance to two stem borers in an aromatic rice containing a synthetic cryIA(b) gene. Mol. Breed. 3, 401–414
37. Bennett, J., Cohen, M. B., Katiyar, S. K., Ghareyazie, B. & Khush, G. S. (1997) Enhancing insect resistance in rice through biotechnology. Adv. insect Control role transgenic plants 75–93
38. Ghorbanzadeh, Z. et al. (2022) Identificatioan and investigation of DRO1 gene in rice cultivar Hashemi and its simultaneous transfer with OsCKX4 gene to improve root structure. Crop Biotechnol. 11, 49–62
39. Ye, X. et al. (2000) Engineering the provitamin A (β-carotene) biosynthetic pathway into (carotenoid-free) rice endosperm. Science (80-. ). 287, 303–305
40. Li, L. et al. (2003) Combinatorial modification of multiple lignin traits in trees through multigene cotransformation. Proc. Natl. Acad. Sci. 100, 4939–4944
41. Mohsenpour, M., Kahak, S. & Ghareyazie, B. (2018) Genetic Engineering and Food Security. Strateg. Res. J. Agric. Sci. Nat. Resour. 3, 195–208