Target genes utilized for drought tolerance enhancement in maize
DOI:
https://doi.org/10.14719/pst.2561Keywords:
Drought stress, maize, overexpression, transgeneAbstract
Among the most widely grown cereal crops is maize, which is a staple food for millions of people worldwide. It is primarily used for human consumption in various forms, animal feed, and industrial applications. In many countries like Mexico, Africa, and South America, it is the main source of calories in their daily diet, making it crucial for food security. Many nations worldwide are more at risk of drought as global warming continues to accelerate. One of the major hurdles to food production in the twenty-first century and a serious threat to our present and future food security is a water crisis. Crop failure due to water scarcity can put millions of lives at risk. Along with traditional breeding, transgenic approaches are an essential tool in modern plant breeding. They allow the introduction of beneficial genes from other organisms or within the same organism to improve plant characteristics. This review focuses on specific genes that are stably expressed and tested for drought tolerance in maize. Several genes have been identified as potential targets for improving drought tolerance in maize. Although mechanisms of target genes overlap to some extent, we attempted to divide the selected research articles according to the mechanism of the targeted gene into categories and reviewed them.
Downloads
References
FAO. 2018. The impact of disasters and crises on agriculture and food security: 2017. Rome. http://www.fao.org/3/I8656EN/i8656en.pdf
Chaves MM. Mechanisms underlying plant resilience to water deficits: Prospects for water-saving agriculture. Journal of Experimental Botany. 2004;55(407):2365–84. https://doi.org/10.1093/jxb/erh269
Farooq M, Wahid A, Kobayashi N, Fujita D, Basra SM. Plant drought stress: Effects, mechanisms and management. Agronomy for Sustainable Development. 2009;29(1):185–212. https://doi.org/10.1051/agro:2008021
Sah RP, Chakraborty M, Prasad K, Pandit M, Tudu VK, Chakravarty MK, et al. Impact of water deficit stress in maize: Phenology and yield components. Scientific Reports. 2020;10(1). https://doi.org/10.1038/s41598-020-59689-7.
Iqbal S, Wang X, Mubeen I, Kamran M, Kanwal I, Díaz GA, et al. Phytohormones trigger drought tolerance in crop plants: Outlook and future perspectives. Frontiers in Plant Science. 2022; 12. doi:10.3389/fpls.2021.799318
Daszkowska-Golec A, Hossain MA, Wani SH, Bhattacharjee S, Burritt DJ, Tran LS. Drought Stress Tolerance in Plants, Vol 2 Volume 2. Springer; Berlin/Heidelberg, Germany: 2016. pp. 123–151.
Wahab, A., Abdi, G., Saleem, M. H., Ali, B., Ullah, S., Shah, W., Mumtaz, S., Yasin, G., Muresan, C. C., & Marc, R. A. (). Plants physio-biochemical and Phyto-hormonal responses to alleviate the adverse effects of Drought stress: A comprehensive review. Plants. 2022; 11(13), 1620. https://doi.org/10.3390/plants11131620
Liu X, Zhai S, Zhao Y, Sun B, Liu C, Yang A, et al. Overexpression of the phosphatidylinositol synthase gene (ZmPIS) conferring drought stress tolerance by altering membrane lipid composition and increasing ABA synthesis in maize. Plant Cell Environ. 2013;36(5):1037-55. https://doi.org/10.1111/pce.12040
Xiang Y, Sun X, Gao S, Qin F, Dai M. Deletion of an Endoplasmic Reticulum Stress Response Element in a ZmPP2C-A Gene Facilitates Drought Tolerance of Maize Seedlings. Mol Plant. 2017;10(3):456-469. https://doi.org/10.1016/j.molp.2016.10.003
Cao L, Lu X, Wang G, Zhang Q, Zhang X, Fan Z, et al. Maize ZmbZIP33 Is Involved in Drought Resistance and Recovery Ability Through an Abscisic acid-dependent Signaling Pathway. Front Plant Sci. 2021;12:629903. https://doi.org/10.3389/fpls.2021.629903
Arraes FB, Beneventi MA, Lisei de Sa ME, Paixao JF, Albuquerque EV, Marin SR, et al. Implications of ethylene biosynthesis and signaling in soybean drought stress tolerance. BMC Plant Biology. 2015;15(1). https://doi.org/10.1186%2Fs12870-015-0597-z
Shi J, Habben JE, Archibald RL, Drummond BJ, Chamberlin MA, Williams RW, et al. Overexpression of ARGOS Genes Modifies Plant Sensitivity to Ethylene, Leading to Improved Drought Tolerance in Both Arabidopsis and Maize. Plant Physiol. 2015;169(1):266-82. https://doi.org/10.1104/pp.15.00780
Zhu Y, Liu Y, Zhou K, Tian C, Aslam M, Zhang B, et al. Overexpression of ZmEREBP60 enhances drought tolerance in maize. J Plant Physiol. 2022;275:153763. https://doi.org/10.1016/j.jplph.2022.153763
Osakabe Y, Osakabe K, Shinozaki K, Tran LSP.. Response of plants to water stress. Frontiers in Plant Science 2014; 5. https://doi.org/10.3389/fpls.2014.00086
Shou H, Bordallo P, Wang K. Expression of the Nicotiana protein kinase (NPK1) enhanced drought tolerance in transgenic maize. J Exp Bot. 2004;55(399):1013-19. https://doi.org/10.1093/jxb/erh129
Wang X, Wang H, Liu S, Ferjani A, Li J, Yan J, et al. Genetic variation in ZmVPP1 contributes to drought tolerance in maize seedlings. Nat Genet. 2016;48(10):1233-41. https://doi.org/10.1038/ng.3636
Mao H, Wang H, Liu S, Li Z, Yang X, Yan J, et al. A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. Nature Communications. 2015;6(1). https://doi.org/10.1038/ncomms9326
Liu S, Liu X, Zhang X, Chang S, Ma C, Qin F. Co-Expression of ZmVPP1 with ZmNAC111 Confers Robust Drought Resistance in Maize. Genes (Basel). 2022;14(1):8. https://doi.org/10.3390/genes14010008
Kavi Kishor PB, Ganie SA, Wani SH, Guddimalli R, Karumanchi AR, Edupuganti S, et al. Nuclear factor (NF-y): Developmental and stress-responsive roles in the plant lineage. Journal of Plant Growth Regulation. 2022; 42(5), 2711–2735. https://doi.org/10.1007/s00344-022-10739-6
Wang B, Li Z, Ran Q, Li P, Peng Z, Zhang J. ZmNF-YB16 Overexpression Improves Drought Resistance and Yield by Enhancing Photosynthesis and the Antioxidant Capacity of Maize Plants. Front Plant Sci. 2018;9:709. https://doi.org/10.3389/fpls.2018.00709
Nuccio ML, Wu J, Mowers R, Zhou HP, Meghji M, Primavesi LF, et al. Expression of trehalose-6-phosphate phosphatase in maize ears improves yield in well-watered and drought conditions. Nature Biotechnology, 2015; 33(8), 862–869. https://doi.org/10.1038/nbt.3277
Oszvald M, Primavesi LF, Griffiths CA, Cohn J, Basu SS, Nuccio ML et al. Trehalose 6-Phosphate Regulates Photosynthesis and Assimilate Partitioning in Reproductive Tissue. Plant Physiol. 2018;176(4):2623-2638. https://doi.org/10.1104/pp.17.01673
Hatfield JL, Dold C. Water-use efficiency: Advances and challenges in a changing climate. Frontiers in Plant Science. 2019;10. https://doi.org/10.3389%2Ffpls.2019.00103
Jeanneau M, Gerentes D, Foueillassar X, Zivy M, Vidal J, Toppan A, et al. Improvement of drought tolerance in maize: towards the functional validation of the Zm-Asr1 gene and increase of water use efficiency by over-expressing C4-PEPC. Biochimie. 2002;84(11):1127-35. https://doi.org/10.1016/s0300-9084(02)00024-x
Wang CR, Yang AF, Yue GD, Gao Q, Yin HY, Zhang JR. Enhanced expression of phospholipase C 1 (ZmPLC1) improves drought tolerance in transgenic maize. Planta. 2008;227(5):1127-40. https://doi.org/10.1007/s00425-007-0686-9
Mao H, Wang H, Liu S, Li Z, Yang X, Yan J, et al. A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. Nat Commun. 2015;6:8326. https://doi.org/10.1038/ncomms9326
Li H, Han X, Liu X, Zhou M, Ren W, Zhao B, et al.. A leucine-rich repeat-receptor-like kinase gene SbER2-1 from sorghum (Sorghum bicolor L.) confers drought tolerance in maize. BMC Genomics. 2019 Oct 15;20(1):737. https://doi.org/10.1186/s12864-019-6143-x
Xu J, You X, Leng Y, Li Y, Lu Z, Huang Y, et al. Identification and alternative splicing profile of the raffinose synthase gene in grass species. International Journal of Molecular Sciences. 2023; 24(13), 11120. https://doi.org/10.3390/ijms241311120
Liu Y, Li T, Zhang C, Zhang W, Deng N, Dirk LMA, et al. Raffinose positively regulates maize drought tolerance by reducing leaf transpiration. Plant J. 2023 Jan 26. https://doi.org/10.1111/tpj.16116
Pirasteh?Anosheh H, Saed?Moucheshi A, Pakniyat H, Pessarakli M. Stomatal responses to drought stress. Water Stress and Crop Plants. 2016; 24–40. doi:10.1002/9781119054450.ch3
Xiong L, Ishitani M, Lee H, Zhu JK. The arabidopsis Los5/ABA3 locus encodes a molybdenum cofactor sulfurase and modulates cold stress– and osmotic stress–responsive gene expression. The Plant Cell. 2001; 13(9), 2063–2083. doi:10.1105/tpc.010101
Lu Y, Li Y, Zhang J, Xiao Y, Yue Y, Duan L, et al.. Overexpression of Arabidopsis molybdenum cofactor sulfurase gene confers drought tolerance in maize (Zea mays L.). PLoS One. 2013;8(1):e52126. https://doi.org/10.1371/journal.pone.0052126
Guo Y, Shi Y, Wang Y, Liu F, Li Z, Qi J, et al. The clade F PP2C phosphatase ZmPP84 negatively regulates drought tolerance by repressing stomatal closure in maize. New Phytol. 2023 Mar;237(5):1728-1744. https://doi.org/10.1111/nph.18647
Wasaya A, Zhang X, Fang Q, Yan Z. Root phenotyping for drought tolerance: A Review. Agronomy. 2018;8(11):241. https://doi.org/10.3390/agronomy8110241
Li Z, Zhang X, Zhao Y, Li Y, Zhang G, Peng Z, Zhang J. Enhancing auxin accumulation in maize root tips improves root growth and dwarfs plant height. Plant Biotechnol J. 2018 Jan;16(1):86-99. https://doi.org/10.1111/pbi.12751
Li Z, Liu C, Zhang Y, Wang B, Ran Q, Zhang J. The bHLH family member ZmPTF1 regulates drought tolerance in maize by promoting root development and abscisic acid synthesis. J Exp Bot. 2019 Oct 15;70(19):5471-5486. https://doi.org/10.1093/jxb/erz307
Zhang X, Mi Y, Mao H, Liu S, Chen L, Qin F. Genetic variation in ZmTIP1 contributes to root hair elongation and drought tolerance in maize. Plant Biotechnol J. 2020 May;18(5):1271-1283. https://doi.org/10.1111/pbi.13290
Downloads
Published
Versions
- 23-10-2023 (2)
- 20-10-2023 (1)
How to Cite
Issue
Section
License
Copyright (c) 2022 Mirzakhmedov Mukhammadjon, K Kamalova Lola, S Ayubov Mirzakamol, T Normurodova Kunduz, A Ubaydullaeva Khurshida, T Buriev Zabardast, Y Abdurakhmonov Ibrokhim
This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright and Licence details of published articles
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
Open Access Policy
Plant Science Today is an open access journal. There is no registration required to read any article. All published articles are distributed under the terms of the Creative Commons Attribution License (CC Attribution 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited (https://creativecommons.org/licenses/by/4.0/). Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).