Research Paper

A β-ketoacyl-CoA Synthase OsCUT1 Confers Increased Drought Tolerance in Rice

Expand
  • 1State Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
    2Jiangsu Provincial Engineering Research Center of Seed Industry Science and Technology, Nanjing 210095, China
    3Suzhou Chien-Shiung Institute of Technology, Taicang 215411, China
First author contact:

#These authors contributed equally to this work

Huang Ji (huangji@njau.edu.cn);
Zhang Hongsheng (hszhang@njau.edu.cn)

Received date: 2021-08-24

  Accepted date: 2021-12-13

  Online published: 2021-12-15

Abstract

Drought stress is one of the major environmental factors affecting crop growth and productivity. Cuticular wax plays essential roles in protecting plants from environmental stress via forming a hydrophobic barrier on leaf epidermis. In this study, we analyzed nine members (OsCUT1?OsCUT9) of β-ketoacyl-CoA synthase, the rate-limiting key enzyme for cuticular wax synthesis in rice by homology search and domain prediction. The expression levels of OsCUT genes under different abiotic stresses were investigated and OsCUT1 down-regulated by abiotic stress was selected for further function validation. Compared to the wild type, overexpression of OsCUT1 (OX-OsCUT1) exhibited significantly increased drought resistance. Epicuticular wax was increased on the leaf surface of OX-OsCUT1 and the chlorophyll leaching experiment showed that the cuticular permeability was decreased in the OX-OsCUT1 plants. Moreover, overexpression of OsCUT1 didn’t result in the significant changes of major agronomic traits. In total, these results suggested that OsCUT1 is a promising gene for engineering rice plants with enhanced drought tolerance.

Cite this article

Gao Xiuying, Zhang Ye, Zhang Hongsheng, Huang Ji . A β-ketoacyl-CoA Synthase OsCUT1 Confers Increased Drought Tolerance in Rice[J]. Rice Science, 2022 , 29(4) : 353 -362 . DOI: 10.1016/j.rsci.2021.12.009

References

[1] Buschhaus C, Jetter R. 2012. Composition and physiological function of the wax layers coating Arabidopsis leaves: β-amyrin negatively affects the intracuticular water barrier. Plant Physiol, 160(2): 1120-1129.
[2] Fiebig A, Mayfield J A, Miley N L, Chau S, Fischer R L, Preuss D. 2000. Alterations in CER6, a gene identical to CUT1, differentially affect long-chain lipid content on the surface of pollen and stems. Plant Cell, 12(10): 2001-2008.
[3] Franke R, Höfer R, Briesen I, Emsermann M, Efremova N, Yephremov A, Schreiber L. 2009. The DAISY gene from Arabidopsis encodes a fatty acid elongase condensing enzyme involved in the biosynthesis of aliphatic suberin in roots and the chalaza- micropyle region of seeds. Plant J, 57(1): 80-95.
[4] Gan L, Wang X L, Cheng Z J, Liu L L, Wang J L, Zhang Z, Ren Y L, Lei C L, Zhao Z C, Zhu S S, Lin Q B, Wu F Q, Guo X P, Wang J, Zhang X, Wan J M. 2016. Wax crystal-sparse leaf 3encoding a β-ketoacyl-CoA reductase is involved in cuticular wax biosynthesis in rice. Plant Cell Rep, 35(8): 1687-1698.
[5] Gan L, Zhu S S, Zhao Z C, Liu L L, Wang X L, Zhang Z, Zhang X, Wang J, Wang J L, Guo X P, Wan J M. 2017. Wax Crystal- Sparse Leaf 4, encoding a β-ketoacyl-coenzyme A synthase 6, is involved in rice cuticular wax accumulation. Plant Cell Rep, 36(10): 1655-1666.
[6] Gray J E, Holroyd G H, van der Lee F M, Bahrami A R, Sijmons P C, Woodward F I, Schuch W, Hetherington A M. 2000. The HIC signalling pathway links CO2 perception to stomatal development. Nature, 408: 713-716.
[7] Haslam T M, Kunst L. 2013. Extending the story of very-long- chain fatty acid elongation. Plant Sci, 210: 93-107.
[8] Hooker T S, Millar A A, Kunst L. 2002. Significance of the expression of the CER6 condensing enzyme for cuticular wax production in Arabidopsis. Plant Physiol, 129(4): 1568-1580.
[9] Islam M A, Du H, Ning J, He H Y, Xiong L Z. 2009. Characterization of Glossy1-homologous genes in rice involved in leaf wax accumulation and drought resistance. Plant Mol Biol, 70(4): 443-456.
[10] James D W Jr, Lim E, Keller J, Plooy I, Ralston E, Dooner H K. 1995. Directed tagging of the Arabidopsis FATTY ACID ELONGATION1 (FAE1) gene with the maize transposon activator. Plant Cell, 7(3): 309-319.
[11] Joubès J, Raffaele S, Bourdenx B, Garcia C, Laroche-Traineau J, Moreau P, Domergue F, Lessire R. 2008. The VLCFA elongase gene family in Arabidopsis thaliana: Phylogenetic analysis, 3D modelling and expression profiling. Plant Mol Biol, 67(5): 547-566.
[12] Kunst L, Samuels L. 2009. Plant cuticles shine: Advances in wax biosynthesis and export. Curr Opin Plant Biol, 12(6): 721-727.
[13] Lee S B, Suh M C. 2013. Recent advances in cuticular wax biosynthesis and its regulation in Arabidopsis. Mol Plant, 6(2): 246-249.
[14] Lee S B, Jung S J, Go Y S, Kim H U, Kim J K, Cho H J, Park O K, Suh M C. 2009. Two Arabidopsis 3-ketoacyl CoA synthase genes, KCS20and KCS2/DAISY, are functionally redundant in cuticular wax and root suberin biosynthesis, but differentially controlled by osmotic stress. Plant J, 60(3): 462-475.
[15] Lolle S J, Berlyn G P, Engstrom E M, Krolikowski K A, Reiter W D, Pruitt R E. 1997. Developmental regulation of cell interactions in the Arabidopsis fiddlehead-1 mutant: A role for the epidermal cell wall and cuticle. Dev Biol, 189(2): 311-321.
[16] Mao B G, Cheng Z J, Lei C L, Xu F H, Gao S W, Ren Y L, Wang J L, Zhang X, Wang J, Wu F Q, Guo X P, Liu X L, Wu C Y, Wang H Y, Wan J M. 2012. Wax crystal-sparse leaf2, a rice homologue of WAX2/GL1, is involved in synthesis of leaf cuticular wax. Planta, 235(1): 39-52.
[17] Millar A A, Clemens S, Zachgo S, Giblin E M, Taylor D C, Kunst L. 1999. CUT1, an Arabidopsis gene required for cuticular wax biosynthesis and pollen fertility, encodes a very-long-chain fatty acid condensing enzyme. Plant Cell, 11(5): 825-838.
[18] Pruitt R E, Vielle-Calzada J P, Ploense S E, Grossniklaus U, Lolle S J. 2000. FIDDLEHEAD, a gene required to suppress epidermal cell interactions in Arabidopsis, encodes a putative lipid biosynthetic enzyme. Proc Natl Acad Sci USA, 97(3): 1311-1316.
[19] Qi C H, Zhao X Y, Jiang H, Zheng P F, Liu H T, Li Y Y, Hao Y J. 2018. Isolation and functional identification of an apple MdCER1 gene. Plant Cell Tissue Organ Cult, 136(1): 1-13.
[20] Qin B X, Tang D, Huang J, Li M, Wu X R, Lu L L, Wang K J, Yu H X, Chen J M, Gu M H, Cheng Z K. 2011. Rice OsGL1-1 is involved in leaf cuticular wax and cuticle membrane. Mol Plant, 4(6): 985-995.
[21] Qin Y M, Pujol F M, Hu C Y, Feng J X, Kastaniotis A J, Hiltunen J K, Zhu Y X. 2007. Genetic and biochemical studies in yeast reveal that the cotton fibre-specific GhCER6 gene functions in fatty acid elongation. J Exp Bot, 58(3): 473-481.
[22] Samuels L, Kunst L, Jetter R. 2008. Sealing plant surfaces: Cuticular wax formation by epidermal cells. Annu Rev Plant Biol, 59: 683-707.
[23] Shepherd T, Wynne Griffiths D. 2006. The effects of stress on plant cuticular waxes. New Phytol, 171(3): 469-499.
[24] Suh M C, Samuels A L, Jetter R, Kunst L, Pollard M, Ohlrogge J, Beisson F. 2005. Cuticular lipid composition, surface structure, and gene expression in Arabidopsis stem epidermis. Plant Physiol, 139(4): 1649-1665.
[25] Wang X C, Guan Y Y, Zhang D, Dong X B, Tian L H, Qu L Q. 2017. A β-ketoacyl-CoA synthase is involved in rice leaf cuticular wax synthesis and requires a CER2-LIKE protein as a cofactor. Plant Physiol, 173(2): 944-955.
[26] Wei H B, Chen C, Ma X S, Zhang Y, Han J, Mei H W, Yu S W. 2017. Comparative analysis of expression profiles of panicle development among tolerant and sensitive rice in response to drought stress. Front Plant Sci, 8: 437.
[27] Ye W J, Hu S K, Wu L W, Ge C W, Cui Y T, Chen P, Wang X W, Xu J, Ren D Y, Dong G J, Qian Q, Guo L B. 2016. White stripe leaf 12 (WSL12), encoding a nucleoside diphosphate kinase 2 (OsNDPK2), regulates chloroplast development and abiotic stress response in rice (Oryza sativa L.). Mol Breed, 36: 57.
[28] Yeats T H, Rose J K C. 2013. The formation and function of plant cuticles. Plant Physiol, 163(1): 5-20.
[29] Yephremov A, Wisman E, Huijser P, Huijser C, Wellesen K, Saedler H. 1999. Characterization of the FIDDLEHEAD gene of Arabidopsis reveals a link between adhesion response and cell differentiation in the epidermis. Plant Cell, 11(11): 2187-2201.
[30] Yu D M, Ranathunge K, Huang H S, Pei Z Y, Franke R, Schreiber L, He C Z. 2008. Wax Crystal-Sparse Leaf1 encodes a β-ketoacyl CoA synthase involved in biosynthesis of cuticular waxes on rice leaf. Planta, 228(4): 675-685.
[31] Yuan X, Huang P, Wang R Q, Li H Y, Lv X Q, Duan M, Tang H J, Zhang H S, Huang J. 2018. A zinc finger transcriptional repressor confers pleiotropic effects on rice growth and drought tolerance by down-regulating stress-responsive genes. Plant Cell Physiol, 59(10): 2129-2142.
[32] Zhang C L, Hu X, Zhang Y L, Liu Y, Wang G L, You C X, Li Y Y, Hao Y J. 2020a. An apple long-chain acyl-CoA synthetase 2 gene enhances plant resistance to abiotic stress by regulating the accumulation of cuticular wax. Tree Physiol, 40(10): 1450-1465.
[33] Zhang C L, Zhang Y L, Hu X, Xiao X, Wang G L, You C X, Li Y Y, Hao Y J. 2020b. An apple long-chain acyl-CoA synthetase, MdLACS4, induces early flowering and enhances abiotic stress resistance in Arabidopsis. Plant Sci, 297: 110529.
[34] Zhang D, Yang H F, Wang X C, Qiu Y J, Tian L H, Qi X Q, Qu L Q. 2020. Cytochrome P450 family member CYP96B5 hydroxylates alkanes to primary alcohols and is involved in rice leaf cuticular wax synthesis. New Phytol, 225(5): 2094-2107.
[35] Zhong M S, Jiang H, Cao Y, Wang Y X, You CX, Li Y Y, Hao Y J. 2020. MdCER2 conferred to wax accumulation and increased drought tolerance in plants. Plant Physiol Biochem, 149: 277-285.
Outlines

/

浙ICP备05004719号-15   公安备案号:33010302003355
Copyright © Editorial office of Rice Science
Tel: 0571-63371017 E-mail: crrn@fy.hz.zn.cn; cjrs278@gmail.com
Supported by Beijing Magtech Co., Ltd.
Total visitors:  Visitors of today:  Now online: