GmFAD3A, A ω-3 fatty acid desaturase gene, enhances cold tolerance and seed germination rate under low temperature in rice

International Journal of Molecular Sciences

Volumn 20, Issue 15, 2019, Pages

  Wang, Xin ^a   Yu, Chao ^a   Liu, Yi ^a   Yang, Lu ^a   Li, Yang ^b   Yao, Wen ^b   Cai, Yicong ^c   Yan, Xin ^a   Li, Shaobo ^a   Cai, Yaohui ^d   Li, Shaoqing ^e   Peng, Xiaojue ^a  

^a NANCHANG UNIVERSITY   (China)

^b HENAN AGRICULTURAL UNIVERSITY   (China)

^c JIANGXI AGRICULTURAL UNIVERSITY   (China)

^d Jiangxi Super rice Research and Development Center   (China)

^e WUHAN UNIVERSITY   (China)

Author keywords

Cold stress; GmFAD3A; Oryza sativa; Seed germination; 3 fatty acid desaturase

Indexed keywords

ACYL COENZYME A DESATURASE; ARACHIDIC ACID; CATALASE; HYDROPEROXIDASE; HYGROMYCIN; LINOLENIC ACID; MALONALDEHYDE; OLEIC ACID; OMEGA 3 FATTY ACID; PALMITIC ACID; PEROXIDASE; POLYUNSATURATED FATTY ACID; PROLINE; REACTIVE OXYGEN METABOLITE; STEARIC ACID; SUPEROXIDE DISMUTASE; UBIQUITIN; UNCLASSIFIED DRUG; OMEGA-3 FATTY ACID DESATURASE;

A GENE; AGROBACTERIUM TUMEFACIENS; ARTICLE; CELL TRANSFORMATION; COLD SENSITIVITY; COLD STRESS; COLD TOLERANCE; CONTROLLED STUDY; ECTOPIC EXPRESSION; ENVIRONMENTAL STRESS; ENZYME ACTIVITY; ESCHERICHIA COLI; GENE OVEREXPRESSION; GENETIC TRANSFORMATION; GERMINATION; GMFAD3A GENE; GROWTH RATE; LOW TEMPERATURE; NONHUMAN; OXIDATION; PHENOTYPE; PHYLOGENY; PLANT GROWTH; PLANT HEIGHT; PRODUCTIVITY; REAL TIME POLYMERASE CHAIN REACTION; RICE; RISK FACTOR; RNA ISOLATION; SEED HUSK; SEQUENCE ANALYSIS; SOYBEAN; SURVIVAL RATE; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; LIPID METABOLISM; ORYZA; PHYSIOLOGICAL STRESS; PLANT LEAF; PLANT SEED; SEEDLING; TRANSGENIC PLANT;

CATALASE; FATTY ACID DESATURASES; GENE EXPRESSION REGULATION, PLANT; GERMINATION; LIPID METABOLISM; ORYZA; PEROXIDASE; PLANT LEAVES; PLANTS, GENETICALLY MODIFIED; SEEDLINGS; SEEDS; SOYBEANS; STRESS, PHYSIOLOGICAL; SUPEROXIDE DISMUTASE;

EID: 85071157450     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms20153796     Document Type: Article

References (32)

1. Wang, X.; Zhou, W.; Lu, Z.; Ouyang, Y.; Yao, J. A lipid transfer protein, OsLTPL36, is essential for seed development and seed quality in rice. Plant Sci. 2015, 239, 200–208. [CrossRef] [PubMed]
2. Endo, T.; Chiba, B.; Wagatsuma, K.; Saeki, K.; Ando, T.; Shomura, A.; Mizubayashi, T.; Ueda, T.; Yamamoto, T.; Nishio, T. Detection of QTLs for cold tolerance of rice cultivar ‘Kuchum’ and effect of QTL pyramiding. Theor. Appl. Genet. 2016, 129, 631–640. [CrossRef] [PubMed]
3. Eremina, M.; Rozhon, W.; Poppenberger, B. Hormonal control of cold stress responses in plants. Cell Mol. Life Sci. 2016, 73, 797–810. [CrossRef] [PubMed]
4. Liu, Y.; Xu, C.; Zhu, Y.; Zhang, L.; Chen, T.; Zhou, F.; Chen, H.; Lin, Y. The calcium-dependent kinase OsCPK24 functions in cold stress responses in rice. J. Integr. Plant Biol. 2018, 60, 173–188. [CrossRef] [PubMed]
5. Beney, L.; Gervais, P. Influence of the fluidity of the membrane on the response of microorganisms to environmental stresses. Appl. Microbiol. Biotechnol. 2001, 57, 34–42. [PubMed]
6. Dyer, J.M.; Mullen, R.T. Engineering plant oils as high-value industrial feedstocks for biorefining: The need for underpinning cell biology research. Physiol. Plant 2008, 132, 11–22. [CrossRef] [PubMed]
7. Zhou, Z.; Wang, M.J.; Zhao, S.T.; Hu, J.J.; Lu, M.Z. Changes in freezing tolerance in hybrid poplar caused by up-and down-regulation of PtFAD2 gene expression. Transgenic Res. 2010, 19, 647–654. [CrossRef] [PubMed]
8. Los, D.A.; Murata, N. Membrane fluidity and its roles in the perception of environmental signals. Biochim Biophys. Acta 2004, 1666, 142–157. [CrossRef] [PubMed]
9. Ishizaki-Nishizawa, O.; Fujii, T.; Azuma, M.; Sekiguchi, K.; Murata, N.; Ohtani, T.; Toguri, T. Low-temperature resistance of higher plants is significantly enhanced by a nonspecific cyanobacterial desaturase. Nat. Biotechnol 1996, 14, 1003–1006. [CrossRef]
10. Pham, A.T.; Shannon, J.G.; Bilyeu, K.D. Combinations of mutant FAD2 and FAD3 genes to produce high oleic acid and low linolenic acid soybean oil. Theor. Appl. Genet. 2012, 125, 503–515. [CrossRef]
11. Schmutz, J.; Cannon, S.B.; Schlueter, J.; Ma, J.; Mitros, T.; Nelson, W.; Hyten, D.L.; Song, Q.; Thelen, J.J.; Cheng, J.; et al. Genome sequence of the palaeopolyploid soybean. Nature 2010, 463, 178–183. [CrossRef]
12. Rajwade, A.V.; Kadoo, N.Y.; Borikar, S.P.; Harsulkar, A.M.; Ghorpade, P.B.; Gupta, V.S. Differential transcriptional activity of SAD, FAD2 and FAD3 desaturase genes in developing seeds of linseed contributes to varietal variation in alpha-linolenic acid content. Phytochemistry 2014, 98, 41–53. [CrossRef] [PubMed]
13. Silva, L.C.C.; Bueno, R.D.; da Matta, L.B.; Pereira, P.H.S.; Mayrink, D.B.; Piovesan, N.D.; Sediyama, C.S.; Fontes, E.P.B.; Cardinal, A.J.; Dal-Bianco, M. Characterization of a new GmFAD3A allele in Brazilian CS303TNKCA soybean cultivar. Theor. Appl. Genet. 2018, 131, 1099–1110. [CrossRef] [PubMed]
14. Shimada, T.; Wakita, Y.; Otani, M.; Iba, K. Modification of Fatty Acid Composition in Rice Plants by Transformation with a Tobacco Microsomal omega;-3 Fatty Acid Desaturase Gene (NtFAD3). Plant Biotechnol. 2000, 17, 43–48. [CrossRef]
15. Anai, T.; Koga, M.; Tanaka, H.; Kinoshita, T.; Rahman, S.M.; Takagi, Y. Improvement of rice (Oryza sativa L.) seed oil quality through introduction of a soybean microsomal omega-3 fatty acid desaturase gene. Plant Cell Rep. 2003, 21, 988–992. [CrossRef] [PubMed]
16. Ying, J.Z.; Shan, J.X.; Gao, J.P.; Zhu, M.Z.; Shi, M.; Lin, H.X. Identification of quantitative trait Loci for lipid metabolism in rice seeds. Mol. Plant 2012, 5, 865–875. [CrossRef] [PubMed]
17. Varshney, R.K.; Bansal, K.C.; Aggarwal, P.K.; Datta, S.K.; Craufurd, P.Q. Agricultural biotechnology for crop improvement in a variable climate: Hope or hype? Trends Plant Sci. 2011, 16, 363–371. [CrossRef]
18. Wang, J.; Wang, J.; Wang, X.; Li, R.; Chen, B. Proteomic response of hybrid wild rice to cold stress at the seedling stage. PLoS ONE 2018, 13, e0198675. [CrossRef]
19. Liu, C.T.; Wang, W.; Mao, B.G.; Chu, C.C. Cold stress tolerance in rice: Physiological changes, molecular mechanism, and future prospects. Yi Chuan 2018, 40, 171–185.
20. Man, L.; Xiang, D.; Wang, L.; Zhang, W.; Wang, X.; Qi, G. Stress-responsive gene RsICE1 from Raphanus sativus increases cold tolerance in rice. Protoplasma 2017, 254, 945–956. [CrossRef]
21. Liu, W.X.; Liu, H.L.; Qu le, Q. Embryo-specific expression of soybean oleosin altered oil body morphogenesis and increased lipid content in transgenic rice seeds. Theor. Appl. Genet. 2013, 126, 2289–2297. [CrossRef]
22. Wang, H.S.; Yu, C.; Tang, X.F.; Wang, L.Y.; Dong, X.C.; Meng, Q.W. Antisense-mediated depletion of tomato endoplasmic reticulum omega-3 fatty acid desaturase enhances thermal tolerance. J. Integr. Plant Biol. 2010, 52, 568–577. [CrossRef] [PubMed]
23. Liu, H.L.; Yin, Z.J.; Xiao, L.; Xu, Y.N.; Qu le, Q. Identification and evaluation of omega-3 fatty acid desaturase genes for hyperfortifying alpha-linolenic acid in transgenic rice seed. J. Exp. Bot. 2012, 63, 3279–3287. [CrossRef]
24. Nishida, I.; Murata, N. CHILLING SENSITIVITY IN PLANTS AND CYANOBACTERIA: The Crucial Contribution of Membrane Lipids. Annu. Rev. Plant Biol. 1996, 47, 541–568. [CrossRef] [PubMed]
25. Cao, Y.P.; Shi, J.L.; Li, Z.; Ming, F. Isolation of OsFAD2, OsFAD6 and FAD family members response to abiotic stresses in Oryza sativa L. Yi chuan= Hereditas 2010, 32, 839–847. [CrossRef] [PubMed]
26. Wu, C.; Li, X.; Yuan, W.; Chen, G.; Kilian, A.; Li, J.; Xu, C.; Li, X.; Zhou, D.X.; Wang, S.; et al. Development of enhancer trap lines for functional analysis of the rice genome. Plant J. 2003, 35, 418–427. [CrossRef] [PubMed]
27. Berry, S. Lipid Analysis: Isolation, Separation, Identification and Structural Analysis of Lipids. Nutr. Bulletin 2010, 29, 72–73. [CrossRef]
28. Cruz-Hernandez, C.; Deng, Z.; Zhou, J.; Hill, A.R.; Yurawecz, M.P.; Delmonte, P.; Mossoba, M.M.; Dugan, M.E.; Kramer, J.K. Methods for analysis of conjugated linoleic acids and trans-18:1 isomers in dairy fats by using a combination of gas chromatography, silver-ion thin-layer chromatography/gas chromatography, and silver-ion liquid chromatography. J. AOAC Int. 2004, 87, 545–562.
29. Byun, M.Y.; Cui, L.H.; Lee, J.; Park, H.; Lee, A.; Kim, W.T.; Lee, H. Identification of Rice Genes Associated with Enhanced Cold Tolerance by Comparative Transcriptome Analysis with Two Transgenic Rice Plants Overexpressing DaCBF4 or DaCBF7, Isolated From Antarctic Flowering Plant Deschampsia antarctica. Front. Plant Sci. 2018, 9, 601. [CrossRef]
30. Wang, X.; Chen, J.; Liu, C.; Luo, J.; Yan, X.; Aihua, A.; Cai, Y.; Xie, H.; Ding, X.; Peng, X. Over-expression of a protein disulfide isomerase gene from Methanothermobacter thermautotrophicus, enhances heat stress tolerance in rice. Gene 2019, 684, 124–130. [CrossRef]
31. Landi, M. Commentary to: “Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds” by Hodges et al., Planta (1999) 207:604–611. Planta 2017, 245, 1067. [CrossRef] [PubMed]
32. Kaur, N.; Dhawan, M.; Sharma, I.; Pati, P.K. Interdependency of Reactive Oxygen Species generating and scavenging system in salt sensitive and salt tolerant cultivars of rice. BMC Plant Biol. 2016, 16, 131. [CrossRef] [PubMed]