DOI QR코드

DOI QR Code

Molecular Cloning and Expression of a Cu/Zn-Containing Superoxide Dismutase from Thellungiella halophila

  • Xu, Xiaojing (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Zhou, Yijun (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Wei, Shanjun (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Ren, Dongtao (State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University) ;
  • Yang, Min (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Bu, Huahu (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Kang, Mingming (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Wang, Junli (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities) ;
  • Feng, Jinchao (Department of Biological Sciences, College of Life and Environmental Sciences, Central University for Nationalities)
  • 투고 : 2008.12.18
  • 심사 : 2009.02.26
  • 발행 : 2009.04.30

초록

Superoxide dismutases (SODs) constitute the first line of cellular defense against oxidative stress in plants. SODs generally occur in three different forms with Cu/Zn, Fe, or Mn as prosthetic metals. We cloned the full-length cDNA of the Thellungiella halophila Cu/Zn-SOD gene ThCSD using degenerate RT-PCR and rapid amplification of cDNA ends (RACE). Sequence analysis indicated that the ThCSD gene (GenBank accession number EF405867) had an open reading frame of 456 bp. The deduced 152-amino acid polypeptide had a predicted molecular weight of 15.1 kDa, an estimated pI of 5.4, and a putative Cu/Zn-binding site. Recombinant ThCSD protein was expressed in Escherichia coli and assayed for SOD enzymatic activity in a native polyacrylamide gel. The SOD activity of ThCSD was inactivated by potassium cyanide and hydrogen peroxide but not by sodium azide, confirming that ThCSD is a Cu/Zn-SOD. Northern blotting demonstrated that ThCSD is expressed in roots, stems, and leaves. ThCSD mRNA levels increased by about 30-fold when plants were treated with sodium chloride (NaCl), abscisic acid (ABA), and indole-acetic acid (IAA) and by about 50-fold when treated with UVB light. These results indicate that ThCSD is involved in physiological pathways activated by a variety of environmental conditions.

키워드

과제정보

연구 과제 주관 기관 : China Agricultural University

참고문헌

  1. Alscher, R.G., Erturk, N., and Heath, L.S. (2002). Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. J. Exp. Bot. 53, 1331-1341 https://doi.org/10.1093/jexbot/53.372.1331
  2. Bannister, J.V., Bannister, W.H., and Rottilio, G. (1987). Aspects of the structure, function and application of superoxide dismutases. Crit. Rev. Biochem. 22, 111-180 https://doi.org/10.3109/10409238709083738
  3. Bassman, J.H., Robberecht, R., and Edwards, G.E. (2001). Effects of enhanced UV-B radiation on growth and gas exchange in Populus deltoides Bartr. X Marsh. Int. J. Plant Sci.162, 103-110 https://doi.org/10.1086/317901
  4. Beem, K.M., Rich, W.E., and Rajagopalan, K.V. (1974). Total reconstitution of copper-zinc superoxide dismutase. J. Biol. Chem. 249, 7298-7305
  5. Bowler, C., Van Montagu, M., and Inze, D. (1992). Superoxide dismutase and stress tolerance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 43, 83-116 https://doi.org/10.1146/annurev.pp.43.060192.000503
  6. Bueno, P., Varela, J., Gimeenez-Gallego, G., and del Rio, L.A. (1995). Peroxisomal copper, zinc superoxide dismutase: characterization of the isoenzyme from watermelon cotyledons. Plant Physiol. 108, 1151-1160 https://doi.org/10.1104/pp.108.3.1151
  7. Cadenas, E. (1989). Biochemistry of oxygen toxicity. Annu. Rev. Biochem. 58, 79-110 https://doi.org/10.1146/annurev.bi.58.070189.000455
  8. Cannon, R.E., and Scandalios, J.G. (1989). Two cDNA encode two nearly identical Cu/Zn-SOD superoxide dismutase proteins in maize. Mol. Gen. Genet. 219, 1-8 https://doi.org/10.1007/BF00261150
  9. Choi, S.M., Jeong, S.W., Jeong, W.J., Kwon, S.Y., Chow, W.S., and Park, Y.I. (2002). Chloroplast Cu/Zn-superoxide dismutase is a highly sensitive site in cucumber leaves chilled in the light. Planta 216, 315-324 https://doi.org/10.1007/s00425-002-0852-z
  10. Chu, C.C., Lee, W.C., Guo, W.Y., Pan, S.M., Chen, L.J., Li, H.M., and Jinn, T.L. (2005). A copper Chaperone for superoxide dismutase that confers three types of copper/zinc superoxide dismutase activity in Arabidopsis. Plant Physiol. 139, 425-436 https://doi.org/10.1104/pp.105.065284
  11. Church, G., and Gilbert, W. (1984). Genomic sequencing. Proc. Natl. Acad. Sci. USA 81, 1991-1995 https://doi.org/10.1073/pnas.81.7.1991
  12. Deng, H.X., Hentati, A., Tainer, J.A., Iqbal, Z., Cayabyab, A., Hung, W.Y., Getzoff, E.D., Hu, P., Herzfeldt, B., Roos, R.P., et al. (1993). Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science 261, 1047-1051 https://doi.org/10.1126/science.8351519
  13. Desikan, R., Wood, L.G., Coffey, M.J., and Neill, S.J. (1996). Generation of active oxygen in elicited cells of Arabidopsis thaliana is mediated by a NADPH oxidase-like enzyme. FEBS Lett. 382, 231-217 https://doi.org/10.1016/0014-5793(96)00177-9
  14. Fridovich, I. (1986). Superoxide dismutases. Adv. Enzymol. 58, 61-97
  15. Gupta, A.S., Heinen, J.L., Holaday, A.S., Burke, J.J., and Allen, R.D. (1993). Increased resistance to oxidative stress in transgenic plants that overexpress chloroplastic Cu/Zn superoxide dismutase. Proc. Natl. Acad. Sci. USA 90, 1629-1633 https://doi.org/10.1073/pnas.90.4.1629
  16. Halliwell, B., and Gutteridge, J.M.C. (1999). Free radicals in biology and medicine, 3rd eds., (Oxford, UK: Oxford University Press)
  17. Herouant, D., Montagu, M.V., and Inze, D. (1993). Redox-activated expression of the cytosolic copper/zinc superoxide dismutase gene in Nicotiana. Proc. Natl. Acad. Sci. USA 90, 3108-3112 https://doi.org/10.1073/pnas.90.7.3108
  18. Inan, G., Zhang, Q., Li, P.H, Wang, Z.L, Cao, Z.Y, Zhang, H., Zhang, C., Quist, T.M., Goodwin, S.M., Zhu, J., et al. (2004). Salt cress. A halophyte and cryophyte Arabidopsis relative model system and its applicability to molecular genetic analyses of growth and development of extremophiles. Plant Physiol. 135, 1718-1737 https://doi.org/10.1104/pp.104.041723
  19. Jordan, B.R. (2002). Molecular response of plant cells to UV-B stress. Funct. Plant Biol. 29, 909-916 https://doi.org/10.1071/FP02062
  20. Jordan, B.R., James, P., and A-H-Mackerness, S. (1998). Factors affecting UV-B induced changes in Arabidposis thaliana gene expression: role of development, protective pigments and the chloroplast signal. Plant Cell Physiol. 39, 769-778 https://doi.org/10.1093/oxfordjournals.pcp.a029433
  21. Juarez, J.C., Manuia, M., Burnett, M.E., Betancourt, O., Boivin, B., Shaw, D.E., Tonks, N.K., Mazar, A.P., and Donate, F. (2008). Superoxide dismutase 1 (SOD1) is essential for $H_2O_2$-mediated oxidation and inactivation of phosphatases in growth factor signaling. Proc. Natl. Acad. Sci. USA 105, 7147-7152 https://doi.org/10.1073/pnas.0709451105
  22. Kanematsu, S., and Asada, K. (1989). Cu/Zn-superoxide dismutase in rice: occurrence of an active, monomeric enzyme and two types of isozyme in leaf and non-photosynthetic tissues. Plant Cell Physiol. 30, 381-391
  23. Kanematsu, S., and Asada, K. (1990). Characteristic amino acid sequences of chloroplast and cytosol isozymes of CuZnsuperoxide dismutase in spinach, rice and horsetail. Plant Cell Physiol. 31, 99-112
  24. Kernodle, S.P., and Scandalios, J.G. (1996). A comparison of the structure and function of the highly homologous maize antioxidant Cu/Zn superoxide dismutase genes, SOD4 and SOD4A. Genetics 144, 317-328
  25. Kliebenstein, D.J., Monde, R.A., and Last, R.L. (1998). Superoxide dismutase in Arabidopsis: an eclectic enzyme family with disparate regulation and protein localization. Plant Physiol. 118, 637-650 https://doi.org/10.1104/pp.118.2.637
  26. Kurepa, J.D., Herouart, D., Montagu, M.V., and Inze, D. (1997). Differential expression of Cu/Zn- and Fe-superoxide dismutase genes of tobacco during development, oxidative stress, and hormonal treatments. Plant Cell Physiol. 38, 463-470 https://doi.org/10.1093/oxfordjournals.pcp.a029190
  27. Kwon, S.I., and An, C.S. (2003). Cloning and expression of mitochondrial MnSOD from the small radish (Raphanus sativus L.). Mol. Cells 16, 194-200
  28. Laemmli, U.K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680-685 https://doi.org/10.1038/227680a0
  29. Lin, C.T., Yeh, K.W., Kao, M.C., and Shaw, J.F. (1993). Cloning and characterization of a cDNA encoding the cytosolic copper/zincsuperoxide dismutase from sweet potato tuberous root. Plant Mol. Biol. 23, 911-913 https://doi.org/10.1007/BF00021547
  30. Liu, A.R., Zhang, Y.B., and Chen, D.K. (2006). Effects on the growth of Thellungiella halophila and activity of antioxidative enzymes under salt stress. Plant Res. 26, 216-221
  31. Lo, M., Taylor, C., Wang, L., Nowack, L., Wang T. W., and Thompson, J. (2004). Characterization of an Ultraviolet B-Induced Lipase in Arabidopsis. Plant Physiol. 135, 947-958 https://doi.org/10.1104/pp.103.036376
  32. McCord, J.M., and Fridovich, I. (1969). Superoxide dismutase: an enzymatic function for erythrocuprein (hemocuprein). J. Biol. Chem. 244, 6049-6055
  33. Moran, J.F., James, E.K., Rubio, M.C., Sarath, G., Klucas, R.V., and Becana, M. (2003). Functional characterization and expression of a cytosolic iron-superoxide dismutase from cowpea root nodules. Plant Physiol. 133, 773-782 https://doi.org/10.1104/pp.103.023010
  34. Perl, A., Perl-Treves, R., Galili, S., Aviv, D., Shalgi, E., Malkin, S., and Galun, E. (1993). Enhanced oxidative stress defence in transgenic potato expressing tomato Cu,Zn superoxide dismutases. Theor. Appl. Genet. 85, 568-576 https://doi.org/10.1007/BF00220915
  35. Perl-Treves, R., and Galun, E. (1991). The tomato Cu, Zn superoxide dismutase genes are developmentally regulated and respond to light and stress. Plant Mol. Biol. 17, 745-760
  36. Perl-Treves, R., Abu-Abied, M., Magal, N., Galun, E., and Zamir, D. (1990). Genetic mapping of tomato cDNA clones encoding the chloroplastic and the cytosolic isozymes of superoxide dismutase. Biochem. Genet. 28, 543-552 https://doi.org/10.1007/BF00554381
  37. Pitcher, L.H., Brennan, E., Hurley, A., Dunsmuir, P., Tepperman, J.M., and Zilinskas, B.A. (1991). Overproduction of petunia chloroplastic copper/zinc superoxide dismutase does not confer ozone tolerance in transgenic tobacco. Plant Physiol. 97, 452-455 https://doi.org/10.1104/pp.97.1.452
  38. Pitcher, L.H., and Zilinskas, B.A. (1996). Overexpression of copper/ zinc superoxide dismutase in the cytosol of transgenic tobacco confers partial resistance to ozone-induced foliar necrosis. Plant Physiol. 110, 583-588 https://doi.org/10.1104/pp.110.2.583
  39. Rubio, M.C., Ramos, J., Webb, K.J., Minchin, F.R., Gonzalez, E., Arrese-Igor, C., and Becana, M. (2001). Expression studies of superoxide dismutases in nodules and leaves of transgenic alfalfa reveal abundance of iron-containing isozymes, posttranslational regulation, and compensation of isozymes activities. Mol. Plant-Microbe Interact. 14, 1178-1188 https://doi.org/10.1094/MPMI.2001.14.10.1178
  40. Sakamoto, A., Okumura, T., Kaminaka, H., Sumi, K., and Tanaka, K. (1995). Structure and differential response to abscisic acid of two promoters for the cytosolic copper/zinc superoxide dismutase genes. SodCc1 and SodCc2, in rice protoplast. FEBS Lett. 358, 62-66 https://doi.org/10.1016/0014-5793(94)01396-I
  41. Scandalios, J.G. (1997). Molecular genetics of superoxide dismutase in plants in oxidative stress and the molecular biology of antioxidant defenses, (Cold Spring Harbor, NY, USA: Cold Spring Harbor Laboratory Press)
  42. Scioli, J.R., and Zilinskas, B.A. (1988). Cloning and characterization of a cDNA encoding the chloroplastic copper/zinc-superoxide dismutase from pea. Proc. Natl. Acad. Sci. USA 85, 7661-7665 https://doi.org/10.1073/pnas.85.20.7661
  43. Stewart, R.R.C., and Bewley, J.D. (1980). Lipid peroxidation associated with accelerate aging of soybean axes. Plant Physiol. 65, 245-248 https://doi.org/10.1104/pp.65.2.245
  44. Tainer, J.A., Getzoff, E.D., Richardson, J.S., and Richardson, D.C. (1983). Structure and mechanism of copper, zinc superoxide dismutase. Nature 306, 284-287 https://doi.org/10.1038/306284a0
  45. Taji, T., Seki, M., Satou, M., Sakurai, T., Kobayashi, M., Ishiyama, K., Narusaka, Y., Narusaka, M., Zhu, J., and Shinozaki, K. (2004). Comparative genomics in salt tolerance between Arabidopsis and Arabidopsis-related halophyte salt cress using Arabidopsis microarray. Plant Physiol. 135, 1697-709 https://doi.org/10.1104/pp.104.039909
  46. Tang, L., Kwon, S.Y., and Kim, S.H. (2006). Enhanced tolerance of transgenic potato plants expressing both superoxide dismutase and ascorbate peroxidase in chloroplasts against oxidative stress and high temperature. Plant Cell Rep. 25, 1380-1386 https://doi.org/10.1007/s00299-006-0199-1
  47. Towbin, H., Staehelin, T., and Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc. Nat. Acad. Sci. USA 76, 4350-4354 https://doi.org/10.1073/pnas.76.9.4350
  48. Tsang Ed, W.T., Bowler, C., Herouart, D., Van Camp, W., Villaroel, R., Genetello, C., Van Montagu, M., and Inze, D. (1991). Differential regulation of superoxide dismutase in plants exposed to environmental stress. Plant Cell 3, 783-792 https://doi.org/10.1105/tpc.3.8.783
  49. Wang, Z.L., Li, P.H., Fredricksen, M., Gong, Z.Z., Kim, C.S., Zhang, C.Q., Bohnert, H.J., Zhu, J.K., Bressan, R.A., Hasegawa, P.M., et al. (2004). Expressed sequence tags from Thellungiella halophila, a new model to study plant salt-tolerance. Plant Sci. 166, 609-616 https://doi.org/10.1016/j.plantsci.2003.10.030
  50. Wong, C.E., Li, Y., Whitty, B.R., Diaz-Camino, C., Akhter, S.R., Brandle, J.E., Golding, G.B., Weretilnyk, E.A., Moffatt, B.A., and Griffith, M. (2005). Expressed sequence tags from the Yukon ecotype of Thellungiella salsuginea reveal that gene expression in response to cold, drought and salinity shows little overlap. Plant Mol. Biol. 58, 561-574 https://doi.org/10.1007/s11103-005-6163-6
  51. Wu, G., Wilen, R.W., Robertson, A.J., and Gusta, L.V. (1999). Isolation, chromosomal localization and differential expression of mitochondrial manganese superoxide dismutase and chloroplastic copper/zinc superoxide dismutase genes in wheat. Plant Physiol. 120, 513-520 https://doi.org/10.1104/pp.120.2.513
  52. Yamaguchi-Shinozaki, K., and Shinozaki, K. (1994). A novel cisacting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress. Plant Cell 6, 251-264 https://doi.org/10.1105/tpc.6.2.251
  53. Zhao, K.F., and Li, F.Z. (1999). Salt plants in China. (Beijing, China: Science Press)
  54. Zhu, J.K. (2001). Plant salt tolerance. Trends Plant Sci. 6, 66-71 https://doi.org/10.1016/S1360-1385(00)01838-0

피인용 문헌

  1. Cloning, overexpression, purification, and characterization of a new iron superoxide dismutase fromJatropha curcas : The study of Fe-SOD from J. curcas vol.59, pp.5, 2009, https://doi.org/10.1002/bab.1030
  2. High-level expression of a sika deer (Cervus nippon) Cu/Zn superoxide dismutase in Pichia pastoris and its characterization vol.35, pp.2, 2009, https://doi.org/10.1016/j.etap.2012.11.013
  3. Cloning and characterization of gene encoding a Mn-containing superoxide dismutase in Eutrema halophilum vol.58, pp.1, 2014, https://doi.org/10.1007/s10535-013-0363-8
  4. Global Analysis of Gene Expression Profiles in Physic Nut ( Jatropha curcas L.) Seedlings Exposed to Salt Stress vol.9, pp.5, 2014, https://doi.org/10.1371/journal.pone.0097878
  5. The Functional and Regulatory Mechanisms of the Thellungiella salsuginea Ascorbate Peroxidase 6 (TsAPX6) in Response to Salinity and Water Deficit Stresses vol.11, pp.4, 2009, https://doi.org/10.1371/journal.pone.0154042
  6. Overexpression of the ABC transporter gene TsABCG11 increases cuticle lipids and abiotic stress tolerance in Arabidopsis vol.12, pp.5, 2018, https://doi.org/10.1007/s11816-018-0495-6
  7. Effects of UV-B radiation on the survival, egg hatchability and transcript expression of antioxidant enzymes in a high-temperature adapted strain of Neoseiulus barkeri vol.77, pp.4, 2019, https://doi.org/10.1007/s10493-019-00361-9