Influencing factors of genetic transformation efficiency in tobacco (Nicotiana tabacum ‘NC89')using Agrobacterium tumefacience

Samaneh Sadat MALEKI, Kourosh MOHAMMADI, Kongshu JI

JOURNAL OF NANJING FORESTRY UNIVERSITY ›› 2018, Vol. 42 ›› Issue (01) : 27-34.

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JOURNAL OF NANJING FORESTRY UNIVERSITY ›› 2018, Vol. 42 ›› Issue (01) : 27-34. DOI: 10.3969/j.issn.1000-2006.201705030

Influencing factors of genetic transformation efficiency in tobacco (Nicotiana tabacum ‘NC89')using Agrobacterium tumefacience

  • Samaneh Sadat MALEKI, Kourosh MOHAMMADI, Kongshu JI*
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Abstract

【Objective】 In this study, we aim to report the production of transgenic tobacco ‘NC89' using Agrobacterium tumefaciens harboring the PBI121:CslA1 binary vector and the optimization of some transformation parameters to enhance transformation efficiency. 【Method】 By optimizing the Murashige and Skoog medium enriched with 6-BA(2.0 mg/L)and NAA(0.1 mg/L), we got a large number of seeding for subsequent usage and achieved the maximum number of shoots per explant. To find out the most effective condition for tobacco transformation, we examined some parameters, including the Agrobacterium concentration, pre-culture duration, Agrobacterium infection duration, co-culture period, treatment of selective media containing kanamycin and dark incubation in selective duration. Transgenic seedlings was obtained by controlling some transformation parameters including the Agrobacterium concentration, pre-culture duration, Agrobacterium transformation duration, co-culture period, to complete selection with media containing kanamycin. 【Result】 The highest transformation efficiency was obtained with two days of explant pre-culture, Agrobacterium concentration of D600 being 0.7, Agrobacterium inoculation for 20 min. The appropriate concentration of kanamycin at the concentration of 100 mg/L was applied to screen transformed cells, and dark incubation for four days during co-cultivation increased the regeneration rate. Incubation for seven days in darkness after changing the selective medium shortened the callus induction duration. Putative transformants were verified by RT-PCR and Southern blot hybridization. 【Conclusion】 The present study achieved the overexpression of transgenes in tobacco and increased the transformation efficiency through optimizing conditions of the several key steps in gene transformation. This Agrobacterium-mediated transformation protocol could help a lot for the genetic application of A. tumefaciens mediated transformation in Nicotiana tabacum and related species.

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Samaneh Sadat MALEKI, Kourosh MOHAMMADI, Kongshu JI. Influencing factors of genetic transformation efficiency in tobacco (Nicotiana tabacum ‘NC89')using Agrobacterium tumefacience[J]. JOURNAL OF NANJING FORESTRY UNIVERSITY. 2018, 42(01): 27-34 https://doi.org/10.3969/j.issn.1000-2006.201705030

References

[1] GANAPATHI T R,SUPRASANNA P,RAO P S, et al. Tobacco(Nicotiana tabacum L.): a model system for tissue culture interventions and genetic engineering[J]. Indian Journal of Biotechnology,2004(3):171-184.
[2] VASIL V,HILDEBRANDT A C. Differentiation of tobacco plants from single,isolated cells in microcultures[J]. Science,1965,150(3698): 889-892. DOI:10.1126/science.150.3698.889.
[3] HORSCH R B,FRY J E,HOFFMAN N L,et al. A simple and general method for transferring genes into plants[J]. Science,1985,227(4691): 1229-1231. DOI:10.1126/science.227.4691.1229.
[4] FRALEY R T,ROGERS S G,HORSCH R B,et al. Genetic transformation in higher plants[J]. Critical Reviews in Plant Sciences,1986,4(1): 1-46. DOI:10.1080/07352688609382217.
[5] AN G. High efficiency transformation of cultured tobacco cells[J]. Plant Physiol,1985,79(2): 568-570. DOI:10.1104/pp.79.2.568.
[6] GALLOIS P,MARINHO P. Leaf disk transformation using Agrobacterium tumefaciens-expression of heterologous genes in tobacco[J]. Methods Mol Biol,1995,49: 39-48. DOI:10.1385/0-89603-321-X:39.
[7] TZFIRA T,LI J,LACROIX B,et al. Agrobacterium T-DNA integration: molecules and models[J]. Trends Genet,2004,20(8): 375-383. DOI:10.1016/j.tig.2004.06.004.
[8] GELVIN S B.Agrobacterium-mediated plant transformation: the biology behind the “Gene-Jockeying” tool [J]. Microbiology and Molecular Biology Reviews,2003,67(1): 16-37. DOI:10.1128/mmbr.67.1.16-37.2003.
[9] VELUTHAMBI K,GUPTA A K,SHARMA A. The current status of plant transformation technologies [J]. Current Science,2003,84(3):368-380.
[10] KOMARI T,ISHIDA Y,HIEI Y. Plant transformation technology:Agrobacterium-mediated transformation[G]// Handbook of Plant Biotechnology,2004(1):223-261. DOI:10.1002/0470869143.kc014.
[11] SHOU H, FRAME B R, WHITHAM S A,et al. Assessment of transgenic maize events produced by particle bombardment or Agrobacterium-mediated transformation [J]. Molecular Breeding, 2004, 13(2):201-208.
[12] GOUBET F, BARTON, C J, MORTIMER J C, et al. Cell wall glucomannan in Arabidopsis is synthesised by CSLA glycosyltransferases, and influences the progression of embryogenesis[J]. The Plant Journal, 2009, 60, 527-538. DOI: 10.1111/j.1365-313X.2009.03977.x.
[13] HOLSTERS M,DE WAELE D,DEPICKER A,et al. Transfection and transformation of Agrobacterium tumefaciens[J]. Mol Gen Genet,1978,163(2): 181-187. DOI:10.1007/bf00267408.
[14] HORSCH R B,FRY J,HOFFMANN N,et al. Leaf disc transformation[C]// GELVIN S B, SCHIPEROORT R A. Plant molecular biology manual, Netherlauds: Kluwer Academic Publishers, 1988:63-71.
[15] DOYLE J J,DICKSON E E. Preservation of plant samples for DNA restriction endonuclease analysis[J]. Taxon,1987,36(4): 715. DOI:10.2307/1221122.
[16] POREBSKI S,BAILEY L G,BAUM B R. Modification of a CTAB DNA extraction protocol for plants containing high polysaccharide and polyphenol components[J]. Plant Molecular Biology Reporter,1997,15(1): 8-15. DOI:10.1007/bf02772108.
[17] STOLARZ A,MACEWICZ J,LÖRZ H. Direct somatic embryogenesis and plant regeneration from leaf explants of Nicotiana tabacum L.[J]. Journal of Plant Physiology,1991,137(3): 347-357. DOI:10.1016/s0176-1617(11)80144-6.
[18] SKOOG F,MILLER C O. Chemical regulation of growth and organ formation in plant tissues cultured in vitro[J]. Symp Soc Exp Biol,1957,11: 118-130.
[19] SONG G Q,HONDA H,YAMAGUCHI K I. Efficient Agrobacterium tumefaciens-mediated transformation of sweet potato(Ipomoea batatas (L.)Lam.)from stem explants using a two-step kanamycin-hygromycin selection method[J]. In Vitro Cellular & Developmental Biology-Plant,2004,40(4): 359-365. DOI:10.1079/ivp2004539.
[20] HAN SN, O H P R, KIM H S, et al. Effects of antibiotics on suppression of Agrobacterium tumefaciens and plant regeneration from wheat embryo [J]. Crop Science and Biotechnology, 2007, 10(2): 92-98.
[21] KONDO T,HASEGAWA H,SUZUKI M. Transformation and regeneration of garlic(Allium sativum L.)by Agrobacterium-mediated gene transfer[J]. Plant Cell Reports,2000,19(10): 989-993. DOI:10.1007/s002990000222.
[22] ZHANG K,LETHAM D S,JOHN P C. Cytokinin controls the cell cycle at mitosis by stimulating the tyrosine dephosphorylation and activation of p34cdc2-like H1 histone kinase[J]. Planta,1996,200(1): 2-12. DOI:10.1007/bf00196642.
[23] KIEBER J J,SCHALLER G E. Cytokinins[J]. The Arabidopsis Book,2014,12: e0168. DOI:10.1199/tab.0168.
[24] DAVIES P J. The plant hormones: their nature,occurrence,and functions [G]// DAVIES P. Plant hormones. Netherlands: Springer,2010: 1-15. DOI:10.1007/978-1-4020-2686-7_1.
[25] KIM M J,KIM J K,KIM H J,et al. Genetic modification of the soybean to enhance the β-carotene content through seed-specific expression[J]. PLoS One,2012,7(10): e48287. DOI:10.1371/journal.pone.0048287.
[26] ISHIDA J K,YOSHIDA S,ITO M,et al. Agrobacterium rhizogenes-mediated transformation of the parasitic plant Phtheirospermum japonicum[J]. PLoS One,2011,6(10): e25802. DOI:10.1371/journal.pone.0025802.
[27] HAN J L,WANG H,YE H C,et al. High efficiency of genetic transformation and regeneration of Artemisia annua L. via Agrobacterium tumefaciens-mediated procedure[J]. Plant Science,2005,168(1): 73-80. DOI:10.1016/j.plantsci.2004.07.020.
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