Efficient transformation of potato stems segments from cultivar Désirée, using phosphinothricin as selection marker;Transformación eficiente de segmentos de tallos de papa de la variedad Désirée, utilizando fosfinotricina como marcador de selección

Biotecnologia Aplicada

Volumn 24, Issue 2, 2007, Pages 132-138

  Soto, Natacha ^a   Enríquez, Gil A ^a   Ferreira, Aleines ^a   Corrada, Miriel ^a   Fuentes, Alejandro ^a   Tiel, Kenia ^a   Pujol, Merardo ^a  

^a CENTER FOR GENETIC ENGINEERING AND BIOTECHNOLOGY   (Cuba)

Author keywords

Finale ; Genetic transformation; Herbicide resistance; Phosphinothricin; Potato; PPT

Indexed keywords

AMMONIUM DERIVATIVE; CHLOROPHENOL; HERBICIDE; PHOSPHINOTHRICIN;

ARTICLE; BAR GENE; GENE; GENE EXPRESSION; GENETIC TRANSFORMATION; GENOME; GREENHOUSE; NONHUMAN; PLANT LEAF; PLANT STEM; POLYMERASE CHAIN REACTION; POTATO; RHIZOBIUM RADIOBACTER; SHOOT; TRANSGENIC PLANT;

AGROBACTERIUM TUMEFACIENS; SOLANUM TUBEROSUM;

EID: 43649100328     PISSN: 08644551     EISSN: 10272852     Source Type: Journal    
DOI: None     Document Type: Article

References (48)

1. Enríquez G, Soto N, Doreste V, Hernán-dez L, Pérez M, Peral R, et al. Transformación genética de variedades comerciales de papa. Resultados de la biotecnología de la papa en Cuba. En: Ana Estévez (ed.). El cultivo de la papa en Cuba (2005):236-61.
2. Paredes E, Pérez E, García R, La O. Programa de manejo sostenible de malezas con el uso racional de herbicidas en el cultivo de la papa (1999).
3. Mulwa MR, Mwanza ML. Review: Biotechnology approaches to developing herbicide tolerance/selectivity in crops. African Journal of Biotechnology (2006); 5(5):396-404.
4. Ooms G, Burrell M, Karp A, Bevan M, HiIIe J. Genetic transformation in two potato cultivars with T-DNA from disarmed Agrobacterium. Theoretical and Applied Genetics (1987); 73:744-50.
5. Stiekema W, Heidekamp F, Louwerse J, Verhoeven H, Dijkhuis P. Introduction of foreing genes into potato cultivars Bintje and Désirée using an Agrobacterium tumefaciens binary vector. Plant Cell Report (1988); 7:47-50.
6. Hutchinson P, Dennos J, Beutler B. Efficacy and Economics of weed control programs in Glyphosate-Resistant potato (Solanum tuberosum). Weed Technol (2002); 17(4):854-65.
7. D'Halluin K, De Block M, Denecke J, Janssens J, Leemans J, Reynaerts A, et al. The bar gen as selectable and screenable marker in plant engineering. Methods In Enzymology. ed. Academic Press, NY; 1992.
8. Craig W, Gargano D, Scotti N, Nguyen TT, Lao NT, Kavanagh TA, et al. Direct gene transfer in potato: a comparison of particle bombardment of leaf explants and PEG-mediated transformation of protoplasts. Plant Cell Rep (2005); 24(10):603-11.
9. Lutz K, Knapp J, Maliga P. Expression of bar in the plastid genome confers herbicide resistance. Plant Physiol (2001); 125(4):1585-90.
10. De Block M, Botterman J, Vandewiele M, Dockx J, Thoen C, Gosselé V, et al. Engineering herbicide resistance in plants by expression of a detoxifying enzyme. EMBO J (1987); 6(9):2513-8.
11. Bayer Crop Science. Technical information Glufosinate-ammonium (2005); 38.
12. Thompson C, Movva N, Tizard R, Crameri R. Characterization of the herbicide-resistance gene bar from Streptomyces hygroscopicus. EMBO J (1987); 6:2519-23.
13. Díaz A, Lacuesta M, Muñoz-Rueda A. Comparative effects of phosphinothricin on nitrate and ammoniun assimilation and on anaplerotic CO2 fixation in N-deprived barley plants. J Plant Physiology (1996); 149:9-13.
14. De Block M. Genotype-independent leaf disc transformation in potato (Solanum tuberosum) using Agrobacterium tumefaciens. Theor Appl Genet (1988); 76:767-74.
15. Figueira E, Figueiredo L, Monte-Neshich D. Transformation of potato (Solanum tuberosum) cv. Mantiqueira using Agrobacterium tumefaciens and evaluation of herbicide resistance. Plant Cell Reports (1994); 13(12):666-70.
16. Sawahel W. Ultrasound-mediated stable transformation of potato tuber discs. Biotechnology Techniques (1996); 10(11):821-4.
17. Beaujean A, Sangwan R, Lecardonnel A, Sangwan-Norreel B. Agrobacterium mediated transformation of three economically important potato cultivars using sliced internodal explants: An efficient protocol of transformation. Journal of Experimental Botany (1998); 49(326):1589-95.
18. Visser R, Jacobsen E, Hesseling Meinders A, Schans M, Witholt B, Feenstra W. Transformation of homozygous diploid potato with an Agrobacterium tumefaciens binary vector system by adventicious shoot regeneration on leaf and stem segments. Plant Molecular Biology (1989); 12:329-37.
19. Romano A, Raemakers K, Visser R, Mooibroek H. Transformation of potato (Solanum tuberosum L.) using particle bombardment. Plant Cell Reports (2001); 20:198-204.
20. Enríquez G, Fuentes A, Selman Housein G, Téllez P, Soto N, Pérez M, et al. Effect of different culture methods on in vitro regeneration of potato (Solanum tuberosum L.) cv. Chieftain. Biotecnología Aplicada (1997); 14(3):181-4.
21. Murashige T, Skoog F. A revised medium for rapid growth and bioassay with tobacco tissue culture. Physiol Plant (1962); 15:473-9.
22. Millar J. Experiments in Molecular Genetics. NY; 1972.
23. Kramer C, Dimaio J, Carswell G, Shillito R. Selection of transformed protoplast-derived Zea mays colonies with phosphinotricin and a novel assay using the ph indicador chlorophenol red. Planta (1993); 190:454-8.
24. Dellaporta S, Wood J, Hicks B. A plant minipreparation: Version II. Plant Mol Biol Rep (1983); 4:19-21.
25. Takumi S, Shimada T. Production of transgenic wheat through particle bombardment of scutellar tissues: frequency is influenced by cultura duration. Plant Physiol (1996); 49:418-23.
26. Chang M, Culley D, Choi J, Hadwiger LA. Agrobacterium-mediated co-transformation of a pea basic chitinase and b-1-3-glucanase in potato(Solanum tuberosum L.cv. Russet Burbank) using a single selectable marker. Plant Science (2002); 163:83-9.
27. Gustafson V, Mallubhotla S, Mac Donnell J, Sanyal-Bagchi M, Chakravarty B, Wang-Pruski G. Transformation and Plant Regeneration from Leaf Explants of Solanum tuberosum L. cv. 'Shepody'. Plant Cell, Tissue and Organ Culture (2006); 85(3):361-6.
28. Rakosy-Tican L, Aurori C, Thieme R, Capdefien C, Aurori A, Antonova O. The usefulness of reporter gene gfp for optimizing Agrobacterium tumefaciens mediated transformation of potato cultivars. Biotechnol Agron Soc Environ (2003); 7(4):188-95.
29. M' Hamdi M, Rouviére C, Rojas-Beltrán J, Du Jardin P. Optimisation de la transformation génétique de la pomme de terre par Agrobacterium tumefaciens. Utilisation de la résistance a' hygromycine comme marqueur sélectif. Biotechnol Agron Soc Environ (2003); 3-4:183-8.
30. Newell C, Rozman R, Hinchee M, Lawson E, Haley L, Sanders P, et al. Agrobacterium-mediated transformation of Solanum tuberosum L. cv. Russet Burbank. Plant Cell Reports (1991); 10(1):30-34.
31. Ducreux L, Morris W, Taylor M, Millam S. Agrobacterium-mediated transformation of Solanum phurej. Plant Cell Report (2005); 24:10-4.
32. Banerjee A, Prat S, Hannapel A. Efficient production of transgenic potato (Solanum tuberosum L. ssp andigena) plant via Agrobacterium mediated transformation. Plant Science (2006); 170:1732-8.
33. Barrell P, Shang Youngjin, Cooper P, Conner A. Alternative selectable markers for potato transformation using minimal T-DNA vectors. Plant Cell, Tissue and Organ Culture (2002); 70:61-8.
34. Wenzler H, Mignery G, May G, Park W. A rapid and efficient transformation method for the production of large numbers of transgenic potato plants. Plant Science (1989); 63:79-85.
35. Trujillo C, Rodríguez-Arango E, Jaramillo S, Hoyos R, Orduz S, Arango R. One step transformation of two Andean potato cultivars (Solanum tuberosum L. subsp andigena). Plant Cell Reports (2001); 20:637-41.
36. JayaSree T, Pavan U, Ramesh M, Rao A, Jagan Mohan Reddy K, Sadanandam A. Somatic embryogenesis from leaf cultures of potato. Plant Cell, Tissue and Organ Culture (2001); 64:13-7.
37. Hulme J, Higgins E, Shields R. An efficient genotype independent method for regeneration of potato plants from leaf tissue. Plant cell tissue and organ culture (1992); 31:161-7.
38. Sheerman S, Bevan M. A rapid transformation method for Solanum tuberosum using binary Agrobacterium tumefaciens vectors. Plant Cell Reports (1998); 7:13-6.
39. Lambe P, Schie H, Mutambel H, Fouche J, Deltour R, Foidart J. DNA methylation as a key process in regulation of organogenic totipotency and plant neoplastic progression? In Vitro Cell Dev Biol (1997); 33:155-62.
40. Turhan H. Callus induction and growth in transgenic potato genotypes. African Journal of Biotechnology (2004); 3(8):375-8.
41. Ryu DD, Lee SO, Romani RJ. Determination of growth rate for plant cell cultures: comparative studies. Biotech Bioeng (1990); 35:305-11.
42. Jiménez V. Involvement of plant hormones and plant growth regulators on in vitro somatic embryogenesis. Plant Growth Regulation (2005); 47:91-110.
43. Rakoczy-Tojanowska M. The effects of growth regulators on somaclonal variation in rye (Secale cereale L.) and selection of somaclonal variants with increased agronomic treats. Cellular & Molecular Biology Letters (2002); 7:1111-20.
44. Hébert-Soulé D, Kikkert J, Reisch B. Phosphinothricin stimulates somatic embryogenesis in grape (Vitis sp. L). Plant Cell Reports (1995); 14:380-4.
45. Toldi O, Tóth S, Oreifig A, González A, Kiss E, Jenes B. Phosphinothricin: a herbicide o ra synthetic cytokinin? Journal of Experimental Botany (Supplement) (1999); 50:56.
46. Toldi O, Tóth S, Oreifig A, Kiss E, Jenes B. Production of phosphinothricin-tolerant rice (Oryza sativa L.) through the application of phosphinothricin as growth regulator. Plant Cell Reports (2000); 19:1226-31.
47. Hoshino Y, Mii M. Bialaphos stimulates shoot regeneration from hairy roots snapdragon (Antirrhinum majus L.) transformed by Agrobacterium rhizogenes. Plant Cell Report (1998); 17:256-61.
48. Wright M, Launis K, Bowman C, Hill M, Dimaio J, Kramer C, et al. A rapid visual method to identify transformed plants. In Vitro Cell Dev Biol-Plant (1996); 32:11-13.