Use of Chenopodium murale L. transgenic hairy root in vitro culture system as a new tool for allelopathic assays

Journal of Plant Physiology

Volumn 169, Issue 12, 2012, Pages 1203-1211

  Mitić, Nevena ^a   Dmitrović, Slavica ^a   Djordjević, Mirka ^a   Zdravković Korać, Snežana ^a   Nikolić, Radomirka ^a   Raspor, Martin ^a   Djordjević, Tatjana ^a   Maksimović, Vuk ^b   Živković, Suzana ^a   Krstić Milošević, Dijana ^a   Stanišić, Mariana ^a   Ninković, Slavica ^a  

^a UNIVERSITY OF BELGRADE   (Serbia)

^b UNIVERSITY OF BELGRADE   (Serbia)

Author keywords

Agrobacterium rhizogenes; Allelopathy; Chenopodium murale; Genetic transformation; Hairy roots; Phenolic acids; Rol genes

Indexed keywords

PHEROMONE;

ARTICLE; CELL CLONE; CHEMISTRY; CHENOPODIUM; COMPARATIVE STUDY; COTYLEDON; CULTURE MEDIUM; CULTURE TECHNIQUE; CYTOLOGY; GENE EXPRESSION REGULATION; GENETIC TRANSFORMATION; GENETIC VARIABILITY; GENETICS; GROWTH, DEVELOPMENT AND AGING; METHODOLOGY; MICROBIOLOGY; PLANT LEAF; PLANT ROOT; RHIZOBIUM; SEEDLING; TRANSGENIC PLANT;

AGROBACTERIUM; CHENOPODIUM; CLONE CELLS; COTYLEDON; CULTURE MEDIA; CULTURE TECHNIQUES; GENE EXPRESSION REGULATION, PLANT; GENETIC VARIATION; PHEROMONES; PLANT LEAVES; PLANT ROOTS; PLANTS, GENETICALLY MODIFIED; SEEDLING; TRANSFORMATION, GENETIC;

AGROBACTERIUM RHIZOGENES; CHENOPODIUM; CHENOPODIUM MURALE; LACTUCA; TRITICUM AESTIVUM;

EID: 84863880682     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2012.04.009     Document Type: Article

References (42)

1. Alpizar E., Dechamp E., Espeout S., Lecouls A.C., Nicole M., Bertrand B., et al. Efficient production of Agrobacterium rhizogenes-transformed roots and composite plants for studying gene expression in coffee roots. Plant Cell Rep 2006, 25:959-967.
2. Alpizar E., Dechamp E., Lapeyre-Montes F., Guilhaumon C., Bertrand B., Jourdan C., et al. Agrobacterium rhizogenes-transformed roots of coffee (Coffea arabica): conditions for long-term proliferation, and morphological and molecular characterization. Ann Bot 2008, 101:929-940.
3. Batish D.R., Lavanya K., Pal Singh H., Kohli R.K. Root-mediated allelopathic interference of nettle-leaved goosefoot (Chenopodium murale) on wheat (Triticum aestivum). J Agron Crop Sci 2007, 193:37-44.
4. Batish D.R., Lavanya K., Pal Singh H., Kohli R.K. Phenolic allelochemicals released by Chenopodiummurale affect the growth, nodulation and macromolecule content in chickpea and pea. Plant Growth Regul 2007, 51:119-128.
5. Chaudhuri K.N., Ghosh B., Tepfer D., Jha S. Genetic transformation of Tylophora indica with Agrobacterium rhizogens A4: growth and tylophorine productivity in different transformed root clones. Plant Cell Rep 2005, 24:25-35.
6. Cumming B.G. Early flowering plants. Methods in developmental biology 1967, 277-299. Cromwell TY, New York. F.H. Will, N.K. Wesselss (Eds.).
7. Datta S.C., Ghosh K.N. Allelopathy in two species of Chenopodium, inhibition of germination and seedling growth of certain weeds. Acta Soc Bot Pol 1987, 56:257-270.
8. Dmitrović S., Mitić N., Zdravković-Korać S., Vinterhalter B., Ninković S., ćulafić Lj. Hairy roots formation in recalcitrant-to-transform plant Chenopodium rubrum. Biol Plant 2010, 54:566-570.
9. El-Khatib A.A., Hegazy A.K., Galal H.K. Allelopathy in the rhizosphere and amended soil of Chenopodium murale L. Weed Biol Manage 2004, 4:35-42.
10. El-Khatib A.A., Hegazy A.K., Galal H.K. Does allelopathy have a role in the ecology of Chenopodiummurale?. Ann Bot Fennici 2004, 41:37-45.
11. Flores Solís J.I., Mlejnek K., Studená S., Procházka S. Application of sonication-assisted Agrobacterium-mediated transformation in Chenopodium rubrum L. Plant Soil Environ 2003, 49:255-260.
12. Gašić K., Hernandez A., Korban S.S. RNA extraction from different apple tissues rich in polyphenols and polysaccharides for cDNA library construction. Plant Mol Biol Rep 2004, 22:437a-1437a.
13. Gelvin S.B. Agrobacterium and plant genes involved in T-DNA transfer and integration. Annu Rev Plant Physiol Plant Mol Biol 2000, 51:223-256.
14. Golisz A., Sugano M., Fujii Y. Microarray expression profiling of Arabidopsis thaliana L. in response to allelochemicals identified in buckwheat. J Exp Bot 2008, 59:3099-3109.
15. Golisz A., Sugano M., Hiradate S., Fujii Y. Microarray analysis of Arabidopsis plants in response to allelochemical l-DOPA. Planta 2011, 233:231-240.
16. Gonçalves S., Ferraz M., Romano A. Phytotoxic properties of Drosophyllum lusitanicum leaf extracts and its main compound plumbagin. Sci Hortic 2009, 122:96-101.
17. Holm L., Doll J., Holm E., Pancho J., Herberger J. World weeds: natural histories and distribution 1997, New York, John Wiley & Sons Inc.
18. Jefferson R.A., Kavanagh T.A., Bevan M.W. GUS fusions: β-glucuronidase as a sensitive and versatilegene fusion marker in higher plants. EMBO J 1987, 6:3901-3907.
19. Jung J.-L., Bouzoubaa S., Gilmer D., Hahne G. Visualization of transgene expression at the single protoplast level. Plant Cell Rep 1992, 11:346-350.
20. Kang H.J., Anbazhagan V.R., You X.L., Moon H.K., Yi J.S., Choi Y.E. Production of transgenic Aralia elata regenerated from Agrobacterium rhizogenes-mediated transformed roots. Plant Cell Tissue Organ Cult 2006, 85:187-196.
21. Kato-Noguchi H., Ino T. Possible involvement of momilactone B in rice allelopathy. J Plant Physiol 2005, 162:718-721.
22. Kato-Noguchi H. Allelochemicals released from rice plants. Jpn J Plant Sci 2008, 2:18-25.
23. Kato-Noguchi H., Hasegawa M., Ino T., Ota K., Kujime H. Contribution of momilactone A and B to rice allelopathy. J Plant Physiol 2010, 167:787-791.
24. Komari T. Transformation of cultured cells of Chenopodium quinoa by binary vectors that carry a fragment of DNA from the virulence region of pTiBo542. Plant Cell Rep 1990, 9:303-306.
25. Mallol A., Cusidó R.M., Palazón J., Bonfill M., Morales C., Piñol M.T. Ginsenoside production in different phenotypes of Panax ginseng transformed roots. Phytochemistry 2001, 57:365-371.
26. Milivojević S., Mitrović A., ćulafić Lj. Somatic embryogenesis in Chenopodium rubrum and Chenopodium murale in vitro. Biol Plant 2005, 49:35-39.
27. Mirjalili H.M., Fakhr-Tabatabaei S.M., Bonfill M., Alizadeh H., Cusidó R.M., Ghassempour A., et al. Morphology and withanolide production of Withania coagulans hairy root cultures. Eng Life Sci 2009, 9:197-204.
28. Moyano E., Fornalé J., Palazón J., Cusidó R.M., Bonfill M., Morales C., et al. Effect of Agrobacterium rhizogenes T-DNA on alkaloid production in Solanaceae plants. Phytochemistry 1999, 52:1287-1292.
29. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 1962, 15:473-497.
30. Murray M.G., Thompson W.F. Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res 1980, 8:4321-4325.
31. Porwal M.K., Gupta O.P. Allelopathic influence of winter weeds on germination and growth of wheat. Int J Trop Agric 1986, 4:276-279.
32. Qasem J.R. Aqueous extracts of nettle-leaved goosefoot (Chenopodium murale L.) on wheat and barley. Res J Aleppo Univ (Agric Sci Ser) 1990, 14:37-53.
33. Qasem J.R. Allelopathic effect of Amaranthus retroflexus and Chenopodium murale on vegetable crops. Allelopathy J 1995, 2:49-66.
34. Schmidt J.F., Moore M.D., Pelcher L.E., Covello P.S. High efficiency Agrobacterium rhizogenes-mediated transformation of Saponaria vaccaria L. (Caryophyllaceae) using fluorescence selection. Plant Cell Rep 2007, 26:1547-1554.
35. Soltys D., Rudzińska-Langwald A., Kurek W., Gniazdowska A., Sliwinska E., Bogatek R. Cyanamide mode of action during inhibition of onion (Allium cepa L.) root growth involves disturbances in cell division and cytoskeleton formation. Planta 2011, 234:609-621.
36. Taneja J., Jaggi M., Wankhede D.P., Sinha A.K. Effect of loss T-DNA genes on MIA biosynthetic pathway gene regulation and alkaloid accumulation in Catharanthus roseus hairy roots. Plant Cell Rep 2010, 29:1119-1129.
37. Tepfer M., Casse-Delbart F. Agrobacterium rhizogenes as a vector for transforming higher plants. Microbiol Sci 1987, 4:24-28.
38. Tiwari R.K., Trivedi M., Guang Z.-C., Guo G.-Q., Zheng G.-C. Genetic transformation of Gentianamacrophylla with Agrobacterium rhizogenes: growth and production of secoiridoid glucoside gentiopicrosid in transformed hairy root cultures. Plant Cell Rep 2007, 26:199-210.
39. Triplett B.A., Moss S.C., Bland J.M., Dowd M.K. Induction of hairy root cultures from Gossypiumhirsutum and Gossypium barbadense to produce gossypol and related compounds. In Vitro Cell Dev Biol Plant 2008, 44:508-517.
40. Vervliet G., Holsters M., Teuchy H., Van Montagu M., Schell J. Characterization of different plaque forming and defective temperate phages in Agrobacterium. J Gen Virol 1975, 26:33-48.
41. Wubben M.J., Callahan F.E., Triplett B.A., Jenkins J.N. Phenotypic and molecular evaluation of cotton hairy roots as a model system for studying nematode resistance. Plant Cell Rep 2009, 28:1399-1409.
42. Zhang Y., Gu M., Shi K., Zhou Y.H., Yu J.Q. Effects of aqueous root extracts and hydrophobic root exudates of cucumber (Cucumis sativus L.) on nuclei DNA content and expression of cell cycle-related genes in cucumber radicles. Plant Soil 2010, 327:455-463.