Abstract
Chicory, a member of the Asteraceae family, is a dioecious species (2x = 2n = 18). In Europe three species are usually grown. Cichorium endivia L. and C. spinosum L. are annuals predominantly grown in southern Europe and northern Africa and consumed as salads, whereas C. intybus L. comprises annual, biennial or perennial varieties which are widespread in Europe and Asia, and have been naturalised in America, Australia and South Africa. For a long time, C. intybus was used as a medicine, or as a foodstuff by humans and cattle. Besides endive and curly endive, some other varieties with large and more or less red leaves are predominantly grown in Italy (cv. Verona, Trevisia, Chioggia), and consumed as salads as well. The varieties sativum (= Magdeburg) and Witloof are usually grown as biennials and are mainly cultivated in the Netherlands, Belgium and North of France.
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References
Abid M, Palms B, Derycke R, Tissier JP, Rambour S (1995) Transformation of chicory and expression of the bacterial uidA and nptII genes in the transgenic regenerants. J Exp Bot 46:337–346
Assad-Garcia N, Ochoa-Alejo N, Garcia-Hernandez E, Herrera-Estrella L, Simpson J (1992) Agrobacterium-mediated transformation of tomatillo (Physalis ixocarpa) and tissue specific and developmental expression of the CaMV 35S promoter in transgenic tomatillo plants. Plant Cell Rep 11:558–562
Benfey PN, Chua N-H (1989) Regulated genes in transgenic plants. Science 244:174–181
Benfey PN, Ren L, Chua N-H (1990a) Tissue-specific expression from CaMV 35S enhancer subdomains in early stages of plant development. EMBO J 9:1677–1684
Benfey PN, Ren L, Chua N-H (1990b) Combinatorial and synergistic properties of CaMV 35S enhancer subdomains. EMBO J 9:1685–1696
Bradford MM (1976) A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Ann Biochem 72:248–254
Deblaere R, Byteber B, De Greve H, Deboeck F, Schell J, Van Montagu M, Leemans J (1985) Efficient atropine Ti-plasmid derived vectors for Agrobacterium-mediated gene transfer to plants. Nucleic Acids Res 13:4777–4788
Dellaporta SL, Wood J, Hicks JB (1983) A plant DNA minipreparation; version II. Plant Mol Biol Rep 1:19–21
Dong J-Z, Yang M-Z, Jia S-R, Chua N-H (1991) Transformation of melon (Cucumis melo L.) and expression from the Cauliflower Mosaic Virus 35S promoter in transgenic melon plants. Biotechnology 9:858–863
Ebert PR, Ha SB, An G (1987) Identification of an essential upstream element in the nopaline synthase promoter by stable and transient assays. Proc Natl Acad Sci USA 84:5745–5749
Feltkamp D, Baumann E, Schmalenbach W, Masterson R, Rosahl S (1995) Expression of the mannopine synthase promoter in roots is dependent on the mas elements and correlates with high transcript levels of mas-binding factor. Plant Sci 109:57–65
Fiala V, Jolivet E (1984) Mise en évidence d’une nouvelle fraction glucidique dans la racine de chicorée et son évolution au cours de la formation des réserves. Physiol Vég 22:315–321
Foley RC, Grossmann C, Ellis JG, Llewellyn DJ, Dennis ES (1993) Isolation of a maize bZIP protein subfamily:candidates for the ocs-element transcription factor. Plant J 3:669–679
Frulleux F, Weyens G, Jacobs M (1997) Agrobacterium tumefaciens-mediated transformation of shoot-buds of chicory. Plant Cell, Tissue and Organ Culture, 50:107–112
Gautheret RJ (1941) Recherches expérimentales sur la polarite des tissus de la racine d’Endive. C R Acad Sci SerIII-Vie 213:37–39
Genga A, Giansante L, Bernacchia G, Allavena A (1994) Plant regeneration from Cichorium intybus L. leaf explants transformed by Agrobacterium tumefaciens. J Genet Breed 48:25–32
Guevara-Garcia A, Mosqueda-Cano G, Argiielio-Astorga G, Simpson J, Herrera-Estrella L (1993) Tissue-specific and wound-inducible pattern of expression of the mannopine synthase promoter is determined by the interaction between positive and negative cis-regulatory elements. Plant J 4:495–505
Heller R (1953) Recherche sur la nutrition minérale des tissus végétaux cultivés in vitro. Ann Sci Nat Bot 14:1–223
Jefferson RA, Kavanagh TA, Bevan MW (1987) GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6:3901–3907
Lam E, Benfey PN, Gilmartin PM, Fang R-X, Chua N-H (1989) Site-specific mutations alter in vitro factor binding and change promoter expression pattern in transgenic plants. Proc Natl Acad Sci USA 86:7890–7894
Langridge WHR, Fitzgerald KJ, Koncz C, Schell J, Szalay AA (1989) Dual promoter of Agrobacterium tumefaciens mannopine synthase genes is regulated by plant growth hormones. Proc Natl Acad Sci USA 86:3219–3223
Leung J, Fukuda H, Wing D, Schell J, Masterson R (1991) Functional analysis of cis-elements, auxin response and early developmental profiles of the mannopine synthase bidirectional promoter. Mol Gen Genet 230:463–474
Lu C-Y, Nugent G, Wardley-Richardson T, Chandler SF, Young R, Dalling MJ (1991) Agrobacterium-mediated transformation of carnation (Dianthus caryophyllus L.) Bio/Technology 9:864–868
Mascarenhas JP, Hamilton DA (1992) Artifacts in the localization of GUS activity in anthers of petunia transformed with a CaMV 35S-GUS construct. Plant J 2:405–408
McCormick S, Twell D, Wing R, Ursin V, Yamaguchi J, Larabell S (1989) Anther-specific genes: molecular characterization and promoter analysis in transgenic plants. In: Lord E, Bernier G (eds) Plant reproduction: from floral induction to pollination. Am Soc Plant Physiol, Rockville, MD, pp 128–135
McCowan PP, Chen KJ, Barley CMB, Costerton JW (1978) Adhesion of bacteria to epithelial cell surfaces of the reticulo-rumen of cattle. Appl Environ Microbiol 35:149–155
Mendel RR, Muller B, Schulze Y, Kolesnikov V, Zelenin A (1989) Delivery of foreign genes to intact barley cells by high velocity microprojectiles. Theor Appl Genet 78:31–34
Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–497
Ni M, Cui D, Gelvin SB (1994) Wound inducibility and tissue specificity of chimaeric promoters derived from the mannopine and octopine synthase genes. 4th Int Congr Plant Mol Biol, 19–24 June 1994, Amsterdam
Pena-Cortes H, Sanchez-Serano JJ, Mertens R, Willmitzer L (1989) Abscisic acid is involved in the wound-induced expression of the proteinase inhibitor II gene in potato and tomato. Proc Natl Acad Sci USA 86:9851–9855
Pena-Cortes H, Fisahn J, Willmitzer L (1995) Signals involved in the wound-induced proteinase inhibitor II gene expression in tomato and potato plants. Proc Natl Acad Sci USA 92:4106–4113
Rubery PH (1987) Auxin transport. In: Davies PJ (ed) Plant hormones and their role in plant growth and development. Martinus Nijhoff, The Hague, pp 341–362
Saito K, Yamazaki M, Kaneko H, Murakoshi I, Fukuda Y, Van Montagu M (1991) Tissue-specific and stress-enhancing expression of the TR promoter for mannopine synthase in transgenic medicinal plants. Planta 184:40–46
Sambrook J, Fritsh EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York
Schneider M, Ow DW, Howell SH (1990) The in vivo pattern of firefly luciferase expression in transgenic plants. Plant Mol Biol 14:935–947
Stefanov I, Fekete S, Bögre L, Pauk J, Feher A, Dudits D (1994) Differential activity of the mannopine synthase and the CaMV 35S promoters during development of transgenic rapeseed plants. Plant Sci 95:175–186
Sun LY, Touraud G, Charbonnier C, Tepfer D (1991) Modification of phenotype in Belgian endive (Cichorium intybus) through genetic transformation by Agrobacterium rhizogenes: conversion from biennial to annual flowering. Transg Res 1:14–22
Teeri TH, Lehvaslaiho H, Franck M, Uotila J, Heino P, Paiva ET, Van Montagu M, Herrera-Estrella L (1989) Gene fusions to lacZ reveal new expression patterns of chimeric genes in transgenic plants. EMBO J 8:343–350
Terada R, Shimamoto K (1990) Expression of CaMV-GUS gene in transgenic rice plants. Mol Gen Genet 220:389–392
Twell D, Yamaguchi J, Wing RA, Ushiba J, Mc Cormick S (1991) Promoter analysis of three genes that are coordinately expressed during pollen development reveals pollen-specific enhancer sequences and shared regulatory elements. Gene Dev 5:496–507
Vallès MP, Lasa JM (1994) Agrobacterium-mediated transformation of commercial melon (Cucumis melo L., cv. Amarillo Oro). Plant Cell Rep 13:145–148
Vermeulen A, Vaucheret H, Pautot V, Chupeau Y (1992) Agrobacterium-mediated transfer of a mutant Arabidopsis acetolactate synthase gene confers resistance to chlorsulfuron in chicory (Cichorium inthybus L.). Plant Cell Rep 11:243–247
Vijn I, Van Dijken A, Sprenger N, Van Dun K, Weisbeek P, Wiemken A, Smeekens S (1997) Fructan of the inulin neoseries is synthesized in transgenic chicory plants (Cichorium intybus L.) harbouring onion (Allium cepa L.) fructan:fructan 6G fructosyltransferase. Plant J 11:387–398
Wagner VT, Cresti M, Salvatici P, Tiezzi A (1990) Changes in volume, surface area, and frequency of nuclear pores on the vegetative nucleus of tobacco pollen in fresh hydrated and activated conditions. Planta 181:304–309
Williamson JD, Hirsch-Wyncott ME, Lankins BA, Gelvin SB (1989) Differential accumulation of a transcript driven by the CaMV 35S promoter in transgenic tobacco. Plant Physiol 90:1570–1576
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Abid, M., Huss, B., Rambour, S. (2001). Transgenic Chicory (Cichorium intybus L.). In: Bajaj, Y.P.S. (eds) Transgenic Crops II. Biotechnology in Agriculture and Forestry, vol 47. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56901-2_8
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DOI: https://doi.org/10.1007/978-3-642-56901-2_8
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