Agrobacterium tumefaciens-mediated transformation of poinsettia, Euphorbia pulcherrima, with virus-derived hairpin RNA constructs confers resistance to Poinsettia mosaic virus

被引:35
作者
Clarke, Jihong Liu [1 ]
Spetz, Carl [1 ]
Haugslien, Sissel [1 ]
Xing, Shaochen [1 ,2 ]
Dees, Merete W. [1 ,3 ]
Moe, Roar [3 ]
Blystad, Dag-Ragnar [1 ]
机构
[1] Norwegian Inst Agr & Environm Res, Plant Hlth & Plant Protect Div, N-1432 As, Norway
[2] Jilin Acad Agr Sci, Biotechnol Res Ctr, Changchun 130124, Peoples R China
[3] Norwegian Univ Life Sci, Dept Plant & Environm Sci, N-1432 As, Norway
关键词
Euphorbia pulcherrima; somatic embryogenesis; transformation; Agrobacterium tumefaciens; Poinsettia mosaic virus;
D O I
10.1007/s00299-008-0526-9
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Agrobacterium-mediated transformation for poinsettia (Euphorbia pulcherrima Willd. Ex Klotzsch) is reported here for the first time. Internode stem explants of poinsettia cv. Millenium were transformed by Agrobacterium tumefaciens, strain LBA 4404, harbouring virus-derived hairpin (hp) RNA gene constructs to induce RNA silencing-mediated resistance to Poinsettia mosaic virus (PnMV). Prior to transformation, an efficient somatic embryogenesis system was developed for poinsettia cv. Millenium in which about 75% of the explants produced somatic embryos. In 5 experiments utilizing 868 explants, 18 independent transgenic lines were generated. An average transformation frequency of 2.1% (range 1.2-3.5%) was revealed. Stable integration of transgenes into the poinsettia nuclear genome was confirmed by PCR and Southern blot analysis. Both single- and multiple-copy transgene integration into the poinsettia genome were found among transformants. Transgenic poinsettia plants showing resistance to mechanical inoculation of PnMV were detected by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). Northern blot analysis of low molecular weight RNA revealed that transgene-derived small interfering (si) RNA molecules were detected among the poinsettia transformants prior to inoculation. The Agrobacterium-mediated transformation methodology developed in the current study should facilitate improvement of this ornamental plant with enhanced disease resistance, quality improvement and desirable colour alteration. Because poinsettia is a non-food, non-feed plant and is not propagated through sexual reproduction, this is likely to be more acceptable even in areas where genetically modified crops are currently not cultivated.
引用
收藏
页码:1027 / 1038
页数:12
相关论文
共 71 条
[1]   A large-scale study of rice plants transformed with different T-DNAs provides new insights into locus composition and T-DNA linkage configurations [J].
Afolabi, AS ;
Worland, B ;
Snape, JW ;
Vain, P .
THEORETICAL AND APPLIED GENETICS, 2004, 109 (04) :815-826
[2]   Agrobacterium tumefaciens-mediated transformation of Cyclamen persicum Mill. [J].
Aida, R ;
Hirose, Y ;
Kishimoto, S ;
Shibata, M .
PLANT SCIENCE, 1999, 148 (01) :1-7
[3]  
[Anonymous], 1989, Molecular Cloning
[4]  
[Anonymous], FLOWERTECH
[5]   T-DNA transfer, integration, expression and inheritance in rice:: effects of plant genotype and Agrobacterium super-virulence [J].
Azhakanandam, K ;
McCabe, MS ;
Power, JB ;
Lowe, KC ;
Cocking, EC ;
Davey, MR .
JOURNAL OF PLANT PHYSIOLOGY, 2000, 157 (04) :429-439
[6]   Transformation of Nicotiana benthamiana with the potato mop-top virus coat protein gene produces a novel resistance phenotype mediated by the coat protein [J].
Barker, H ;
Reavy, B ;
McGeachy, KD ;
Dawson, S .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1998, 11 (07) :626-633
[7]   RNA silencing [J].
Baulcombe, D .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (06) :290-293
[8]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[9]  
BLYSTAD DR, 2002, ACTA HORTIC, V568, P225
[10]   Sequence analysis and genome organisation of poinsettia mosaic virus (PnMV) reveal closer relationship to marafiviruses than to tymoviruses [J].
Bradel, BG ;
Preil, W ;
Jeske, H .
VIROLOGY, 2000, 271 (02) :289-297