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Study on Agrobacterium-mediated Transformation of Vitis vinifera (L.) and Plant Regeneration(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2012年19期
Page:
113-117
Research Field:
Publishing date:

Info

Title:
Study on Agrobacterium-mediated Transformation of Vitis vinifera (L.) and Plant Regeneration
Author(s):
TAN ChaoZHANG Jian-xiaWANG Yue-jin
Key Laboratory of Melecular Biology of Shaanxi Province,Key Opening Laboratory of Plant Germplasm Resources,Northwest Gardening Plants of Ministry of Agricultural,College of Horticulture,Northwest Agricultural and Forestry University,Yangling,Shaanxi 712100
Keywords:
Vitis viniferafloral organsomatic embryoplant regenerationgenetic transformation
PACS:
S 663.103.6
DOI:
-
Abstract:
Stamen,pistils and flower buds from Vitis vinifera cvs.‘Thompson Seedless’,‘Carignane’ and ‘Red Globe’ were used as explants to investigate their efficience of embryonic callus induction and Agrobacterium-mediated stilbene synthase gene transformation.The results indicated that MC medium was optimum for embryonic callus induction from stamens among 5 medium for embryonic callus induction.The induction rate in ‘Thompson Seedless’,‘Carignane’ and ‘Red Globe’ were 1.7% 0.3% and 11.8%,respectively.Embryonic callus from ‘Thompson Seedless’ and ‘Carignane’ could be induced in PIV medium with 4.0% and 3.2% induction rates.However,the highest induction rate occurred in embryonic callus from flower buds of ‘Red Globe’ in MC medium with 5.6% induction rate.Only flower buds from Redglobe could be induced in MS1 medium with 0.5% induction rate.A modified X6 liquid medium was suitable for secondary embryogenesis,and medium B favored germination and seedling of somatic embryos.Transformed plants were selected through resistance screening and 2 resistent plants of ‘Thompson Seedless’ were obtained.Results from PCR and PCR-Southern indicated that stilbene synthase gene were integrated into the genome of ‘Thompson Seedless’.

References:

[1]曲泽洲,孙云蔚.果树种类论[M].北京:中国农业出版社,1990:113-114.

[2]华南农业大学.果树栽培学各论[M].北京:中国农业出版社,1981:404-406.

[3]Jayasankar SGray D JLitz R E.High-efficiency somatic embryogenesis and plant regeneration from suspension cultures of grapevine[J].Plant Cell Reports,1999(18):533-537.

[4]Gresshoff P M,Doy C H.Derivation of a haploid cell line from Vitis vinfiera and the importance of the stage of meiotic development of anthers for haploid culture of this and other genera[J].Z Pflanzenphysiol,1974,73:123-141.

[5]Srinivasan CMullins M G.High-frequency somatic embryo production from unfertilized ovules of grapes[J].Scientia Horticulturae1980(13):245-252.

[6]Dhekney S ALi Z T.Optimizing Initiation and Maintenance of Vitis?Embryogenic Cultures[J].Hort Science,2009,445:1400-1406.

[7]Das D KReddy M KUpadhyaya K Cet al.An efficient leaf disc culture method for the regeneration via somatic embryogenesis and transformation of grape(Vitis vinifera L.)[J].Plant Cell Rep,2002(20):999-1005.

[8]Popesc C F.Somatic embryogenesis and plant development from anther culture of Vitis vinifera?L[J].Plant Growth Reg,1996,20:75-78.

[9]Perl A,Saad S,Sahar N,et al.Establishment of long-term embryogenic cultures of seedless Vitis vinifera?cultivars-a synergistic effect of auxins and the role of abscisic acid[J].Plant Science,1995,104:193-200.

[10]Gambino GRuffa PVallania Ret al.Somatic embryogenesis from whole flowersanthers and ovaries of grapevine(Vitis?spp.)[J].Plant Cell Tiss Organ Cult,2007,90:79-83.

[11]Mauro M CToutain SWalter Bet al.High efficiency regeneration of grapevine plants transformed with the GFLV coat protein gene[J].PlantScience,1995,112:97-106.

[12]Gray D JMeredith CGrape P.Biotechonoloyg of perennial fruit crops[D].Wallingford:Hammersch lag FA,Litz RE,eds.CAB Intemational1992:229-262.

[13]Salunkhe C K,Raopsmha T.Induction of somatic embryogenesis and plantlets intendrils of?Vitis vinifera?L[J].Plant Cell Rep,1997,17:65-70.

[14]Kikkert J RStriem M JVidal J Ret al.Long-term study of somatic embryogenesis from anthers and ovaries of 12 grapevine (Vitis?sp.)genotypes[J].In Vitro Cellular & Developmental Biology Plant,2005,41:232-239.

[15]Li Z TDhekney S ADutt Met al.Optimizing Agrobacterium-mediated transformation of grapevine[J].In Vitro Cellular & Developmental Biology Plant,2006,42(3):220-227.

[16]Kasajima IIde YOhkama-Ohtsu Net al.A protocol for rapid DNA extraction from Arabidopsis thaliana for PCR analysis[J].Plant Mol Biol Rep,2004(22):49-52.

[17]Dhekney S ALi Z TGray D J.Factors induencing induction and maintenance of Vitis rotundifolia?Michx.Embryogenic cultures[J].Plant Cell Tiss Organ Cult,2011,105:175-180.

[18]Raemakers C J J MJacobsen EVisser R G F.Secondary somatic embryogenesis and applications in plant breeding[J].Euphytica,1995,81:93-107.

[19]肖宇,张朝红,支玉玺,.葡萄花器官体细胞胚的诱导和植株再生[J].果树学报,2011,28(5):888-892.

[20]Bao YLiu G FShi X Pet al.Primary and repetitive secondary somatic embryogenesis in Rosa hybrida Samantha[J].Plant Cell Tissue and Organ Culture,2012(1):1-8.

[21]Martinelli LCandioli ECosta Det al.Morphogenic competence of Vitis rupestris S.secondary somatic embryos with a long culture history[J].Plant Cell Rep,2001(20):279-284.

[22]López-Pérez A JCarreňo JMartínez-Cutillas A.High embryogenic ability and plant regeneration of table grapevine cultivars (Vitis vinifera?L.) induced by activated charcoal[J].Vitis,2005,44(2):79-85.

[23]Gray D J,Mortensen J A.Initiation and maintenance of long term somatic embryogenesis from anthers and ovaries of?Vitis longii”Microsperma”[J].Plant Cell Tissue and Organ Culture,1987(9):73-80.

[24]Faure ODewitte WNougaréde A.Precociously germinating somatic embryos of Vitis vinifera?have lower ABA and IAA levels than their germinating zygotic counterparts[J].Physiol Plant,1998,102:591-595.

[25]Dhekney S ALi Z TZimmerman T W.Factors Influencing Genetic Transformation and Plant Regeneration of Vitis[J].Am J Enol Vitic2009,60(3):285-292.

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Last Update: 2014-09-09