[1] Clive James,Anatole F K.Global review of the field testing and commercialization of transgenic plants 1986to1995[R].The International Service for the Acquisition of Agri-biotech Applications(LSAAA),1996.
[2] Ebinuma H,Sugita K,Matsunaga E,et al.Selection of marker-free transgenicplants using theisopentenyl transferasegene[J].Proc Natl Acad Sci USA,1997,94:2117-2121.
[3] Ebinuma H,Komamine A.MAT(Multi-Auto-Transformation) vector system,the oncogenes of Agrobacterium as positive markets for regeneration and selection of mark-free transgenic plants[J].In Vitro Cell Dev-P1,2001,37:103-113.
[4] Weisser P,Kramer R,Sprenger G A.Expression of the Escherichia coli pmi gene,encoding phosphomannoseisomerase in Zymomonas mobilis,leads to utilization of mannoso as a novel growth substrate,which can be used as a selective marker[J].Appl Environ Miembiol,1996,62(11):4155-4161.
[5] Corneille S,Lutz K,Svab Z,et al.Efficient elimination of selectuble marker genes from the phastid genome by the CRElox Site-specific recombination system[J].Plant J,2001,27(2):171-178.
[6] Reiner G.Genes for ribitol and D-arabitol catabolism in Escherichia coli:their loci in C strains and absence in K-12 and B strains[J].J Bacterial,1975,123:530-536.
[7] 钱方,安利佳,李宪臻.正向选择的生物安全标记基因[J].中国工程生物杂志,2007,27(3):115-119.
[8] Daniell H,Muthukumar B,Lee S B.Marker free transgenic plants:engineering the chloroplast genome without the use of antibiotic selection[J].Curr Genet,2001,39:109-116.
[9] 朱生伟,秦红敏,孙敬三,等.绿色荧光蛋白基因(GFP)在抗虫转基因植物中的应用[J].植物学报,2003,45(6):654-658.
[10] Chung B C,Kim J K,Nahm B H.In plants visual monitoring of green fluorescent protein in transgenic rice plants[J].Mol Cell,2000,10:411-414.
[11] Zhang C L,Chen D F,Mcorma A C,et al.Use of the GFP reporter as a vital marker for Agrobacterium-mediated transformation of sugar beet(Beta vulgaris L.)[J].Mol Biotechnol,2001,17(2):109-117.
[12] Okkels F T,Wars J,Joersbo M.synthesis of cytokinin glucuronides for the selection of transgenic plant cells[J].Phytochem,1997,46:801-804.
[13] Ebinuma H,Sngita K,Matsunaga E,et al.Selection of marker-free transgenieplants using the isopentenyl transferasegene[J].Proc Natl Acad Sci USA,1997,94:2117-2121.
[14] MeKnight T D,Lillis M T,Simpson R B.Segregation of genes transferred to one plant cell from two separate Agrobacterium strains[J].Plant Mol Biol,1987,8:439-445.
[15] De Framond A J,Back E W,Chilon W S,et al.Two unlinked T-DNAs can transform the same tobacco plant cell and segregate in the F1 generation[J].Mol Gen Genet,1986,202:125-131.
[16] Matthews P R,Wang M B,Waterhouse P M,et al.Marker gene elimination from transgenic barley,using transformation with contiguous "twin T-DNAs" on a standard agrobacteriumtransform ation vector[J].Molecular Breeding,2001,7(3):195-202.
[17] Lu H,Zhou X,Gong Z,et al.Generation of selectable marker-free transgenic rice using double right-border(DBR) binary vectors[J].Aust J Plant Physiol,2001,28:241-248.
[18] Fischer N,Stampacchia O,Redding K,et al.Selectable marker recycling in the chloroplast[J].Mol Gen Genet,1996,251(3):373.
[19] De Block M,Debrouwer D.Two T-DNAs co-transformed into Brassica napus by a double Agrobacterium tumefaciens infection are mainly integrated at the same locus[J].Theor Appl Genet,1991,82:257-263.
[20] Zubko E,Scutt C,Meyer P.Intrachromosomal recombination between attp regions as a tool to remove selectable marker genes from tobacco transgenes[J].Nat Biotechnology,2000,18:442-445.
[21] Sugita K,Matsunaga E,Ebinuma H.Effective selection system for generating marker-free transgenic plants independent of sexual crossing[J].Plant Cell Report,1999,18:941-947.
[22] Sugita K,Kasahara T,Matsunaga E,el al.A transformation vector for the production of marker-free transgenic plants containing a single copy transgene at high frenquency[J].Plant Journal,2000,22:461-469.
[23] Barry G F.Indentifiction of a cloned cytokinin biosynthetic gene[J].Proc Natl Acad Sci USA,1984,81:4776-4780.
[24] Cregg J M,Madden K R.Use of site-specific recombination to regenerate selectable markers[J].Mol Gen Genet,1989,219:320-323.
[25] Lyznik L,Mitchell J C,Hirayama L.Activity of yeast FIP recombinase in maize and rice protoplasts[J].Nucl Acids Res,1993,214:969-975.
[26] Onouchi H,Nishihama R,Kuodo M,et al.Visualization of site-specific recombination catalyzed by a recombinase of Zygosaccharomyces rouxii Arabdopsis thaliana[J].Mol Gen Gent,1995,247:653.
[27] Maeser S,Kahmann R.The Gin recombinase of phage Mu can catalyse site-specific recombination in plant protoplasts[J].Mol Gen Genet,1991,230:170-176.
[28] Fedoroff N.Maize transposable elements[J].American Society for Microbiology,1989:375-411.
[29] Goldsbrough A P,Lastrella C N,Yoder J I.Transposition mediated re-positioning and subsequent elimination of marker genes from transgenic tomato[J].Biotechnology,1993,11:1286-1292.
[30] Iamtham S,Day A.Removal of antibiotic resistance genes from transgenic tobacco plastids[J].Nat Biotechnol,2000,18(11):1172-1176.
[31] Hajdukiewicz P T,Gilbertson L,Staub J M.Multiple pathways for Cre/lox-mediated recombination in plastids[J].Plant J,2001,27(2):161-170.
[32] Lutz K A,Bosacchi M H,Maliga P.Plastid marker-gene excision by transiently expressed CRE recombinase[J].Plant J,2006,45(3):447-456.
[33] Zuo J,Niu Q W,Moller S G,et al.Chemical-regulated sitespcific DNA excision in transgenic plants[J].Nat Biotechnol,2001,19(2):115-116. |