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Factors Affecting the Level of Kanamycin Resistance in Transformed Sunflower Cells
Author(s) -
Robert C. Nutter,
Nicholas P. Everett,
Dorothy A. Pierce,
Lucy Panganiban,
Patricia A. Okubara,
Rosanna Lachmansingh,
Desmond Mascarenhas,
Heather Welch,
Irvin J. Mettler,
Lucille Pomeroy,
Jill L. Johnson,
John A. Howard
Publication year - 1987
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.84.4.1185
Subject(s) - plasmid , biology , microbiology and biotechnology , octopine , kanamycin , gene , xhoi , selectable marker , expression cassette , ti plasmid , genetics , agrobacterium tumefaciens , transformation (genetics) , vector (molecular biology) , recombinant dna , ecori
A 230 base pair DNA segment containing the sequences 5' to the 700 to 750 nucleotide (nt) transcript 7' (ORF 3; RF Barker, KB Idler, DV Thompson, JD Kemp 1983 Plant Mol Biol 2: 335-350) of the octopine tumor inducing plasmid pTiA6 has been isolated. This region has (a) 180 base pairs of DNA upstream of the TATA box, (b) the start of RNA synthesis, and (c) the entire 5' untranslated region of the gene. We have fused this presumed promoter fragment to the neomycin phosphotransferase II (NPTII) gene from Tn5 in a plant expression cassette. After recombination into a tumor inducing plasmid delivery plasmid, this cassette confers selectable kanamycin resistance to transformed sunflower cells. Removal of the out-of-frame ATG in the 5' leader sequence of the NPTII gene by two different modifications increased both the levels of NPTII enzyme activity and the ID(50) for kanamycin in the tumor cells. The promoter region of the transcript 7 gene gives levels of kanamycin resistance equivalent to the nopaline synthase promoter and octopine synthase promoter when used in the same constructions and assayed in the same tissues.

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