Improved expression of streptomycin resistance in plants due to a deletion in the streptomycin phosphotransferase coding sequence View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1988-11

AUTHORS

Pal Maliga, Zora Svab, Elisabeth C. Harper, Jonathan D. G. Jones

ABSTRACT

Previous studies have shown that a chimeric streptomycin phosphotransferase (SPT) gene can function as a dominant marker for plant cell transformation. The SPT marker previously described by Jones and co-workers has a limited value since it conferred a useful level of resistance only to a fraction (10%) of Nicotiana plumbaginifolia transgenic lines. Expression of resistance was species specific: no such resistant transformants were found in N. tabacum. In this paper we describe an improved SPT construct that utilizes a mutant Tn5 SPT gene. The mutant gene, SPT*, encodes a protein with a two amino acid deletion close to its COOH-terminus. In N. tabacum cell culture the efficiency of transformation with the improved streptomycin resistance marker was comparable to kanamycin resistance. When the chimeric SPT* gene was introduced linked to a kanamycin resistance gene, streptomycin resistance was expressed in most of the transgenic N. tabacum lines. More... »

PAGES

456-459

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00330480

DOI

http://dx.doi.org/10.1007/bf00330480

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016718391

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2851095


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