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Cloning of a yeast dihydrofolate reductase gene inEscherichia coli

✍ Scribed by Kamalendu Nath; Edward W. Baptist


Publisher
Springer-Verlag
Year
1984
Tongue
English
Weight
546 KB
Volume
8
Category
Article
ISSN
0172-8083

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✦ Synopsis


The dihydrofolate reductase gene of Saccharornyces cerevisiae has been isolated by selection of trimethoprim resistant Escherichia coli transformed with a gene bank of yeast DNA in plasmid pBR322. From a 9.2 kilobase pair BamHI DNA fragment this gene has been localized to a 1.76 kb fragment, the restriction map of which appears different from those reported for the E. coli and the mouse dihydrofolate reductase genes.

The enzyme encoded by the chimeric plasmid was established as yeast dihydrofolate reductase by its sensitivity to antifolates in vivo through growth studies and in vitro by enzyme assay. Since, the expression of this gene occurs independent of its orientation within the chimeric plasmid, the 1.76 kb fragment may contain functional regulatory sequences in addition to the structural sequences for yeast dihydrofolate reductase.


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