XXIth YGM Conference
Göteborg, Sweden
July 7-12th, 2003

Conference Web Site ( http://www.yeast2003.se )

Abstract 10-54 Quantitative RT-PCR as a tool to study dynamic expression response after glucose pulse to ethanol grown cells.
Karin Otterstedt (1), Anders Stålberg (1), Christer Larsson (1), Stefan Hohmann (2), Lena Gustafsson (1)
(1) Molecular Biotechnology, Chalmers University, Box 462, Göteborg, 405 30, Sweden (karin.otterstedt@molbiotech.chalmers.se); (2) Department of Cell and Molecular Biology, Göteborg University, Sweden

For long researchers have been searching for the triggering signal/s for glucose repression. There is probably not only one signal and different genes will be the target for different signals. It has previously been shown that glucose repression of some genes are correlated to glycolytic rate. Into a strain where all the glucose transporters have been deleted (Null strain) chimeras of the low and high affinity transporters HXT1 and HXT7 have been expressed one at a time. These strains have given us a series of strains with different glucose consumption rates i.e glycolytic rates (see poster 12-34). In this study we have initially been looking at three strains: Wild type, HXT7 only expressing strain and the Null strain. By growing these strains on ethanol and then pulse them with 5% glucose we have followed the dynamic expression response of genes exposed to glucose repression and induction using real-time PCR as a fast, reliable and sensitive method.


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