Abstract

In the present study, we have compared the expression level of the genes encoding the viral Hepatitis B S and preS2 using two different yeast vectors, a constitutive one (YepIPT) and a galactose-inducible one (YepDP1–8). We showed that the S and preS2 mRNAs were present in equivalent amounts in both systems, while the corresponding proteins showed a different pattern. The S and preS2 proteins were efficiently produced after galactose induction. However, under the constitutive promoter, the S protein was synthesized at the same level in presence of 2% glucose or galactose whereas the preS2 protein was efficiently synthesized on galactose but absent on 2% glucose. The substitution of glucose by non-repressive carbon sources such as 2% galactose, ethanol or glycerol led to a significant expression of preS2. A high level of preS2 expression was also achieved by lowering the glucose concentration. Our data suggest that glucose exerts a concentration dependent negative translational control on the preS2 mRNA.

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