Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10769921 | Biochemical and Biophysical Research Communications | 2005 | 9 Pages |
Abstract
The Saccharomyces cerevisiae JEN1 gene encoding the lactate transporter undergoes strong catabolic repression at both transcriptional and post-transcriptional levels. JEN1 mRNA decay is greatly accelerated upon the addition of a pulse of glucose, fructose or mannose to induced cell cultures. Mapping of the 5â²UTRs and 3â²UTRs of JEN1 transcripts revealed multiple transcription start-sites located at position â51, +391 or +972, depending on the cell culture conditions. The presence of the JEN1(+391) transcript correlated with rapid glucose-triggered mRNA degradation of the JEN1(â51) transcript, whereas when the small transcript started at position +972, the JEN1(â51) mRNA turnover rate was unaffected. Overexpressed JEN1(+391) transcript accelerated JEN1(â51) mRNA decay in all conditions tested but was not translated. We propose that the JEN1(+391) transcript may have a “sensor-like” function, regulating glucose-triggered degradation of JEN1(â51) protein-coding mRNA.
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Authors
R.P. Andrade, P. Kötter, K.-D. Entian, M. Casal,