Multiple transcripts regulate glucose-triggered mRNA decay of the lactate transporter JEN1 from Saccharomyces cerevisiae

被引:27
作者
Andrade, RP
Kötter, P
Entian, KD
Casal, M
机构
[1] Univ Minho, Dept Biol, Ctr Biol, P-4710057 Braga, Portugal
[2] Goethe Univ Frankfurt, Inst Mikrobiol, D-60439 Frankfurt, Germany
[3] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst, ICVS, P-4710057 Braga, Portugal
关键词
yeast; mRNA degradation; gulcose repression; JEN1;
D O I
10.1016/j.bbrc.2005.04.119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 5'UTRs and 3'UTRs of JEN1 transcripts revealed multiple transcription start-sites located at position -51, +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(-51) transcript, whereas when the small transcript started at position +972, the JEN1(-51) mRNA turnover rate was unaffected. Overexpressed JEN1(+391) transcript accelerated JEN1(-51) 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(-51) protein-coding mRNA. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:254 / 262
页数:9
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