The Ume6 regulon coordinates metabolic and meiotic gene expression in yeast

被引:94
作者
Williams, RM
Primig, M
Washburn, BK
Winzeler, EA
Bellis, M
de Menthière, CS
Davis, RW
Esposito, RE
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[2] CNRS, UPR 1086, Ctr Rech Biochim Macromol, F-34293 Montpellier, France
[3] CNRS, UPR 1142, Inst Genet Humaine, F-34396 Montpellier, France
[4] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
关键词
D O I
10.1073/pnas.202495299
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Ume6 transcription factor in yeast is known to both repress and activate expression of diverse genes during growth and meiotic development. To obtain a more complete profile of the functions regulated by this protein, microarray analysis was used to examine transcription in wild-type and ume6Delta diploids during vegetative growth in glucose and acetate. Two different genetic backgrounds (W303 and SKI) were examined to identify a core set of strain-independent Ume6-regulated genes. Among genes whose expression is controlled by Ume6 in both backgrounds, 82 contain homologies to the Ume6-binding site (URS1) and are expected to be directly regulated by Ume6. The vast majority of those whose functions are known participate in carbon/nitrogen metabolism and/or meiosis. Approximately half of the Ume6 direct targets are induced during meiosis, with most falling into the early meiotic expression class (cluster 4), and a smaller subset in the middle and later classes (clusters 5-7). Based on these data, we propose that Ume6 serves a unique role in diploid cells, coupling metabolic responses to nutritional cues with the initiation and progression of meiosis. Finally, expression patterns in the two genetic backgrounds suggest that SKI is better adapted to respiration and W303 to fermentation, which may in part account for the more efficient and synchronous sporulation of SKI.
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页码:13431 / 13436
页数:6
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