Williams Roy M, Primig Michael, Washburn Brian K, Winzeler Elizabeth A, Bellis Michel, Sarrauste de Menthiere Cyril, Davis Ronald W, Esposito Rochelle E
Department of Molecular Genetics and Cell Biology, University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13431-6. doi: 10.1073/pnas.202495299. Epub 2002 Oct 7.
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 SK1) 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 SK1 is better adapted to respiration and W303 to fermentation, which may in part account for the more efficient and synchronous sporulation of SK1.
已知酵母中的Ume6转录因子在生长和减数分裂发育过程中既能抑制也能激活多种基因的表达。为了更全面地了解该蛋白所调控的功能,利用微阵列分析来检测野生型和ume6Delta二倍体在葡萄糖和乙酸盐营养生长期间的转录情况。研究了两种不同的遗传背景(W303和SK1),以确定一组不依赖菌株的Ume6调控基因的核心集。在两种背景下其表达均受Ume6控制的基因中,82个与Ume6结合位点(URS1)具有同源性,预计将由Ume6直接调控。其中绝大多数已知功能的基因参与碳/氮代谢和/或减数分裂。大约一半的Ume6直接靶标在减数分裂期间被诱导,大多数属于减数分裂早期表达类别(簇4),较小的一部分属于中期和后期类别(簇5 - 7)。基于这些数据,我们提出Ume6在二倍体细胞中发挥独特作用,将对营养信号的代谢反应与减数分裂的起始和进程联系起来。最后,两种遗传背景下的表达模式表明,SK1更适应呼吸作用,而W303更适应发酵作用,这可能部分解释了SK1更高效且同步的孢子形成。