Westergaard Steen L, Bro Christoffer, Olsson Lisbeth, Nielsen Jens
Center for Microbial Biotechnology, BioCentrum-DTU, Technical University of Denmark, Building 223, DK-2800 Kgs. Lyngby, Denmark.
FEMS Yeast Res. 2004 Dec;5(3):193-204. doi: 10.1016/j.femsyr.2004.06.013.
The role of Grr1p in glucose sensing in Saccharomyces cerevisiae was elucidated through genome-wide transcription analysis. From triplicate analysis of a strain with deletion of the GRR1-gene from the genome and an isogenic reference strain, 68 genes were identified to have significantly altered expression using a Student's t-test with Bonferroni correction. These 68 genes were widely distributed across different parts of the cellular metabolism and GRR1-deletion is therefore concluded to result in polytrophic effects, indicating multiple roles for Grr1p. Using a less conservative statistical test, namely the SAM test, 232 genes were identified as having significantly altered expression, and also these genes were widely distributed across different parts of the cellular metabolism. Promoter analyses on a genome-wide scale and on the genes with significant changes revealed an over-representation of DNA-binding motifs for the transcriptional regulators Mig1p and Rgt1p in the promoter region of the significantly altered genes, indicating that Grr1p plays an important role in the regulatory pathways that ultimately lead to transcriptional regulation by each of the components Mig1p and Rgt1p.
通过全基因组转录分析阐明了酿酒酵母中Grr1p在葡萄糖感知中的作用。对基因组中GRR1基因缺失的菌株和同基因参考菌株进行三次重复分析,使用经Bonferroni校正的学生t检验,鉴定出68个基因的表达有显著变化。这68个基因广泛分布于细胞代谢的不同部分,因此得出结论,GRR1缺失会导致多效性效应,表明Grr1p具有多种作用。使用一种不太保守的统计检验,即SAM检验,鉴定出232个基因的表达有显著变化,这些基因也广泛分布于细胞代谢的不同部分。在全基因组范围内以及对有显著变化的基因进行启动子分析,结果显示在显著改变基因的启动子区域,转录调节因子Mig1p和Rgt1p的DNA结合基序出现超量表达,这表明Grr1p在最终导致Mig1p和Rgt1p各自进行转录调节的调控途径中发挥重要作用。