Westholm Jakub Orzechowski, Nordberg Niklas, Murén Eva, Ameur Adam, Komorowski Jan, Ronne Hans
The Linnaeus Centre for Bioinformatics, Uppsala University, Box 598, SE-751 24 Uppsala, Sweden.
BMC Genomics. 2008 Dec 16;9:601. doi: 10.1186/1471-2164-9-601.
Expression of a large number of yeast genes is repressed by glucose. The zinc finger protein Mig1 is the main effector in glucose repression, but yeast also has two related proteins: Mig2 and Mig3. We have used microarrays to study global gene expression in all possible combinations of mig1, mig2 and mig3 deletion mutants.
Mig1 and Mig2 repress a largely overlapping set of genes on 2% glucose. Genes that are upregulated in a mig1 mig2 double mutant were grouped according to the contribution of Mig2. Most of them show partially redundant repression, with Mig1 being the major repressor, but some genes show complete redundancy, and some are repressed only by Mig1. Several redundantly repressed genes are involved in phosphate metabolism. The promoters of these genes are enriched for Pho4 sites, a novel GGGAGG motif, and a variant Mig1 site which is absent from genes repressed only by Mig1. Genes repressed only by Mig1 on 2% glucose include the hexose transporter gene HXT4, but Mig2 contributes to HXT4 repression on 10% glucose. HXT6 is one of the few genes that are more strongly repressed by Mig2. Mig3 does not seem to overlap in function with Mig1 and Mig2. Instead, Mig3 downregulates the SIR2 gene encoding a histone deacetylase involved in gene silencing and the control of aging.
Mig2 fine-tunes glucose repression by targeting a subset of the Mig1-repressed genes, and by responding to higher glucose concentrations. Mig3 does not target the same genes as Mig1 and Mig2, but instead downregulates the SIR2 gene.
大量酵母基因的表达受到葡萄糖的抑制。锌指蛋白Mig1是葡萄糖抑制作用的主要效应因子,但酵母中还有另外两种相关蛋白:Mig2和Mig3。我们利用微阵列研究了mig1、mig2和mig3缺失突变体所有可能组合中的全基因组基因表达情况。
在2%葡萄糖条件下,Mig1和Mig2抑制的基因集在很大程度上重叠。在mig1 mig2双突变体中上调的基因根据Mig2的作用进行了分组。其中大多数基因表现出部分冗余抑制,Mig1是主要抑制因子,但有些基因表现出完全冗余,还有一些基因仅受Mig1抑制。几个被冗余抑制的基因参与了磷酸盐代谢。这些基因的启动子富含Pho4位点、一种新的GGGAGG基序以及一个仅受Mig1抑制的基因中不存在的Mig1位点变体。在2%葡萄糖条件下仅受Mig1抑制的基因包括己糖转运蛋白基因HXT4,但Mig2在10%葡萄糖条件下对HXT4的抑制有作用。HXT6是少数受Mig2更强抑制的基因之一。Mig3的功能似乎与Mig1和Mig2不重叠。相反,Mig3下调了编码参与基因沉默和衰老调控的组蛋白脱乙酰酶的SIR2基因。
Mig2通过靶向Mig1抑制基因的一个子集并响应更高的葡萄糖浓度来微调葡萄糖抑制作用。Mig3靶向的基因与Mig1和Mig2不同,而是下调SIR2基因。