Proft Markus, Gibbons Francis D, Copeland Matthew, Roth Frederick P, Struhl Kevin
Department Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Eukaryot Cell. 2005 Aug;4(8):1343-52. doi: 10.1128/EC.4.8.1343-1352.2005.
In Saccharomyces cerevisiae, the ATF/CREB transcription factor Sko1 (Acr1) regulates the expression of genes induced by osmotic stress under the control of the high osmolarity glycerol (HOG) mitogen-activated protein kinase pathway. By combining chromatin immunoprecipitation and microarrays containing essentially all intergenic regions, we estimate that yeast cells contain approximately 40 Sko1 target promoters in vivo; 20 Sko1 target promoters were validated by direct analysis of individual loci. The ATF/CREB consensus sequence is not statistically overrepresented in confirmed Sko1 target promoters, although some sites are evolutionarily conserved among related yeast species, suggesting that they are functionally important in vivo. These observations suggest that Sko1 association in vivo is affected by factors beyond the protein-DNA interaction defined in vitro. Sko1 binds a number of promoters for genes directly involved in defense functions that relieve osmotic stress. In addition, Sko1 binds to the promoters of genes encoding transcription factors, including Msn2, Mot3, Rox1, Mga1, and Gat2. Stress-induced expression of MSN2, MOT3, and MGA1 is diminished in sko1 mutant cells, while transcriptional regulation of ROX1 seems to be unaffected. Lastly, Sko1 targets PTP3, which encodes a phosphatase that negatively regulates Hog1 kinase activity, and Sko1 is required for osmotic induction of PTP3 expression. Taken together our results suggest that Sko1 operates a transcriptional network upon osmotic stress, which involves other specific transcription factors and a phosphatase that regulates the key component of the signal transduction pathway.
在酿酒酵母中,ATF/CREB转录因子Sko1(Acr1)在高渗甘油(HOG)丝裂原活化蛋白激酶途径的控制下,调节由渗透胁迫诱导的基因的表达。通过结合染色质免疫沉淀和包含基本上所有基因间区域的微阵列,我们估计酵母细胞在体内含有大约40个Sko1靶启动子;通过对单个位点的直接分析验证了20个Sko1靶启动子。尽管在相关酵母物种中一些位点在进化上是保守的,表明它们在体内功能上很重要,但在已确认的Sko1靶启动子中,ATF/CREB共有序列在统计学上并未过度富集。这些观察结果表明,Sko1在体内的结合受到体外定义的蛋白质-DNA相互作用之外的因素的影响。Sko1结合许多直接参与缓解渗透胁迫的防御功能基因的启动子。此外,Sko1结合编码转录因子的基因的启动子,包括Msn2、Mot3、Rox1、Mga1和Gat2。在sko1突变细胞中,MSN2、MOT3和MGA1的应激诱导表达减少,而ROX1的转录调控似乎不受影响。最后,Sko1靶向PTP3,PTP3编码一种负调节Hog1激酶活性的磷酸酶,并且Sko1是PTP3表达的渗透诱导所必需的。综合我们所有的结果表明,Sko1在渗透胁迫时运作一个转录网络,该网络涉及其他特定转录因子和一个调节信号转导途径关键组分的磷酸酶。