Schwer Beate, Sanchez Ana M, Garg Angad, Chatterjee Debashree, Shuman Stewart
Department of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA
Department of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
mBio. 2017 Aug 15;8(4):e01218-17. doi: 10.1128/mBio.01218-17.
Fission yeast phosphate homeostasis entails transcriptional induction of genes encoding phosphate-mobilizing proteins under conditions of phosphate starvation. Transcription factor Pho7, a member of the ZnCys family of fungal transcription regulators, is the central player in the starvation response. The DNA binding sites in the promoters of phosphate-responsive genes have not been defined, nor have any structure-function relationships been established for the Pho7 protein. Here we narrow this knowledge gap by (i) delineating an autonomous DNA-binding domain (DBD) within Pho7 that includes the ZnCys module, (ii) deploying recombinant Pho7 DBD in DNase I footprinting and electrophoretic mobility shift assays (EMSAs) to map the Pho7 recognition sites in the promoters of the phosphate-regulated and genes to a 12-nucleotide sequence motif [5'-TCG(G/C)(A/T)xxTTxAA], (iii) independently identifying the same motif as a Pho7 recognition element via analysis of available genome-wide ChIP-seq data, (iv) affirming that mutations in the two Pho7 recognition sites in the promoter efface expression , and (v) establishing that the zinc-binding cysteines and a pair of conserved arginines in the DBD are essential for Pho7 activity Fungi respond to phosphate starvation by inducing the transcription of a set of phosphate acquisition genes that comprise a phosphate regulon. Pho7, a member of the ZnCys family of fungal transcription regulators, is the central player in the phosphate starvation response in fission yeast. The present study identifies a 12-nucleotide Pho7 DNA binding motif [5'-TCG(G/C)(A/T)xxTTxAA] in the promoters of phosphate-regulated genes, pinpoints DNA and protein features important for Pho7 binding to DNA, and correlates them with Pho7-dependent gene expression The results highlight distinctive properties of Pho7 vis-a-vis other fungal zinc binuclear cluster transcription factors as well as the divergent cast of transcription factors deployed for phosphate homeostasis in fission yeast versus budding yeast.
裂殖酵母的磷酸盐稳态需要在磷酸盐饥饿条件下对编码磷酸盐动员蛋白的基因进行转录诱导。转录因子Pho7是真菌转录调节因子ZnCys家族的成员,是饥饿反应的核心参与者。磷酸盐反应基因启动子中的DNA结合位点尚未确定,Pho7蛋白的任何结构-功能关系也未建立。在这里,我们通过以下方式缩小了这一知识差距:(i)在Pho7中描绘一个自主的DNA结合结构域(DBD),其中包括ZnCys模块;(ii)在DNA酶I足迹分析和电泳迁移率变动分析(EMSA)中部署重组Pho7 DBD,以将磷酸盐调节基因和基因启动子中的Pho7识别位点定位到一个12个核苷酸的序列基序[5'-TCG(G/C)(A/T)xxTTxAA];(iii)通过分析可用的全基因组ChIP-seq数据,独立地将相同的基序鉴定为Pho7识别元件;(iv)确认启动子中两个Pho7识别位点的突变消除了表达;(v)确定DBD中的锌结合半胱氨酸和一对保守的精氨酸对Pho7活性至关重要。真菌通过诱导一组构成磷酸盐调节子的磷酸盐获取基因的转录来应对磷酸盐饥饿。Pho7是真菌转录调节因子ZnCys家族的成员,是裂殖酵母中磷酸盐饥饿反应的核心参与者。本研究在磷酸盐调节基因的启动子中鉴定出一个12个核苷酸的Pho7 DNA结合基序[5'-TCG(G/C)(A/T)xxTTxAA],确定了Pho7与DNA结合重要的DNA和蛋白质特征,并将它们与Pho7依赖的基因表达相关联。结果突出了Pho7相对于其他真菌锌双核簇转录因子的独特特性,以及裂殖酵母与芽殖酵母中用于磷酸盐稳态的转录因子的不同类型。