Rodríguez Sonia, Santamaría Ramón I, Fernández-Abalos Jose Manuel, Díaz Margarita
Instituto de Microbiología Bioquímica/Departamento de Microbiología y Genética, Consejo Superior de Investigaciones Científicas (CSIC)/Universidad de Salamanca, Edificio Departamental, Campus Miguel de Unamuno, Salamanca, Spain.
Gene. 2005 May 23;351:1-9. doi: 10.1016/j.gene.2005.03.007. Epub 2005 Apr 22.
The expression of xysA, a gene encoding for an endoxylanase from Streptomyces halstedii JM8, is repressed by glucose. In order to define the regions involved in its regulation, several deletions were made in the 475 bp xysA promoter and were studied using the melC operon from S. glaucescens as a reporter. Four of the deleted versions obtained were seen to be derepressed when driving melC or its own xysA gene expression in Streptomyces lividans. Quantitative assays revealed that the activity of xylanase produced under the control of these four deleted promoters was higher than the original one in the presence of glucose. Three regions - RI, R16 and R21 - involved in glucose repression were defined in this analysis: RI is a palindromic sequence that is highly conserved among xylanase gene promoters from Actinomycetes (-213 GAAAxxTTTCxGAAA -197) and, R16 and R21 define two new seven-pair conserved motifs, respectively (-113 5'-CCTTCCC-3' -106 in R16 and -76 5'-CGAACGG-3' -69 in R21) located in the untranslated mRNA. Gel shift assays demonstrated the existence of proteins that bind specifically to these regions.
来自哈氏链霉菌JM8的木聚糖内切酶编码基因xysA的表达受葡萄糖抑制。为了确定参与其调控的区域,对475 bp的xysA启动子进行了多处缺失,并以青灰链霉菌的melC操纵子作为报告基因进行研究。当在淡紫链霉菌中驱动melC或其自身的xysA基因表达时,发现获得的四个缺失版本的表达不再受抑制。定量分析表明,在葡萄糖存在的情况下,由这四个缺失启动子控制产生的木聚糖酶活性高于原始启动子。在此分析中确定了三个参与葡萄糖抑制的区域——RI、R16和R21:RI是一个回文序列,在放线菌的木聚糖酶基因启动子中高度保守(-213 GAAAxxTTTCxGAAA -197),R16和R21分别定义了两个新的七碱基对保守基序(R16中为-113 5'-CCTTCCC-3' -106,R21中为-76 5'-CGAACGG-3' -69),位于未翻译的mRNA中。凝胶迁移实验证明存在与这些区域特异性结合的蛋白质。