Abella Marc, Rodríguez Sonia, Paytubi Sonia, Campoy Susana, White Malcolm F, Barbé Jordi
Departament de Genètica i Microbiologia, Universitat Autònoma de Barcelona 08193 Bellaterra, Spain.
Nucleic Acids Res. 2007;35(20):6788-97. doi: 10.1093/nar/gkm782. Epub 2007 Oct 5.
Little is known about the regulation of the DNA damage-mediated gene expression in archaea. Here we report that the addition of actinomycin D to Sulfolobus solfataricus cultures triggers the expression of the radA paralogue sso0777. Furthermore, a specific retarded band is observed when electrophoretic mobility shift assays (EMSAs) with crude S. solfataricus cell extracts and the sso0777 promoter were carried out. The protein that binds to this promoter was isolated and identified as Sta1. Footprinting experiments have shown that the Sta1 DNA-binding site is included in the ATTTTTTATTTTCACATGTAAGATGTTTATT sequence, which is located upstream the putative TTG translation starting codon of the sso0777 gene. Additionally, gel electrophoretic mobility retardation experiments using mutant sso0777 promoter derivatives show the presence of three essential motifs (TTATT, CANGNA and TTATT) that are absolutely required for Sta1 DNA binding. Finally, in vitro transcription experiments confirm that Sta1 functions as an activator for sso0777 gene expression being the first identified archaeal regulatory protein associated with the DNA damage-mediated induction of gene expression.
关于古菌中DNA损伤介导的基因表达调控,人们了解甚少。在此我们报道,向嗜热栖热菌培养物中添加放线菌素D会触发radA旁系同源物sso0777的表达。此外,当用嗜热栖热菌细胞粗提物和sso0777启动子进行电泳迁移率变动分析(EMSA)时,观察到一条特定的滞后带。与该启动子结合的蛋白质被分离并鉴定为Sta1。足迹实验表明,Sta1的DNA结合位点包含在ATTTTTTATTTTCACATGTAAGATGTTTATT序列中,该序列位于sso0777基因假定的TTG翻译起始密码子上游。此外,使用突变的sso0777启动子衍生物进行的凝胶电泳迁移率阻滞实验表明,存在三个对Sta1与DNA结合绝对必需的基本基序(TTATT、CANGNA和TTATT)。最后,体外转录实验证实,Sta1作为sso0777基因表达的激活因子发挥作用,它是首个被鉴定出的与DNA损伤介导的基因表达诱导相关的古菌调节蛋白。