利用定点突变分析白念珠菌依赖铁基因FRP1启动子元件  

Regulating Promoter Element of Iron-dependent Gene FRP1 in Candida albicans by Site-directed Mutation

作　　者：桂磊[1] 梁勇[1] 魏东盛[1] 郑雯[1] 邢来君[1] 李明春[1] 

机构地区：[1]南开大学微生物学系分子微生物学与技术教育部重点实验室,天津300071

出　　处：《生物工程学报》2008年第8期1348-1353,共6页Chinese Journal of Biotechnology

基　　金：国家自然科学基金(No.30570096);教育部博士点基金资助项目(No.20070055011);教育部留学回国人员科研启动基金(教外司留(2005)546号)~~

摘　　要：通过对白念珠菌高铁还原酶基因FRP1启动子进行突变分析,确认启动子中特殊调控元件。我们通过分析FRP1起始密码子上游1000bp序列发现在-160和-650处有2个推测的Rim101p结合位点,对其分别进行定点突变,然后构建启动子与报告基因LacZ融合质粒,转化整合到白念珠菌rim101-/-株和野生株中,检测不同缺铁条件下β-半乳糖苷酶活性。结果发现碱性条件,Rim101p能够正向调控FRP1的表达;启动子-160处突变对启动子功能影响较弱,而-650突变使启动子活性大大降低,此结果和双突变的结果相同,表明Rim101p主要通过与启动子-650处结合位点相互作用来调控FRP1的表达。Microarray analysis revealed that the expression of ferric reductase （FRP1） can be regulated by the Rim101 protein, In order to find new transcriptional regulatory element in the promoter of FRP1, we analyzed the 1000 bp sequence upstream of ATG to find 2 potential Rim101p binding sites. We generated site-specific mutations in each of the two sites and fused these mutated promoters to LacZ. Then the promoter-LacZ fusion construct was recombinant into wild type and rim101-/- strains for β- galactosidase assay. The results revealed that the FRP1 was up-regulated in alkaline pH and this was caused by iron starvation. The -650 site, not the -160 site, had an important role in FRP1 Riml01p-dependent expression. We conclude that Riml01p may interact with the -650 binding site of the promoter to regulate the FRP1 expression.

关 键 词：定点突变 白念珠菌 Rim101蛋白 高铁还原酶基因 

分 类 号：Q93[生物学—微生物学]