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氮同化因子 sigma54 的启动子和调控区分析揭示了大肠杆菌 MG1655 鞭毛生物合成的替代策略。

Promoter and regulon analysis of nitrogen assimilation factor, sigma54, reveal alternative strategy for E. coli MG1655 flagellar biosynthesis.

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, WI 53706, USA.

出版信息

Nucleic Acids Res. 2010 Mar;38(4):1273-83. doi: 10.1093/nar/gkp1123. Epub 2009 Dec 6.

Abstract

Bacteria core RNA polymerase (RNAP) must associate with a sigma factor to recognize promoter sequences. Promoters recognized by the sigma(54) (or sigma(N)) associated RNA polymerase are unique in having conserved positions around -24 and -12 nucleotides upstream from the transcriptional start site. Using DNA microarrays representing the entire Escherichia coli genome and promoter validation approaches, we identify 40 in vivo targets of sigma(54), the nitrogen assimilation sigma factor, and estimate that there are 70 sigma(54) promoters in total. Immunoprecipitation assays have been performed to further evaluate the efficiency of our approaches. In addition, promoter consensus binding search and primer extension assay helped us to identify a new sigma(54) promoter carried by insB-5 in the upstream of flhDC operon. The involvement of sigma(54) in flagellar biosynthesis in sequenced E. coli strain MG1655 indicates a fluid gene regulation phenomenon carried by some mobile elements in bacteria genome.

摘要

细菌核心 RNA 聚合酶(RNAP)必须与 sigma 因子结合才能识别启动子序列。与 sigma(54)(或 sigma(N))相关的 RNA 聚合酶识别的启动子在转录起始位点上游的-24 和-12 个核苷酸处具有保守位置,这是独特的。我们使用代表整个大肠杆菌基因组的 DNA 微阵列和启动子验证方法,鉴定了 40 个 sigma(54)(氮同化 sigma 因子)的体内靶标,并估计总共有 70 个 sigma(54)启动子。免疫沉淀测定已被用于进一步评估我们的方法的效率。此外,启动子共识结合搜索和引物延伸测定帮助我们确定了在 flhDC 操纵子上游的 insB-5 中携带的一个新的 sigma(54)启动子。sigma(54)在已测序的大肠杆菌菌株 MG1655 中的鞭毛生物合成中的参与表明了细菌基因组中的一些移动元件所携带的动态基因调控现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b80c/2831329/f7acd3cca8ea/gkp1123f1.jpg

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