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枯草芽孢杆菌S10核糖体蛋白基因簇分析鉴定出两个启动子,它们可能负责整个15千碱基的S10-spc-alpha簇的转录。

Analysis of the Bacillus subtilis S10 ribosomal protein gene cluster identifies two promoters that may be responsible for transcription of the entire 15-kilobase S10-spc-alpha cluster.

作者信息

Li X, Lindahl L, Sha Y, Zengel J M

机构信息

Department of Biological Sciences, University of Maryland Baltimore County, Baltimore 21250, USA.

出版信息

J Bacteriol. 1997 Nov;179(22):7046-54. doi: 10.1128/jb.179.22.7046-7054.1997.

Abstract

We have sequenced a previously uncharacterized region of the Bacillus subtilis S10 ribosomal protein gene cluster. The new segment includes genes for S10, L3, L4, L23, L2, S19, L22, S3, and part of L16. These B. subtilis genes map in the same order as the genes in the Escherichia coli S10 ribosomal protein operon. Two potential promoter sequences were identified, one approximately 200 bases and the other approximately 140 bases upstream of the S10 gene. The activities of the two promoters were demonstrated by primer extension analysis, in vitro transcription experiments, and in vivo promoter fusion plasmid studies. In agreement with previous reports, our Northern analysis of exponentially growing cells failed to identify terminators or other active promoters within the S10-spc-alpha region. Our observations suggest that the two S10 promoters reported here are responsible for transcribing a 15-kb-long transcript for all of the genes in the B. subtilis S10, spc, and alpha clusters.

摘要

我们对枯草芽孢杆菌S10核糖体蛋白基因簇中一个此前未被表征的区域进行了测序。新片段包括S10、L3、L4、L23、L2、S19、L22、S3以及L16部分的基因。这些枯草芽孢杆菌基因的排列顺序与大肠杆菌S10核糖体蛋白操纵子中的基因相同。鉴定出了两个潜在的启动子序列,一个在S10基因上游约200个碱基处,另一个在其上游约140个碱基处。通过引物延伸分析、体外转录实验和体内启动子融合质粒研究证实了这两个启动子的活性。与之前的报道一致,我们对指数生长细胞的Northern分析未能在S10-spc-alpha区域内鉴定出终止子或其他活性启动子。我们的观察结果表明,此处报道的两个S10启动子负责转录一个15 kb长的转录本,该转录本包含枯草芽孢杆菌S10、spc和alpha基因簇中的所有基因。

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