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利用序列和基因表达信息对嗜硫地杆菌中RpoS和RpoD调控位点进行计算预测。

Computational prediction of RpoS and RpoD regulatory sites in Geobacter sulfurreducens using sequence and gene expression information.

作者信息

Yan Bin, Núñez Cinthia, Ueki Toshiyuki, Esteve-Núñez Abraham, Puljic Marko, Adkins Ronald M, Methé Barbara A, Lovley Derek R, Krushkal Julia

机构信息

Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, 38163, USA.

出版信息

Gene. 2006 Dec 15;384:73-95. doi: 10.1016/j.gene.2006.06.025. Epub 2006 Jul 20.

Abstract

RpoS, the sigma S subunit of RNA polymerase, is vital during the growth and survival of Geobacter sulfurreducens under conditions typically encountered in its native subsurface environments. We investigated the conservation of sites that may be important for RpoS function in G. sulfurreducens. We also employed sequence information and expression microarray data to predict G. sulfurreducens genome sites that may be related to RpoS regulation. Hierarchical clustering identified three clusters of significantly downregulated genes in the rpoS deletion mutant. The search for conserved overrepresented motifs in co-regulated operons identified likely -35 and -10 promoter elements upstream of a number of functionally important G. sulfurreducens operons that were downregulated in the rpoS deletion mutant. Putative -35/-10 promoter elements were also identified in the G. sulfurreducens genome using sequence similarity searches to matrices of -35/-10 promoter elements found in G. sulfurreducens and in Escherichia coli. Due to a sufficient degree of sequence similarity between -35/-10 promoter elements for RpoS, RpoD, and other sigma factors, both the sequence similarity searches and the search for conserved overrepresented motifs using microarray data may identify promoter elements for both RpoS and other sigma factors.

摘要

RpoS是RNA聚合酶的σS亚基,在嗜硫地杆菌在其原生地下环境中通常遇到的条件下的生长和存活过程中至关重要。我们研究了嗜硫地杆菌中可能对RpoS功能重要的位点的保守性。我们还利用序列信息和表达微阵列数据来预测嗜硫地杆菌基因组中可能与RpoS调控相关的位点。层次聚类分析确定了rpoS缺失突变体中显著下调的三个基因簇。在共调控操纵子中寻找保守的过度表达基序,发现在rpoS缺失突变体中下调的许多功能重要的嗜硫地杆菌操纵子上游可能存在-35和-10启动子元件。利用与嗜硫地杆菌和大肠杆菌中发现的-35/-10启动子元件矩阵的序列相似性搜索,在嗜硫地杆菌基因组中也鉴定出了假定的-35/-10启动子元件。由于RpoS、RpoD和其他σ因子的-35/-10启动子元件之间存在足够程度的序列相似性,序列相似性搜索和利用微阵列数据寻找保守的过度表达基序都可能识别出RpoS和其他σ因子的启动子元件。

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