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基于转录谱分析鉴定受agr和/或sarA基因座调控的金黄色葡萄球菌基因。

Transcription profiling-based identification of Staphylococcus aureus genes regulated by the agr and/or sarA loci.

作者信息

Dunman P M, Murphy E, Haney S, Palacios D, Tucker-Kellogg G, Wu S, Brown E L, Zagursky R J, Shlaes D, Projan S J

机构信息

Infectious Diseases, Wyeth-Ayerst Research, Pearl River, New York 10965, USA.

出版信息

J Bacteriol. 2001 Dec;183(24):7341-53. doi: 10.1128/JB.183.24.7341-7353.2001.

Abstract

The advent of transcription profiling technologies has provided researchers with an unprecedented ability to study biological processes. Accordingly, a custom-made Affymetrix GeneChip, constituting >86% of the Staphylococcus aureus genome, was used to identify open reading frames that are regulated by agr and/or SarA, the two best-studied regulators of the organism's virulence response. RNA extracted from wild-type cells and agr, sarA, and agr sarA mutant cells in the early-, mid-, and late-log and stationary phases of growth was analyzed. Open reading frames with transcription patterns expected of genes either up- or downregulated in an agr- and/or SarA-dependent manner were identified. Oligonucleotide microarray and Northern blot analyses confirmed that the transcription of several known virulence genes, including hla (alpha-toxin) and spa (protein A), is regulated by each effector and provided insights about the regulatory cascades involved in both alpha-hemolysin and protein A expression. Several putative virulence factors were also identified as regulated by agr and/or SarA. In addition, genes that are involved in several biological processes but which are difficult to reconcile as playing a direct role in the organism's pathogenesis also appeared to be regulated by each effector, suggesting that products of both the agr and the sarA locus are more-global transcription regulators than previously realized.

摘要

转录谱分析技术的出现为研究人员提供了前所未有的研究生物过程的能力。因此,一种定制的Affymetrix基因芯片(覆盖超过86%的金黄色葡萄球菌基因组)被用于鉴定受agr和/或SarA调控的开放阅读框,这两个是该生物体毒力反应中研究得最深入的调控因子。分析了从野生型细胞以及处于生长对数期早期、中期、晚期和稳定期的agr、sarA和agr sarA突变体细胞中提取的RNA。鉴定出了具有预期转录模式的开放阅读框,这些基因以依赖agr和/或SarA的方式上调或下调。寡核苷酸微阵列和Northern印迹分析证实,包括hla(α毒素)和spa(蛋白A)在内的几个已知毒力基因的转录受每个效应因子调控,并提供了有关α溶血素和蛋白A表达所涉及的调控级联的见解。还鉴定出了几个推定的毒力因子受agr和/或SarA调控。此外,参与几个生物过程但难以协调其在生物体发病机制中直接作用的基因似乎也受每个效应因子调控,这表明agr和sarA基因座的产物是比以前认识到的更具全局性的转录调节因子。

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