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高分辨率分析肺炎链球菌转录组在广泛的感染相关条件下。

High-resolution analysis of the pneumococcal transcriptome under a wide range of infection-relevant conditions.

机构信息

Molecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Centre for Synthetic Biology, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands.

Department of Fundamental Microbiology, Faculty of Biology and Medicine, University of Lausanne, Biophore Building, CH-1015 Lausanne, Switzerland.

出版信息

Nucleic Acids Res. 2018 Nov 2;46(19):9990-10006. doi: 10.1093/nar/gky750.

Abstract

Streptococcus pneumoniae is an opportunistic human pathogen that typically colonizes the nasopharyngeal passage and causes lethal disease in other host niches, such as the lung or the meninges. The expression and regulation of pneumococcal genes at different life-cycle stages, such as commensal or pathogenic, are not entirely understood. To chart the transcriptional responses of S. pneumoniae, we used RNA-seq to quantify the relative abundance of the transcriptome under 22 different infection-relevant conditions. The data demonstrated a high level of dynamic expression and, strikingly, all annotated pneumococcal genomic features were expressed in at least one of the studied conditions. By computing the correlation values of every pair of genes across all studied conditions, we created a co-expression matrix that provides valuable information on both operon structure and regulatory processes. The co-expression data are highly consistent with well-characterized operons and regulons, such as the PyrR, ComE and ComX regulons, and have allowed us to identify a new member of the competence regulon. Lastly, we created an interactive data center named PneumoExpress (https://veeninglab.com/pneumoexpress) that enables users to access the expression data as well as the co-expression matrix in an intuitive and efficient manner, providing a valuable resource to the pneumococcal research community.

摘要

肺炎链球菌是一种机会性人类病原体,通常定植于鼻咽部,并在肺部或脑膜等其他宿主部位引起致命性疾病。肺炎链球菌在不同生命周期阶段(如共生或致病)的基因表达和调控尚未完全清楚。为了绘制肺炎链球菌的转录反应图谱,我们使用 RNA-seq 技术来量化在 22 种不同感染相关条件下转录组的相对丰度。这些数据表明了高水平的动态表达,而且令人惊讶的是,所有注释的肺炎链球菌基因组特征都在至少一种研究条件下表达。通过计算所有研究条件下每对基因的相关值,我们创建了一个共表达矩阵,该矩阵提供了有关操纵子结构和调控过程的有价值信息。共表达数据与已充分表征的操纵子和调控子高度一致,如 PyrR、ComE 和 ComX 调控子,并且使我们能够鉴定出一个新的感受态调控子成员。最后,我们创建了一个名为 PneumoExpress 的交互式数据中心(https://veeninglab.com/pneumoexpress),用户可以直观高效地访问表达数据和共表达矩阵,为肺炎链球菌研究界提供了有价值的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b8/6212715/30e7dedba20b/gky750fig1.jpg

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