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Quantitative RNA-seq analysis of the Campylobacter jejuni transcriptome
Author(s) -
Roy R. Chaudhuri,
Lu Yu,
Alpa Kanji,
Timothy T. Perkins,
Paul P. Gardner,
Jyoti S. Choudhary,
Duncan J. Maskell,
Andrew J. Grant
Publication year - 2011
Publication title -
microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 179
eISSN - 1465-2080
pISSN - 1350-0872
DOI - 10.1099/mic.0.050278-0
Subject(s) - biology , transcriptome , rna seq , computational biology , campylobacter jejuni , rpon , regulon , genetics , gene , gene expression , bacteria , promoter
Campylobacter jejuni is the most common bacterial cause of foodborne disease in the developed world. Its general physiology and biochemistry, as well as the mechanisms enabling it to colonize and cause disease in various hosts, are not well understood, and new approaches are required to understand its basic biology. High-throughput sequencing technologies provide unprecedented opportunities for functional genomic research. Recent studies have shown that direct Illumina sequencing of cDNA (RNA-seq) is a useful technique for the quantitative and qualitative examination of transcriptomes. In this study we report RNA-seq analyses of the transcriptomes of C. jejuni (NCTC11168) and its rpoN mutant. This has allowed the identification of hitherto unknown transcriptional units, and further defines the regulon that is dependent on rpoN for expression. The analysis of the NCTC11168 transcriptome was supplemented by additional proteomic analysis using liquid chromatography-MS. The transcriptomic and proteomic datasets represent an important resource for the Campylobacter research community.

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