Transcriptome Analysis of Pseudomonas syringae Identifies New Genes, Noncoding RNAs, and Antisense Activity

Author:

Filiatrault Melanie J.12,Stodghill Paul V.1,Bronstein Philip A.12,Moll Simon2,Lindeberg Magdalen2,Grills George3,Schweitzer Peter3,Wang Wei3,Schroth Gary P.4,Luo Shujun4,Khrebtukova Irina4,Yang Yong1,Thannhauser Theodore1,Butcher Bronwyn G.2,Cartinhour Samuel12,Schneider David J.12

Affiliation:

1. U.S. Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853

2. Department of Plant Pathology and Plant-Microbe Biology, Cornell University, Ithaca, New York 14853

3. Life Sciences Core Laboratories Center, Cornell University, Ithaca, New York 14853

4. Illumina, Inc., Hayward, California 94545

Abstract

ABSTRACT To fully understand how bacteria respond to their environment, it is essential to assess genome-wide transcriptional activity. New high-throughput sequencing technologies make it possible to query the transcriptome of an organism in an efficient unbiased manner. We applied a strand-specific method to sequence bacterial transcripts using Illumina's high-throughput sequencing technology. The resulting sequences were used to construct genome-wide transcriptional profiles. Novel bioinformatics analyses were developed and used in combination with proteomics data for the qualitative classification of transcriptional activity in defined regions. As expected, most transcriptional activity was consistent with predictions from the genome annotation. Importantly, we identified and confirmed transcriptional activity in areas of the genome inconsistent with the annotation and in unannotated regions. Further analyses revealed potential RpoN-dependent promoter sequences upstream of several noncoding RNAs (ncRNAs), suggesting a role for these ncRNAs in RpoN-dependent phenotypes. We were also able to validate a number of transcriptional start sites, many of which were consistent with predicted promoter motifs. Overall, our approach provides an efficient way to survey global transcriptional activity in bacteria and enables rapid discovery of specific areas in the genome that merit further investigation.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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