Evidence map›Paper›PMID 21203457›Full record

ArticlePloS one2010

Tiling array analysis of UV treated Escherichia coli predicts novel differentially expressed small peptides.

Gard O S Thomassen, Ragnhild Weel-Sneve, Alexander D Rowe, James A Booth, Jessica M Lindvall, Karin Lagesen, Knut I Kristiansen, Magnar Bjørås, Torbjørn Rognes

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In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
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7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Gard O S ThomassenCentre for Molecular Biology and Neuroscience (CMBN) and Department of Microbiology, Rikshospitalet, Oslo University Hospital, Oslo, Norway.
Ragnhild Weel-Sneve
Alexander D Rowe
James A Booth
Jessica M Lindvall
Karin Lagesen
Knut I Kristiansen
Magnar Bjørås
Torbjørn Rognes

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite comprehensive investigation, the Escherichia coli SOS response system is not yet fully understood. We have applied custom designed whole genome tiling arrays to measure UV invoked transcriptional changes in E. coli. This study provides a more complete insight into the transcriptome and the UV irradiation response of this microorganism.

resultsWe detected a number of novel differentially expressed transcripts in addition to the expected SOS response genes (such as sulA, recN, uvrA, lexA, umuC and umuD) in the UV treated cells. Several of the differentially expressed transcripts might play important roles in regulation of the cellular response to UV damage. We have predicted 23 novel small peptides from our set of detected non-gene transcripts. Further, three of the predicted peptides were cloned into protein expression vectors to test the biological activity. All three constructs expressed the predicted peptides, in which two of them were highly toxic to the cell. Additionally, a remarkably high overlap with previously in-silico predicted non-coding RNAs (ncRNAs) was detected. Generally we detected a far higher transcriptional activity than the annotation suggests, and these findings correspond with previous transcription mappings from E. coli and other organisms.

conclusionsHere we demonstrate that the E. coli transcriptome consists of far more transcripts than the present annotation suggests, of which many transcripts seem important to the bacterial stress response. Sequence alignment of promoter regions suggest novel regulatory consensus sequences for some of the upregulated genes. Finally, several of the novel transcripts identified in this study encode putative small peptides, which are biologically active.

Indexed as

Gene Expression RegulationBase SequenceEscherichia coliMolecular Sequence DataOligonucleotide Array Sequence AnalysisOpen Reading FramesPeptidesPromoter Regions, GeneticReverse Transcriptase Polymerase Chain ReactionRNA, MessengerRNA, UntranslatedSOS Response, GeneticsTranscription, GeneticUltraviolet RaysPeptidesRNA, MessengerRNA, Untranslated

Identifiers

PMID21203457
PMCPMC3009722

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.