Evidence map›Paper›PMID 26024923›Full record

ArticleBMC genomics2015

Single nucleotide resolution RNA-seq uncovers new regulatory mechanisms in the opportunistic pathogen Streptococcus agalactiae.

Isabelle Rosinski-Chupin, Elisabeth Sauvage, Odile Sismeiro, Adrien Villain, Violette Da Cunha, Marie-Elise Caliot, Marie-Agnès Dillies, Patrick Trieu-Cuot, Philippe Bouloc, Marie-Frédérique Lartigue and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
7.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 52 citations in OpenAlex.

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  13. Systematic dissection of σCell reports · 2021
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  17. Genetics of Lactococci.Microbiology spectrum · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Isabelle Rosinski-ChupinInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. ichupin@pasteur.fr.
Elisabeth SauvageInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. esauvage@pasteur.fr.
Odile SismeiroInstitut Pasteur, Transcriptome and Epigenome Platform, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. osisme@pasteur.fr.
Adrien VillainInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. avillain@pasteur.fr.
Violette Da CunhaInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. violette.da-cunha@pasteur.fr.
Marie-Elise CaliotInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. marie-elise.caliot@pasteur.fr.
Marie-Agnès DilliesInstitut Pasteur, Transcriptome and Epigenome Platform, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. marie-agnes.dillies@pasteur.fr.
Patrick Trieu-CuotInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. patrick.trieu-cuot@pasteur.fr.
Philippe BoulocInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, bâtiment 400, 91405, Orsay, France. philippe.bouloc@u-psud.fr.
Marie-Frédérique LartigueInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, bâtiment 400, 91405, Orsay, France. marie-frederique.lartigue@univ-tours.fr.
Philippe GlaserInstitut Pasteur, Unité de Biologie des Bactéries Pathogènes à Gram Positif, 28 rue du Docteur Roux, 75724,, Paris Cedex 15, France. philippe.glaser@pasteur.fr.
Institut Pasteur · FRCentre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStreptococcus agalactiae, or Group B Streptococcus, is a leading cause of neonatal infections and an increasing cause of infections in adults with underlying diseases. In an effort to reconstruct the transcriptional networks involved in S. agalactiae physiology and pathogenesis, we performed an extensive and robust characterization of its transcriptome through a combination of differential RNA-sequencing in eight different growth conditions or genetic backgrounds and strand-specific RNA-sequencing.

resultsOur study identified 1,210 transcription start sites (TSSs) and 655 transcript ends as well as 39 riboswitches and cis-regulatory regions, 39 cis-antisense non-coding RNAs and 47 small RNAs potentially acting in trans. Among these putative regulatory RNAs, ten were differentially expressed in response to an acid stress and two riboswitches sensed directly or indirectly the pH modification. Strikingly, 15% of the TSSs identified were associated with the incorporation of pseudo-templated nucleotides, showing that reiterative transcription is a pervasive process in S. agalactiae. In particular, 40% of the TSSs upstream genes involved in nucleotide metabolism show reiterative transcription potentially regulating gene expression, as exemplified for pyrG and thyA encoding the CTP synthase and the thymidylate synthase respectively.

conclusionsThis comprehensive map of the transcriptome at the single nucleotide resolution led to the discovery of new regulatory mechanisms in S. agalactiae. It also provides the basis for in depth analyses of transcriptional networks in S. agalactiae and of the regulatory role of reiterative transcription following variations of intra-cellular nucleotide pools.

Indexed as

Gene Expression ProfilingGene Expression Regulation, BacterialGene Regulatory NetworksGenes, BacterialHigh-Throughput Nucleotide SequencingNucleotidesRNA, BacterialRNA, MessengerSequence Analysis, RNAStreptococcus agalactiaeNucleotidesRNA, BacterialRNA, Messenger

Identifiers

PMID26024923
PMCPMC4448216
OpenAlexW1855672754

What OpenQuestion holds

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Registered trials

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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.