Evidence map›Paper›PMID 27519343›Full record

ArticleBMC genomics2016

Genome-wide identification of transcriptional start sites in the haloarchaeon Haloferax volcanii based on differential RNA-Seq (dRNA-Seq).

Julia Babski, Karina A Haas, Daniela Näther-Schindler, Friedhelm Pfeiffer, Konrad U Förstner, Matthias Hammelmann, Rolf Hilker, Anke Becker, Cynthia M Sharma, Anita Marchfelder and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 154 citations in OpenAlex.

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  5. Archaeal RNA processing and regulation: expanding the functional landscape.Microbiology and molecular biology reviews : MMBR · 2025
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  10. Journal of bacteriology · 2025
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  11. Chromatin and gene regulation in archaea.Molecular microbiology · 2025
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  14. Studying the long-term adaptation ofFrontiers in microbiology · 2025
    Article
  15. MinD2 modulates cell shape and motility in the archaeonbioRxiv : the preprint server for biology · 2024
    Article
  16. Article
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  18. Article
  19. MinD proteins regulate CetZ1 localization inFrontiers in microbiology · 2024
    Article
  20. Article

28 more citing papers are in PubMed but not listed here.

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 6 institutions in 1 country.

Julia BabskiInstitute for Molecular Biosciences, Goethe University, Biocentre, Max-von-Laue-Str. 9, D-60439, Frankfurt, Germany.
Karina A HaasBiologie II, University of Ulm, 89069, Ulm, Germany.
Daniela Näther-SchindlerInstitute for Molecular Biosciences, Goethe University, Biocentre, Max-von-Laue-Str. 9, D-60439, Frankfurt, Germany.
Friedhelm PfeifferComputational Biology Group, MaxPlanckInstitute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.
Konrad U FörstnerResearch Center for Infectious Diseases (ZINF), University of Würzburg, Josef-Schneider-Str. 2/D15, 97080, Würzburg, Germany.
Matthias HammelmannInstitute for Molecular Biosciences, Goethe University, Biocentre, Max-von-Laue-Str. 9, D-60439, Frankfurt, Germany.
Rolf HilkerBioinformatik und Systembiologie, University of Gießen, Heinrich-Buff-Ring 58, 35392, Gießen, Germany.
Anke BeckerLOEWE-Center for Synthetic Microbiology, Hans-Meerwein-Str., 35032, Marburg, Germany.
Cynthia M SharmaResearch Center for Infectious Diseases (ZINF), University of Würzburg, Josef-Schneider-Str. 2/D15, 97080, Würzburg, Germany.
Anita MarchfelderBiologie II, University of Ulm, 89069, Ulm, Germany. anita.marchfelder@uni-ulm.de.
Jörg SoppaInstitute for Molecular Biosciences, Goethe University, Biocentre, Max-von-Laue-Str. 9, D-60439, Frankfurt, Germany. soppa@bio.uni-frankfurt.de.
Goethe University Frankfurt · DEUniversität Ulm · DEUniversity of Würzburg · DELoewe Center for Synthetic Microbiology · DEMax Planck Institute of Biochemistry · DEUniversity of Giessen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDifferential RNA-Seq (dRNA-Seq) is a recently developed method of performing primary transcriptome analyses that allows for the genome-wide mapping of transcriptional start sites (TSSs) and the identification of novel transcripts. Although the transcriptomes of diverse bacterial species have been characterized by dRNA-Seq, the transcriptome analysis of archaeal species is still rather limited. Therefore, we used dRNA-Seq to characterize the primary transcriptome of the model archaeon Haloferax volcanii.

resultsThree independent cultures of Hfx. volcanii grown under optimal conditions to the mid-exponential growth phase were used to determine the primary transcriptome and map the 5'-ends of the transcripts. In total, 4749 potential TSSs were detected. A position weight matrix (PWM) was derived for the promoter predictions, and the results showed that 64 % of the TSSs were preceded by stringent or relaxed basal promoters. Of the identified TSSs, 1851 belonged to protein-coding genes. Thus, fewer than half (46 %) of the 4040 protein-coding genes were expressed under optimal growth conditions. Seventy-two percent of all protein-coding transcripts were leaderless, which emphasized that this pathway is the major pathway for translation initiation in haloarchaea. A total of 2898 of the TSSs belonged to potential non-coding RNAs, which accounted for an unexpectedly high fraction (61 %) of all transcripts. Most of the non-coding TSSs had not been previously described (2792) and represented novel sequences (59 % of all TSSs). A large fraction of the potential novel non-coding transcripts were cis-antisense RNAs (1244 aTSSs). A strong negative correlation between the levels of antisense transcripts and cognate sense mRNAs was found, which suggested that the negative regulation of gene expression via antisense RNAs may play an important role in haloarchaea. The other types of novel non-coding transcripts corresponded to internal transcripts overlapping with mRNAs (1153 iTSSs) and intergenic small RNA (sRNA) candidates (395 TSSs).

conclusionThis study provides a comprehensive map of the primary transcriptome of Hfx. volcanii grown under optimal conditions. Fewer than half of all protein-coding genes have been transcribed under these conditions. Unexpectedly, more than half of the detected TSSs belonged to several classes of non-coding RNAs. Thus, RNA-based regulation appears to play a more important role in haloarchaea than previously anticipated.

Indexed as

Genome, Archaeal5' Untranslated RegionsGene LibraryHaloferax volcaniiHigh-Throughput Nucleotide SequencingOpen Reading FramesPromoter Regions, GeneticRNA, AntisenseRNA, ArchaealRNA, UntranslatedSequence Analysis, RNATranscription Initiation SiteTranscriptome5' Untranslated RegionsRNA, AntisenseRNA, ArchaealRNA, UntranslatedAntisense RNAArchaeadRNA-SeqHaloferax volcaniiLeaderless transcriptNon-coding RNAPromotersRNATranscriptome

Identifiers

PMID27519343
PMCPMC4983044
OpenAlexW2513021116

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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.