Evidence map›Paper›PMID 29905843›Full record

ArticleNucleic acids research2018

sRNA-dependent control of curli biosynthesis in Escherichia coli: McaS directs endonucleolytic cleavage of csgD mRNA.

Patrick Rosendahl Andreassen, Jens Sivkær Pettersen, Mateusz Szczerba, Poul Valentin-Hansen, Jakob Møller-Jensen, Mikkel Girke Jørgensen

Abstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Advances in sRNA-mediated regulation ofFrontiers in cellular and infection microbiology · 2025
    Review
  6. Article
  7. Small RNA OxyS induces resistance to aminoglycosides during oxidative stress by controlling Fe-S cluster biogenesis inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. CsrA Shows Selective Regulation of sRNA-mRNA Networks.bioRxiv : the preprint server for biology · 2023
    Article
  10. CsrA selectively modulates sRNA-mRNA regulator outcomes.Frontiers in molecular biosciences · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. CRISPRiFrontiers in nutrition · 2022
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
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

6 authors.

Patrick Rosendahl AndreassenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark. Campusvej 55, 5230 Odense M. Denmark.
Jens Sivkær PettersenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark. Campusvej 55, 5230 Odense M. Denmark.
Mateusz SzczerbaIra A. Fulton Schools of Engineering and School of Life Sciences, Arizona State University, Tempe, AZ, USA.
Poul Valentin-HansenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark. Campusvej 55, 5230 Odense M. Denmark.
Jakob Møller-JensenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark. Campusvej 55, 5230 Odense M. Denmark.
Mikkel Girke JørgensenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark. Campusvej 55, 5230 Odense M. Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Production of curli, extracellular protein structures important for Escherichia coli biofilm formation, is governed by a highly complex regulatory mechanism that integrates multiple environmental signals through the involvement of numerous proteins and small non-coding RNAs (sRNAs). No less than seven sRNAs (McaS, RprA, GcvB, RydC, RybB, OmrA and OmrB) are known to repress the expression of the curli activator CsgD. Many of the sRNAs repress CsgD production by binding to the csgD mRNA at sites far upstream of the ribosomal binding site. The precise mechanism behind sRNA-mediated regulation of CsgD synthesis is largely unknown. In this study, we identify a conserved A/U-rich region in the csgD mRNA 5' untranslated region, which is cleaved upon binding of the small RNAs, McaS, RprA or GcvB, to sites located more than 30 nucleotides downstream. Mutational analysis shows that the A/U-rich region as well as an adjacent stem-loop structure are required for McaS-stimulated degradation, also serving as a binding platform for the RNA chaperone Hfq. Prevention of McaS-activated cleavage completely relieves repression, suggesting that endoribonucleolytic cleavage of csgD mRNA is the primary regulatory effect exerted by McaS. Moreover, we find that McaS-mediated degradation of the csgD 5' untranslated region requires RNase E.

Indexed as

5' Untranslated RegionsBinding SitesEndoribonucleasesEscherichia coliEscherichia coli ProteinsHost Factor 1 ProteinNucleic Acid ConformationRNA CleavageRNA, MessengerRNA, Small UntranslatedTrans-Activators5' Untranslated RegionsCsgD protein, E coliEndoribonucleasesEscherichia coli ProteinsHfq protein, E coliHost Factor 1 Proteinribonuclease ERNA, MessengerRNA, Small UntranslatedTrans-Activators

Identifiers

PMID29905843
PMCPMC6061853

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.