Evidence map›Paper›PMID 21742981›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Quantifying the sequence-function relation in gene silencing by bacterial small RNAs.

Yue Hao, Zhongge J Zhang, David W Erickson, Min Huang, Yingwu Huang, Junbai Li, Terence Hwa, Hualin Shi

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.1field-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

34 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. What makes a small RNA work?Nucleic acids research · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Hfq chaperone brings speed dating to bacterial sRNA.Wiley interdisciplinary reviews. RNA · 2018
    Review
  11. Article
  12. RNA search engines empower the bacterial intranet.Biochemical Society transactions · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors at 5 institutions in 2 countries.

Yue HaoInstitute of Theoretical Physics and Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Zhongge J Zhang
David W Erickson
Min Huang
Yingwu Huang
Junbai Li
Terence Hwa
Hualin Shi
Institute of Theoretical Physics · CNCenter for Theoretical Biological Physics · USChinese Academy of Sciences · CNTsinghua University · CNUniversity of California, San Diego · US

Funding

MOLECULAR BIOPHYSICS TRAINING PROGRAMT32GM008326 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KOMIVES, ELIZABETH A. · 1989 to 2020
$7.5M
Quantitative Characterization & Modeling of sRNA-Mediated Gene RegulationR01GM077298 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HWA, TERENCE · 2007 to 2010
$1.3M
NIGMS NIH HHS R01 GM077298NIGMS NIH HHS R01-GM77298NIGMS NIH HHS T32 GM008326
6 · The paper itself

Abstract

Sequence-function relations for small RNA (sRNA)-mediated gene silencing were quantified for the sRNA RyhB and some of its mRNA targets in Escherichia coli. Numerous mutants of RyhB and its targets were generated and their in vivo functions characterized at various levels of target and RyhB expression. Although a core complementary region is required for repression by RyhB, variations in the complementary sequences of the core region gave rise to a continuum of repression strengths, correlated exponentially with the computed free energy of RyhB-target duplex formation. Moreover, sequence variations in the linker region known to interact with the RNA chaperone Hfq also gave rise to a continuum of repression strengths, correlated exponentially with the computed energy cost of keeping the linker region open. These results support the applicability of the thermodynamic model in predicting sRNA-mRNA interaction and suggest that sequences at these locations may be used to fine-tune the degree of repression. Surprisingly, a truncated RyhB without the Hfq-binding region is found to repress multiple targets of the wild-type RyhB effectively, both in the presence and absence of Hfq, even though the former is required for the activity of wild-type RyhB itself. These findings challenge the commonly accepted model concerning the function of Hfq in gene silencing-both in providing stability to the sRNAs and in catalyzing the target mRNAs to take on active conformations-and raise the intriguing question of why many endogenous sRNAs subject their functions to Hfq-dependences.

Indexed as

Genes, BacterialGene SilencingBacterial ProteinsBase SequenceBinding SitesEnergy MetabolismEscherichia coli K12Molecular Sequence DataMutagenesis, Site-DirectedNucleic Acid ConformationRNA, BacterialRNA Processing, Post-TranscriptionalRNA, UntranslatedSuperoxide DismutaseBacterial ProteinsRNA, BacterialRNA, UntranslatedSodB protein, BacteriaSuperoxide Dismutase

Identifiers

PMID21742981
PMCPMC3145688
OpenAlexW2052385345

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.