Evidence map›Paper›PMID 25262352›Full record

ArticleNucleic acids research2014

Large-scale mapping of sequence-function relations in small regulatory RNAs reveals plasticity and modularity.

Neil Peterman, Anat Lavi-Itzkovitz, Erel Levine

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Distribution of prophage-encoded Pas sRNAs across pathogenicbioRxiv : the preprint server for biology · 2026
    Article
  2. What makes a small RNA work?Nucleic acids research · 2025
    Review
  3. Article
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  8. Design and Analysis of Massively Parallel Reporter Assays Using FORECAST.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
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  12. Review
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  14. Article
  15. Article
  16. Article
  17. Towards the complete small RNome ofMicrobial genomics · 2016
    Article
  18. Comprehensive analysis reveals how single nucleotides contribute to noncoding RNA function in bacterial quorum sensing.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  19. Article
  20. How do base-pairing small RNAs evolve?FEMS microbiology reviews · 2015
    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

3 authors at 2 institutions in 1 country.

Neil PetermanDepartment of Physics and FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA.
Anat Lavi-ItzkovitzDepartment of Physics and FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA.
Erel LevineDepartment of Physics and FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA elevine@fas.harvard.edu.
Center for Systems Biology · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two decades into the genomics era the question of mapping sequence to function has evolved from identifying functional elements to characterizing their quantitative properties including, in particular, their specificity and efficiency. Here, we use a large-scale approach to establish a quantitative map between the sequence of a bacterial regulatory RNA and its efficiency in modulating the expression of its targets. Our approach generalizes the sort-seq method, introduced recently to analyze promoter sequences, in order to accurately quantify the efficiency of a large library of sequence variants. We focus on two small RNAs (sRNAs) in E. coli, DsrA and RyhB, and their regulation of both repressed and activated targets. In addition to precisely identifying functional elements in the sRNAs, our data establish quantitative relationships between structural and energetic features of the sRNAs and their regulatory activity, and characterize a large set of direct and indirect interactions between nucleotides. A core of these interactions supports a model where specificity can be enhanced by a rigid molecular structure. Both sRNAs exhibit a modular design with limited cross-interactions, dividing the requirements for structural stability and target binding among modules.

Indexed as

Flow CytometryModels, BiologicalMutationNucleic Acid ConformationRNA, Small UntranslatedSequence Analysis, RNADsrA RNA, E coliRNA, Small Untranslated

Identifiers

PMID25262352
PMCPMC4231740
OpenAlexW2144527178

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.