Evidence map›Paper›PMID 28830349›Full record

ArticleBMC genomics2017

Prediction of bacterial small RNAs in the RsmA (CsrA) and ToxT pathways: a machine learning approach.

Carl Tony Fakhry, Prajna Kulkarni, Ping Chen, Rahul Kulkarni, Kourosh Zarringhalam

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Three Ribosomal Operons ofFrontiers in microbiology · 2021
    Article
  5. Binding ofFrontiers in microbiology · 2020
    Article
  6. Review
  7. 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

5 authors at 1 institution in 1 country.

Carl Tony FakhryDepartment of Computer Science, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, 02125, MA, USA.
Prajna KulkarniDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, 02125, MA, USA.
Ping ChenDepartment of Engineering, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, 02125, MA, USA.
Rahul KulkarniDepartment of Physics, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, 02125, MA, USA.
Kourosh ZarringhalamDepartment of Mathematics, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, 02125, MA, USA. kourosh.zarringhalam@umb.edu.
University of Massachusetts Boston · US

Funding

UMass Boston-DF/HCC U54 Partnership (2 of 2)U54CA156734 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI ADAN COLON-CARMONA, Jill A. Macoska · 2010 to 2026
$24.9M
NCI NIH HHS U54 CA156734
6 · The paper itself

Abstract

backgroundSmall RNAs (sRNAs) constitute an important class of post-transcriptional regulators that control critical cellular processes in bacteria. Recent research using high-throughput transcriptomic approaches has led to a dramatic increase in the discovery of bacterial sRNAs. However, it is generally believed that the currently identified sRNAs constitute a limited subset of the bacterial sRNA repertoire. In several cases, sRNAs belonging to a specific class are already known and the challenge is to identify additional sRNAs belonging to the same class. In such cases, machine-learning approaches can be used to predict novel sRNAs in a given class.

methodsIn this work, we develop novel bioinformatics approaches that integrate sequence and structure-based features to train machine-learning models for the discovery of bacterial sRNAs. We show that features derived from recurrent structural motifs in the ensemble of low energy secondary structures can distinguish the RNA classes with high accuracy.

resultsWe apply this approach to predict new members in two broad classes of bacterial small RNAs: 1) sRNAs that bind to the RNA-binding protein RsmA/CsrA in diverse bacterial species and 2) sRNAs regulated by the master regulator of virulence, ToxT, in Vibrio cholerae.

conclusionThe involvement of sRNAs in bacterial adaptation to changing environments is an increasingly recurring theme in current research in microbiology. It is likely that future research, combining experimental and computational approaches, will discover many more examples of sRNAs as components of critical regulatory pathways in bacteria. We have developed a novel approach for prediction of small RNA regulators in important bacterial pathways. This approach can be applied to specific classes of sRNAs for which several members have been identified and the challenge is to identify additional sRNAs.

Indexed as

Machine LearningBacterial ProteinsBase SequenceComputational BiologyRNA, BacterialVibrio choleraeBacterial ProteinsRNA, BacterialBacterial small RNABoltzmannCsrAMachine learningRNA structureRsmAToxT

Identifiers

PMID28830349
PMCPMC5568370
OpenAlexW2745345596

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.