Evidence map›Paper›PMID 24723422›Full record

ArticleMolecular biology and evolution2014

Inferring the evolutionary history of primate microRNA binding sites: overcoming motif counting biases.

Alfred T Simkin, Jeffrey A Bailey, Fen-Biao Gao, Jeffrey D Jensen

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  8. Inferring the demographic history of aye-ayes (bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Evolutionary Transitions of MicroRNA-Target Pairs.Genome biology and evolution · 2016
    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

4 authors at 2 institutions in 2 countries.

Alfred T SimkinProgram in Bioinformatics & Integrative Biology, University of Massachusetts Medical SchoolDepartment of Neurology, University of Massachusetts Medical SchoolSwiss Institute of Bioinformatics (SIB), Lausanne, Switzerland alfred.simkin@umassmed.edu.
Jeffrey A BaileyProgram in Bioinformatics & Integrative Biology, University of Massachusetts Medical School.
Fen-Biao GaoDepartment of Neurology, University of Massachusetts Medical School.
Jeffrey D JensenSwiss Institute of Bioinformatics (SIB), Lausanne, SwitzerlandEcole Polytechnique Federale de Lausanne (EPFL), School of Life Sciences, Lausanne, Switzerland.
University of Massachusetts Chan Medical School · USSIB Swiss Institute of Bioinformatics · CH

Funding

The MicroRNA Pathway in Translational Regulation of Neuronal DevelopmentR01NS066586 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GAO, FEN-BIAO · 2009 to 2013
$1.9M
Interactions between TDP-43 and microRNA-92 in Drosophila and human neuronsR21NS086318 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GAO, FEN-BIAO · 2014 to 2015
$461k
NINDS NIH HHS R01 NS066586NINDS NIH HHS R01NS066586NINDS NIH HHS R21 NS086318
6 · The paper itself

Abstract

The first microRNAs (miRNAs) were identified as essential, conserved regulators of gene expression, targeting the same genes across nearly all bilaterians. However, there are also prominent examples of conserved miRNAs whose functions appear to have shifted dramatically, sometimes over very brief periods of evolutionary time. To determine whether the functions of conserved miRNAs are stable or dynamic over evolutionary time scales, we have here defined the neutral turnover rates of short sequence motifs in predicted primate 3'-UTRs. We find that commonly used approaches to quantify motif turnover rates, which use a presence/absence scoring in extant lineages to infer ancestral states, are inherently biased to infer the accumulation of new motifs, leading to the false inference of continually increasing regulatory complexity over time. Using a maximum likelihood approach to reconstruct individual ancestral nucleotides, we observe that binding sites of conserved miRNAs in fact have roughly equal numbers of gain and loss events relative to ancestral states and turnover extremely slowly relative to nearly identical permutations of the same motif. Contrary to case studies showing examples of functional turnover, our systematic study of miRNA binding sites suggests that in primates, the regulatory roles of conserved miRNAs are strongly conserved. Our revised methodology may be used to quantify the mechanism by which regulatory networks evolve.

Indexed as

3' Untranslated RegionsAnimalsBase SequenceBinding SitesConserved SequenceEvolution, MolecularHumansLikelihood FunctionsMicroRNAsPhylogenyPrimatesSelection, Genetic3' Untranslated RegionsMicroRNAsmiRNA evolutionmolecular evolutionmolecular phylogenymotif turnoverparsimonyregulatory network

Identifiers

PMID24723422
PMCPMC4069616
OpenAlexW2171456746

What OpenQuestion holds

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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.