Evidence map›Paper›PMID 26779400›Full record

ArticleTranslation (Austin, Tex.)2014

AURA 2: Empowering discovery of post-transcriptional networks.

Erik Dassi, Angela Re, Sara Leo, Toma Tebaldi, Luigi Pasini, Daniele Peroni, Alessandro Quattrone

Open access · bronzeAbstract read
In one paragraph

Article in Translation (Austin, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. HuR controls glutaminase RNA metabolism.Nature communications · 2024
    Article
  6. Article
  7. Article
  8. RNA localization during early development of the axolotl.Frontiers in cell and developmental biology · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Genes · 2021
    Article
  15. Article
  16. The NMD Pathway RegulatesBiomedicines · 2021
    Article
  17. Article
  18. Article
  19. The eukaryotic translation initiation factor eIF4E elevates steady-state mProceedings of the National Academy of Sciences of the United States of America · 2020
    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

7 authors at 2 institutions in 2 countries.

Erik DassiLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Angela ReLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Sara LeoLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Toma TebaldiLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Luigi PasiniLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Daniele PeroniLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
Alessandro QuattroneLaboratory of Translational Genomics; Centre for Integrative Biology; University of Trento; Trento, Italy.
University of Trento · ITGenomics (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-transcriptional regulation (PTR) of gene expression is now recognized as a major determinant of cell phenotypes. The recent availability of methods to map protein-RNA interactions in entire transcriptomes such as RIP, CLIP and their variants, together with global polysomal and ribosome profiling techniques, are driving the exponential accumulation of vast amounts of data on mRNA contacts in cells, and of corresponding predictions of PTR events. However, this exceptional quantity of information cannot be exploited at its best to reconstruct potential PTR networks, as it still lies scattered throughout several databases and in isolated reports of single interactions. To address this issue, we developed the second and vastly enhanced version of the Atlas of UTR Regulatory Activity (AURA 2), a meta-database centered on mapping interaction of trans-factors with human and mouse UTRs. AURA 2 includes experimentally demonstrated binding sites for RBPs, ncRNAs, thousands of cis-elements, variations, RNA epigenetics data and more. Its user-friendly interface offers various data-mining features including co-regulation search, network generation and regulatory enrichment testing. Gene expression profiles for many tissues and cell lines can be also combined with these analyses to display only the interactions possible in the system under study. AURA 2 aims at becoming a valuable toolbox for PTR studies and at tracing the road for how PTR network-building tools should be designed. AURA 2 is available at http://aura.science.unitn.it.

Indexed as

cis-elementCLIPdatabasenon-coding RNApost-transcriptional regulationregulatory networkRNA-binding proteinRNA modificationtranslatomeUTR

Identifiers

PMID26779400
PMCPMC4705823
OpenAlexW2323943568

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.