Evidence map›Paper›PMID 29893896›Full record

ArticleNucleic acids research2018

Dimerization confers increased stability to nucleases in 5' halves from glycine and glutamic acid tRNAs.

Juan Pablo Tosar, Fabiana Gámbaro, Leonardo Darré, Sergio Pantano, Eric Westhof, Alfonso Cayota

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  9. Emerging roles of transfer RNA fragments in the CNS.Brain : a journal of neurology · 2025
    Review
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  13. Article
  14. Diverse plant RNAs coatProceedings of the National Academy of Sciences of the United States of America · 2025
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  15. Article
  16. Roles and regulation of tRNA-derived small RNAs in animals.Nature reviews. Molecular cell biology · 2024
    Review
  17. Article
  18. Review
  19. Review
  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

6 authors at 3 institutions in 2 countries.

Juan Pablo TosarFunctional Genomics Unit, Institut Pasteur de Montevideo, Montevideo 11400, Uruguay.
Fabiana GámbaroFunctional Genomics Unit, Institut Pasteur de Montevideo, Montevideo 11400, Uruguay.
Leonardo DarréFunctional Genomics Unit, Institut Pasteur de Montevideo, Montevideo 11400, Uruguay.
Sergio PantanoGroup of Biomolecular Simulations, Institut Pasteur de Montevideo. Montevideo 11400, Uruguay.
Eric WesthofArchitecture et Réactivité de l'ARN, Université de Strasbourg, Institut de biologie moléculaire et cellulaire du CNRS, 15 rue René Descartes, 67084 Strasbourg, France.
Alfonso CayotaFunctional Genomics Unit, Institut Pasteur de Montevideo, Montevideo 11400, Uruguay.
Institut Pasteur de Montevideo · UYCentre National de la Recherche Scientifique · FRUniversidad de la República · UY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously shown that 5' halves from tRNAGlyGCC and tRNAGluCUC are the most enriched small RNAs in the extracellular space of human cell lines, and especially in the non-vesicular fraction. Extracellular RNAs are believed to require protection by either encapsulation in vesicles or ribonucleoprotein complex formation. However, deproteinization of non-vesicular tRNA halves does not affect their retention in size-exclusion chromatography. Thus, we considered alternative explanations for their extracellular stability. In-silico analysis of the sequence of these tRNA-derived fragments showed that tRNAGly 5' halves can form homodimers or heterodimers with tRNAGlu 5' halves. This capacity is virtually unique to glycine tRNAs. By analyzing synthetic oligonucleotides by size exclusion chromatography, we provide evidence that dimerization is possible in vitro. tRNA halves with single point substitutions preventing dimerization are degraded faster both in controlled nuclease digestion assays and after transfection in cells, showing that dimerization can stabilize tRNA halves against the action of cellular nucleases. Finally, we give evidence supporting dimerization of endogenous tRNAGlyGCC 5' halves inside cells. Considering recent reports have shown that 5' tRNA halves from Ala and Cys can form tetramers, our results highlight RNA intermolecular structures as a new layer of complexity in the biology of tRNA-derived fragments.

Indexed as

DimerizationRNA Stability5' Flanking RegionBase SequenceGlutamic AcidGlycineHumansMCF-7 CellsNucleic Acid ConformationRibonucleasesRNA, Transfer, GluRNA, Transfer, GlyGlutamic AcidGlycineRibonucleasesRNA, Transfer, GluRNA, Transfer, Gly

Identifiers

PMID29893896
PMCPMC6158491
OpenAlexW2808496870

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.