Evidence map›Paper›PMID 26137849›Full record

ArticleRNA (New York, N.Y.)2015

Divergent target recognition by coexpressed 5'-isomiRs of miR-142-3p and selective viral mimicry.

Mark Manzano, Eleonora Forte, Archana N Raja, Matthew J Schipma, Eva Gottwein

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Identification of a conserved RNA structure in thebioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Viral miRNA regulation of host gene expression.Seminars in cell & developmental biology · 2023
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Epitranscriptomics of cardiovascular diseases (Review).International journal of molecular medicine · 2022
    Review
  14. Article
  15. Article
  16. Review
  17. Mir142 loss unlocks IDH2Scientific reports · 2020
    Article
  18. Article
  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

5 authors.

Mark ManzanoDepartment of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Eleonora ForteDepartment of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Archana N RajaDepartment of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Matthew J SchipmaCenter for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Eva GottweinDepartment of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.

Funding

Kaposi's Sarcoma-associated Herpesvirus Mimics of Cellular microRNAsR01CA180813 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOTTWEIN, EVA HENRIETTE · 2014 to 2018
$1.6M
NCI NIH HHS R01 CA180813
6 · The paper itself

Abstract

Sequence heterogeneity at the ends of mature microRNAs (miRNAs) is well documented, but its effects on miRNA function are largely unexplored. Here we studied the impact of miRNA 5'-heterogeneity, which affects the seed region critical for target recognition. Using the example of miR-142-3p, an emerging regulator of the hematopoietic lineage in vertebrates, we show that naturally coexpressed 5'-variants (5'-isomiRs) can recognize largely distinct sets of binding sites. Despite this, both miR-142-3p isomiRs regulate exclusive and shared targets involved in actin dynamics. Thus, 5'-heterogeneity can substantially broaden and enhance regulation of one pathway. Other 5'-isomiRs, in contrast, recognize largely overlapping sets of binding sites. This is exemplified by two herpesviral 5'-isomiRs that selectively mimic one of the miR-142-3p 5'-isomiRs. We hypothesize that other cellular and viral 5'-isomiRs can similarly be grouped into those with divergent or convergent target repertoires, based on 5'-sequence features. Taken together, our results provide a detailed characterization of target recognition by miR-142-3p and its 5'-isomiR-specific viral mimic. We furthermore demonstrate that miRNA 5'-end variation leads to differential targeting and can thus broaden the target range of miRNAs.

Indexed as

ActinsAnimalsBinding SitesCell LineFemaleGenetic HeterogeneityHEK293 CellsHerpesvirus 8, HumanHumansMaleMicroRNAsMolecular MimicryMolecular Sequence DataRNA, ViralSequence Analysis, RNASpecies SpecificityActinsMicroRNAsRNA, ViralisomiRKaposi's sarcoma associated herpesvirusmiR-142-3pmiR-K10amiRNA

Identifiers

PMID26137849
PMCPMC4536321

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Registered trials

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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.