Evidence map›Paper›PMID 20620951›Full record

ArticleMolecular cell2010

Diverse endonucleolytic cleavage sites in the mammalian transcriptome depend upon microRNAs, Drosha, and additional nucleases.

Fedor V Karginov, Sihem Cheloufi, Mark M W Chong, Alexander Stark, Andrew D Smith, Gregory J Hannon

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

128 citing papers in PubMed, 193 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. The structural basis for RNA slicing by human Argonaute2.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Control of RNA degradation in cell fate decision.Frontiers in cell and developmental biology · 2023
    Review
  16. RNA binding proteins in MLL-rearranged leukemia.Experimental hematology & oncology · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Article

68 more citing papers are in PubMed but not listed here.

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 4 institutions in 3 countries.

Fedor V KarginovWatson School of Biological Sciences, Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
Sihem Cheloufi
Mark M W Chong
Alexander Stark
Andrew D Smith
Gregory J Hannon
Howard Hughes Medical Institute · USResearch Institute of Molecular Pathology · ATUniversity of Southern California · USWalter and Eliza Hall Institute of Medical Research · AU

Funding

VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
MECHANISMS OF DSRNA-INDUCED GENE SILENCINGR01GM062534 · NIGMS · COLD SPRING HARBOR LABORATORY · PI HANNON, GREGORY J · 2000 to 2012
$4.3M
NCI NIH HHS P01 CA013106NIGMS NIH HHS R01 GM062534
6 · The paper itself

Abstract

The life span of a mammalian mRNA is determined, in part, by the binding of regulatory proteins and small RNA-guided complexes. The conserved endonuclease activity of Argonaute2 requires extensive complementarity between a small RNA and its target and is not used by animal microRNAs, which pair with their targets imperfectly. Here we investigate the endonucleolytic function of Ago2 and other nucleases by transcriptome-wide profiling of mRNA cleavage products retaining 5' phosphate groups in mouse embryonic stem cells (mESCs). We detect a prominent signature of Ago2-dependent cleavage events and validate several such targets. Unexpectedly, a broader class of Ago2-independent cleavage sites is also observed, indicating participation of additional nucleases in site-specific mRNA cleavage. Within this class, we identify a cohort of Drosha-dependent mRNA cleavage events that functionally regulate mRNA levels in mESCs, including one in the Dgcr8 mRNA. Together, these results highlight the underappreciated role of endonucleolytic cleavage in controlling mRNA fates in mammals.

Indexed as

AnimalsArgonaute ProteinsCell LineComputational BiologyEmbryonic Stem CellsEndoribonucleasesEukaryotic Initiation Factor-2Gene Expression ProfilingMiceMicroRNAsPhosphorylationProteinsRibonuclease IIIRNA-Binding ProteinsRNA, MessengerAgo2 protein, mouseArgonaute ProteinsDgcr8 protein, mouseDrosha protein, mouseEndoribonucleasesEukaryotic Initiation Factor-2MicroRNAsProteinsRibonuclease IIIRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID20620951
PMCPMC2914474
OpenAlexW2152267176

What OpenQuestion holds

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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.