Evidence map›Paper›PMID 22492706›Full record

ArticleNucleic acids research2012

Extensive terminal and asymmetric processing of small RNAs from rRNAs, snoRNAs, snRNAs, and tRNAs.

Zhihua Li, Christine Ender, Gunter Meister, Patrick S Moore, Yuan Chang, Bino John

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 212 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 1% 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

212 citing papers in PubMed, 2 syntheses or guidelines pooled it, 366 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Unlocking the role of tRNA-derived fragments in shaping breast cancer signaling.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  10. Review
  11. Article
  12. Review
  13. The Roles of tRNA-Derived Fragments in Cancer: Updates and Perspectives.International journal of molecular sciences · 2025
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Overview of the Different Classes of Small RNAs During B-Cell Development.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  19. Review
  20. 5'-tRNANature communications · 2024
    Article

152 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 2 institutions in 2 countries.

Zhihua LiSchool of Medicine, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Christine Ender
Gunter Meister
Patrick S Moore
Yuan Chang
Bino John
University of Pittsburgh · USUPMC Hillman Cancer Center · US

Funding

Role of a New Polyomavirus in Merkel Cell CarcinomaR01CA136806 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MOORE, PATRICK S. · 2009 to 2015
$3.0M
Protein Biomarkers for a New Human Polyomavirus in AIDS-related MalignanciesR01CA136363 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MOORE, PATRICK S. · 2008 to 2015
$2.3M
Evolution, Biogenesis, and Function of microRNAsR01GM079756 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN, BINO · 2007 to 2011
$1.5M
NCI NIH HHS CA136363NCI NIH HHS CA136806NIGMS NIH HHS GM079756NIGMS NIH HHS R01 GM079756
6 · The paper itself

Abstract

Deep sequencing studies frequently identify small RNA fragments of abundant RNAs. These fragments are thought to represent degradation products of their precursors. Using sequencing, computational analysis, and sensitive northern blot assays, we show that constitutively expressed non-coding RNAs such as tRNAs, snoRNAs, rRNAs and snRNAs preferentially produce small 5' and 3' end fragments. Similar to that of microRNA processing, these terminal fragments are generated in an asymmetric manner that predominantly favors either the 5' or 3' end. Terminal-specific and asymmetric processing of these small RNAs occurs in both mouse and human cells. In addition to the known processing of some 3' terminal tRNA-derived fragments (tRFs) by the RNase III endonuclease Dicer, we show that several RNase family members can produce tRFs, including Angiogenin that cleaves the TψC loop to generate 3' tRFs. The 3' terminal tRFs but not the 5' tRFs are highly complementary to human endogenous retroviral sequences in the genome. Despite their independence from Dicer processing, these tRFs associate with Ago2 and are capable of down regulating target genes by transcript cleavage in vitro. We suggest that endogenous 3' tRFs have a role in regulating the unwarranted expression of endogenous viruses through the RNA interference pathway.

Indexed as

RNA Processing, Post-TranscriptionalAnimalsArgonaute ProteinsEndogenous RetrovirusesHumansMiceProteinsRibonuclease IIIRibonuclease, PancreaticRibonucleasesRNA-Binding ProteinsRNA CleavageRNA, MessengerRNA, RibosomalRNA, Small NuclearRNA, Small NucleolarAgo2 protein, mouseangiogeninArgonaute ProteinsDgcr8 protein, mouseProteinsRibonuclease IIIRibonuclease, PancreaticRibonucleasesRNA-Binding ProteinsRNA, MessengerRNA, RibosomalRNA, Small NuclearRNA, Small NucleolarRNA, Small UntranslatedRNA, Transfer

Identifiers

PMID22492706
PMCPMC3413118
OpenAlexW2151435150

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.