Evidence map›Paper›PMID 22895111›Full record

ArticleCell cycle (Georgetown, Tex.)2012

Transcriptional targeting by microRNA-polycomb complexes: a novel route in cell fate determination.

Giuseppe Zardo, Alberto Ciolfi, Laura Vian, Monia Billi, Serena Racanicchi, Francesco Grignani, Clara Nervi

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 40 citations in OpenAlex.

  1. Nuclear miRNAs: Gene Regulation Activities.International journal of molecular sciences · 2024
    Review
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  10. Involvement of MicroRNA in T-Cell Differentiation and Malignancy.International journal of hematology-oncology and stem cell research · 2015
    Review
  11. Article
  12. Article
  13. Article
  14. MicroRNAs as novel regulators of stem cell fate.World journal of stem cells · 2013
    Review
  15. Article
  16. Article
  17. 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 3 institutions in 2 countries.

Giuseppe ZardoDepartment of Cellular Biotechnologies and Hematology, University La Sapienza, Rome, Italy.
Alberto Ciolfi
Laura Vian
Monia Billi
Serena Racanicchi
Francesco Grignani
Clara Nervi
Sapienza University of Rome · ITUniversity of Perugia · ITGeneral Department of Preventive Medicine · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in the understanding of the epigenetic events underlying the regulation of developmental genes expression and cell lineage commitment are revealing novel regulatory networks. These also involve distinct components of the epigenetic pathways, including chromatin histone modification, DNA methylation, repression by polycomb complexes and microRNAs. Changes in chromatin structure, DNA methylation status and microRNA expression levels represent flexible, reversible and heritable mechanisms for the maintenance of stem cell states and cell fate decisions. We recently provided novel evidence showing that microRNAs, besides determining the post-transcriptional gene silencing of their targets, also bind to evolutionarily conserved complementary genomic seed-matches present on target gene promoters. At these sites, microRNAs can function as a critical interface between chromatin remodeling complexes and the genome for transcriptional gene silencing. Here, we discuss our novel findings supporting a role of the transcriptional chromatin targeting by polycomb-microRNA complexes in lineage fate determination of human hematopoietic cells.

Indexed as

Transcription, GeneticBase SequenceCell LineageChromatinEpigenesis, GeneticEvolution, MolecularHematopoiesisHumansMicroRNAsModels, GeneticPolycomb-Group ProteinsPromoter Regions, GeneticChromatinMicroRNAsPolycomb-Group Proteins

Identifiers

PMID22895111
PMCPMC3478304
OpenAlexW1989829872

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.