Evidence map›Paper›PMID 20052287›Full record

ArticlePLoS biology2010

Poised transcription factories prime silent uPA gene prior to activation.

Carmelo Ferrai, Sheila Q Xie, Paolo Luraghi, Davide Munari, Francisco Ramirez, Miguel R Branco, Ana Pombo, Massimo P Crippa

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 85 citations in OpenAlex.

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  7. Understanding 3D genome organization by multidisciplinary methods.Nature reviews. Molecular cell biology · 2021
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  9. Methods for mapping 3D chromosome architecture.Nature reviews. Genetics · 2020
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  15. Review
  16. Morphology of nuclear transcription.Histochemistry and cell biology · 2016
    Review
  17. Article
  18. Three-dimensional genome architecture: players and mechanisms.Nature reviews. Molecular cell biology · 2015
    Review
  19. Myosin VI regulates gene pairing and transcriptional pause release in T cells.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  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

8 authors at 3 institutions in 1 country.

Carmelo FerraiLaboratory of Molecular Dynamics of the Nucleus, Division of Genetics and Cell Biology, S Raffaele Scientific Institute, Milan, Italy.
Sheila Q Xie
Paolo Luraghi
Davide Munari
Francisco Ramirez
Miguel R Branco
Ana Pombo
Massimo P Crippa
Hammersmith Hospital · GBMedical Research Council · GBSouth West Thames Institute for Renal Research · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H008098/1Medical Research Council MC_U120061476
6 · The paper itself

Abstract

The position of genes in the interphase nucleus and their association with functional landmarks correlate with active and/or silent states of expression. Gene activation can induce chromatin looping from chromosome territories (CTs) and is thought to require de novo association with transcription factories. We identify two types of factory: "poised transcription factories," containing RNA polymerase II phosphorylated on Ser5, but not Ser2, residues, which differ from "active factories" associated with phosphorylation on both residues. Using the urokinase-type plasminogen activator (uPA) gene as a model system, we find that this inducible gene is predominantly associated with poised (S5p(+)S2p(-)) factories prior to activation and localized at the CT interior. Shortly after induction, the uPA locus is found associated with active (S5p(+)S2p(+)) factories and loops out from its CT. However, the levels of gene association with poised or active transcription factories, before and after activation, are independent of locus positioning relative to its CT. RNA-FISH analyses show that, after activation, the uPA gene is transcribed with the same frequency at each CT position. Unexpectedly, prior to activation, the uPA loci internal to the CT are seldom transcriptionally active, while the smaller number of uPA loci found outside their CT are transcribed as frequently as after induction. The association of inducible genes with poised transcription factories prior to activation is likely to contribute to the rapid and robust induction of gene expression in response to external stimuli, whereas gene positioning at the CT interior may be important to reinforce silencing mechanisms prior to induction.

Indexed as

AntibodiesChromatin Assembly and DisassemblyChromosomal Position EffectsGene Expression Regulation, EnzymologicGenesGene SilencingGenetic LociHep G2 CellsHumansMetalloendopeptidasesRNA Polymerase IITranscriptional ActivationUrokinase-Type Plasminogen ActivatorAntibodiesMBTPS2 protein, humanMetalloendopeptidasesRNA Polymerase IIUrokinase-Type Plasminogen Activator

Identifiers

PMID20052287
PMCPMC2797137
OpenAlexW2132283906

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.