Evidence map›Paper›PMID 20865272›Full record

ArticleHistochemistry and cell biology2010

DNA binding sites target nuclear NFATc1 to heterochromatin regions in adult skeletal muscle fibers.

Tiansheng Shen, Yewei Liu, Minerva Contreras, Erick O Hernández-Ochoa, William R Randall, Martin F Schneider

Open access · greenAbstract read
In one paragraph

Article in Histochemistry and cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Voltage sensor movements of CaProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. How Postural Muscle Senses Disuse? Early Signs and Signals.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Histochemistry and cell biology: the annual review 2010.Histochemistry and cell biology · 2011
    Review
  13. Regulation of nucleocytoplasmic transport in skeletal muscle.Current topics in developmental biology · 2011
    Review
  14. 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

6 authors at 1 institution in 1 country.

Tiansheng ShenDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Baltimore, MD 21201-1503, USA.
Yewei Liu
Minerva Contreras
Erick O Hernández-Ochoa
William R Randall
Martin F Schneider
University of Maryland, Baltimore · US

Funding

Activity Dependent Signaling in Adult Skeletal Muscle Fiber PlasticityR01AR056477 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHNEIDER, MARTIN F · 2008 to 2012
$1.6M
NIAMS NIH HHS R01 AR056477NIAMS NIH HHS R01-AR056477
6 · The paper itself

Abstract

We have previously demonstrated that Ca²+/calcineurin-dependent dephosphorylation of the transcription factor nuclear factor of activated T cells subtype 1 (NFATc1) during repetitive skeletal muscle activity causes NFAT nuclear translocation and concentration in subnuclear NFAT foci. We now show that NFAT nuclear foci colocalize with heterochromatin regions of intense staining by DAPI or TO-PRO-3 that are present in the nucleus prior to NFATc1 nuclear entry. Nuclear NFATc1 also colocalizes with the heterochromatin markers trimethyl-histone H3 (Lys9) and heterochromatin protein 1α. Mutation of the NFATc1 DNA binding sites prevents entry and localization of NFATc1 in heterochromatin regions. However, fluorescence in situ hybridization shows that the NFAT-regulated genes for slow and fast myosin heavy chains are not localized within the heterochromatin regions. Fluorescence recovery after photobleaching shows that within a given nucleus, NFATc1 redistributes relatively rapidly (t(¹/₂) < 1 min) between NFAT foci. Nuclear export of an NFATc1 mutant not concentrated in NFAT foci is accelerated following nuclear entry during fiber activity, indicating buffering of free nuclear NFATc1 by NFATc1 within the NFAT foci. Taken together, our results suggest that NFAT foci serve as nuclear storage sites for NFATc1, allowing it to rapidly mobilize to other nuclear regions as required.

Indexed as

AdultAnimalsBinding SitesCell NucleusChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDNADNA-Binding ProteinsHeterochromatinHumansIn Situ Hybridization, FluorescenceMiceMuscle Fibers, SkeletalMuscle, SkeletalMutationNFATC Transcription FactorsChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDNADNA-Binding ProteinsHeterochromatinNFATC1 protein, humanNFATC Transcription FactorsNuclear ProteinsTranscription Factors

Identifiers

PMID20865272
PMCPMC3062432
OpenAlexW2015242941

What OpenQuestion holds

Textmetadata
LicenceTDM
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.