Evidence map›Paper›PMID 26816005›Full record

ArticlePloS one2016

Homologous Transcription Factors DUX4 and DUX4c Associate with Cytoplasmic Proteins during Muscle Differentiation.

Eugénie Ansseau, Jocelyn O Eidahl, Céline Lancelot, Alexandra Tassin, Christel Matteotti, Cassandre Yip, Jian Liu, Baptiste Leroy, Céline Hubeau, Cécile Gerbaux and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Muscular Dystrophies.Advances in experimental medicine and biology · 2025
    Review
  4. Review
  5. Article
  6. Influence ofInternational journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. iScience · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. A Pediatric Review of Facioscapulohumeral Muscular Dystrophy.Journal of pediatric neurology : JPN · 2018
    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

20 authors at 4 institutions in 3 countries.

Eugénie AnsseauLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Jocelyn O EidahlCenter for Gene Therapy, Research Institute at Nationwide Children's Hospital, Columbus, OH, United States of America.
Céline LancelotLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Alexandra TassinLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Christel MatteottiLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Cassandre YipLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Jian LiuCenter for Gene Therapy, Research Institute at Nationwide Children's Hospital, Columbus, OH, United States of America.
Baptiste LeroyLaboratory of Proteomic and Microbiology, Research Institute for Biosciences, University of Mons, Mons, Belgium.
Céline HubeauLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Cécile GerbauxLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Samuel CloetLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Armelle WautersLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Sabrina ZorboLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Pierre MeyerPediatric Department, CHRU Montpellier, Montpellier, France.
Isabelle PirsonI.R.I.B.H.M., Free University of Brussels, Brussels, Belgium.
Dalila Laoudj-ChenivesseLaboratory of Physiology and Experimental Medicine, INSERM U1046, Montpellier, France.
Ruddy WattiezLaboratory of Proteomic and Microbiology, Research Institute for Biosciences, University of Mons, Mons, Belgium.
Scott Q HarperCenter for Gene Therapy, Research Institute at Nationwide Children's Hospital, Columbus, OH, United States of America.
Alexandra BelayewLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
Frédérique CoppéeLaboratory of Molecular Biology, Research Institute for Health Sciences and Technology, University of Mons, Mons, Belgium.
University of Mons · BENationwide Children's Hospital · USCentre Hospitalier Universitaire de Montpellier · FRInserm · FR

Funding

Myogenesis Studies for FSHD BiomarkersU54HD060848 · NICHD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI EMERSON, CHARLES P. · 2008 to 2017
$16.1M
The Ohio State University Center for Clinical and Translational Science (KL2)KL2RR025754 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$3.5M
DUX4 and the P53 pathway in FSHD pathogenesisR01AR062123 · NIAMS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI HARPER, SCOTT Q · 2012 to 2016
$1.6M
Structure/Function of N-ethylmaleimide Sensitive FactorR01NS046242 · NINDS · UNIVERSITY OF KENTUCKY · PI WHITEHEART, SIDNEY WALDO · 2004 to 2007
$1.1M
Training in neuromuscular diseasesT32NS077984 · NINDS · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C, MENDELL, JERRY ROY · 2012 to 2016
$946k
NCRR NIH HHS KL2 RR025754NCRR NIH HHS KL2RR025754NIAMS NIH HHS 5 R01 AR 062123 -03NIAMS NIH HHS R01 AR062123NICHD NIH HHS U54 HD060848NINDS NIH HHS 5T32NS077984-02NINDS NIH HHS NS046242NINDS NIH HHS R01 NS046242NINDS NIH HHS T32 NS077984
6 · The paper itself

Abstract

Hundreds of double homeobox (DUX) genes map within 3.3-kb repeated elements dispersed in the human genome and encode DNA-binding proteins. Among these, we identified DUX4, a potent transcription factor that causes facioscapulohumeral muscular dystrophy (FSHD). In the present study, we performed yeast two-hybrid screens and protein co-purifications with HaloTag-DUX fusions or GST-DUX4 pull-down to identify protein partners of DUX4, DUX4c (which is identical to DUX4 except for the end of the carboxyl terminal domain) and DUX1 (which is limited to the double homeodomain). Unexpectedly, we identified and validated (by co-immunoprecipitation, GST pull-down, co-immunofluorescence and in situ Proximal Ligation Assay) the interaction of DUX4, DUX4c and DUX1 with type III intermediate filament protein desmin in the cytoplasm and at the nuclear periphery. Desmin filaments link adjacent sarcomere at the Z-discs, connect them to sarcolemma proteins and interact with mitochondria. These intermediate filament also contact the nuclear lamina and contribute to positioning of the nuclei. Another Z-disc protein, LMCD1 that contains a LIM domain was also validated as a DUX4 partner. The functionality of DUX4 or DUX4c interactions with cytoplasmic proteins is underscored by the cytoplasmic detection of DUX4/DUX4c upon myoblast fusion. In addition, we identified and validated (by co-immunoprecipitation, co-immunofluorescence and in situ Proximal Ligation Assay) as DUX4/4c partners several RNA-binding proteins such as C1QBP, SRSF9, RBM3, FUS/TLS and SFPQ that are involved in mRNA splicing and translation. FUS and SFPQ are nuclear proteins, however their cytoplasmic translocation was reported in neuronal cells where they associated with ribonucleoparticles (RNPs). Several other validated or identified DUX4/DUX4c partners are also contained in mRNP granules, and the co-localizations with cytoplasmic DAPI-positive spots is in keeping with such an association. Large muscle RNPs were recently shown to exit the nucleus via a novel mechanism of nuclear envelope budding. Following DUX4 or DUX4c overexpression in muscle cell cultures, we observed their association with similar nuclear buds. In conclusion, our study demonstrated unexpected interactions of DUX4/4c with cytoplasmic proteins playing major roles during muscle differentiation. Further investigations are on-going to evaluate whether these interactions play roles during muscle regeneration as previously suggested for DUX4c.

Indexed as

Amino Acid SequenceAnimalsCell DifferentiationCell LineCytoplasmDesminHomeodomain ProteinsHumansKaryopherinsMiceMolecular Sequence DataMuscle DevelopmentMyoblastsProtein BindingRNA-Binding ProteinsSequence Homology, Amino AcidDesminDUX4L1 protein, humanDUX4L9 protein, humanHomeodomain ProteinsIPO13 protein, humanKaryopherinsRNA-Binding ProteinsTranscription Factors

Identifiers

PMID26816005
PMCPMC4729438
OpenAlexW2266398926

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.