Evidence map›Paper›PMID 35191484›Full record

ArticleBiology open2022

Downstream events initiated by expression of FSHD-associated DUX4: Studies of nucleocytoplasmic transport, γH2AX accumulation, and Bax/Bak-dependence.

Isabel F Masteika, Anvitha Sathya, Sachiko Homma, Bess M Miller, Frederick M Boyce, Jeffrey Boone Miller

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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 3 institutions in 1 country.

Isabel F MasteikaDepartment of Neurology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.ORCID 0000-0001-7607-1380
Anvitha SathyaDepartment of Neurology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.ORCID 0000-0001-8858-7851
Sachiko HommaDepartment of Neurology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.ORCID 0000-0001-6563-8521
Bess M MillerBiological & Biomedical Sciences Program, Harvard Medical School, Boston, Massachusetts 02115, USA.ORCID 0000-0002-9868-5436
Frederick M BoyceDepartment of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Jeffrey Boone MillerDepartment of Neurology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.ORCID 0000-0001-5273-2201
Boston University · USHarvard University · USMassachusetts General Hospital · US

Funding

Mechanisms of DUX4 mediated FSHD pathologyR01AR062587 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JONES, PETER L · 2013 to 2024
$5.3M
NIAMS NIH HHS R01 AR062587NIH HHS R01AR062587
6 · The paper itself

Abstract

Abnormal expression in skeletal muscle of the double homeobox transcription factor DUX4 underlies pathogenesis in facioscapulohumeral muscular dystrophy (FSHD). Though multiple changes are known to be initiated by aberrant DUX4 expression, the downstream events initiated by DUX4 remain incompletely understood. In this study, we examined plausible downstream events initiated by DUX4. First, we found that nucleocytoplasmic protein export appeared to be decreased upon DUX4 expression as indicated by nuclear accumulation of a shuttle-GFP reporter. Second, building on studies from other labs, we showed that phospho(Ser139)-H2AX (γH2AX), an indicator of double-strand DNA breaks, accumulated both in human FSHD1 myotube nuclei upon endogenous DUX4 expression and in Bax-/-;Bak-/- (double knockout), SV40-immortalized mouse embryonic fibroblasts upon exogenous DUX4 expression. In contrast, DUX4-induced caspase 3/7 activation was prevented in Bax-/-;Bak-/- double knockout SV40-MEFs, but not by single knockouts of Bax, Bak, or Bid. Thus, aberrant DUX4 expression appeared to alter nucleocytoplasmic protein transport and generate double-strand DNA breaks in FSHD1 myotube nuclei, and the Bax/Bak pathway is required for DUX4-induced caspase activation but not γH2AX accumulation. These results add to our knowledge of downstream events induced by aberrant DUX4 expression and suggest possibilities for further mechanistic investigation.

Indexed as

bcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer ProteinHistonesHomeodomain ProteinsMuscular Dystrophy, FacioscapulohumeralActive Transport, Cell NucleusAnimalsFibroblastsMiceBak1 protein, mouseBax protein, mousebcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer ProteinDux4 protein, mousegamma-H2AX protein, mouseHistonesHomeodomain ProteinsBAXDUX4Facioscapulohumeral muscular dystrophyMyotubePhospho(Ser139)-H2AXγH2AX

Identifiers

PMID35191484
PMCPMC8890089
OpenAlexW4213369041

What OpenQuestion holds

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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.