Evidence map›Paper›PMID 29784889›Full record

ArticleThe Biochemical journal2018

SINHCAF/FAM60A and SIN3A specifically repress HIF-2α expression.

John Biddlestone, Michael Batie, Daniel Bandarra, Ivan Munoz, Sonia Rocha

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 13 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

5 authors at 3 institutions in 1 country.

John BiddlestoneCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Michael BatieCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Daniel BandarraCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Ivan MunozMRC Protein Phosphorylation Unit, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Sonia RochaCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K. srocha@liverpool.ac.uk.ORCID 0000-0002-2413-4981
University of Dundee · GBUniversity of Liverpool · GBMRC Protein Phosphorylation and Ubiquitylation Unit · GB

Funding

Cancer Research UK 12918Medical Research CouncilWellcome Trust 097945/B/11/ZWellcome Trust 206293/Z/17/Z
6 · The paper itself

Abstract

The SIN3A-HDAC (histone deacetylase) complex is a master transcriptional repressor, required for development but often deregulated in disease. Here, we report that the recently identified new component of this complex, SINHCAF (SIN3A and HDAC-associated factor)/FAM60A (family of homology 60A), links the SIN3A-HDAC co-repressor complex function to the hypoxia response. We show that SINHCAF specifically represses HIF-2α mRNA and protein expression, via its interaction with the transcription factor SP1 (specificity protein 1) and recruitment of HDAC1 to the HIF-2α promoter. SINHCAF control over HIF-2α results in functional cellular changes in

Indexed as

Gene Expression RegulationA549 CellsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsEndothelial PAS Domain-Containing Protein 1HeLa CellsHistone Deacetylase 1HumansPromoter Regions, GeneticRepressor ProteinsRNA, MessengerSin3 Histone Deacetylase and Corepressor ComplexBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsEndothelial PAS Domain-Containing Protein 1HDAC1 protein, humanHistone Deacetylase 1Repressor ProteinsRNA, MessengerSIN3A transcription factorSin3 Histone Deacetylase and Corepressor ComplexSINHCAF protein, humanHIF-2histone deacetylaseshypoxiahypoxia-inducible factorsSIN3ASP1transcription

Identifiers

PMID29784889
PMCPMC6024822
OpenAlexW2803170154

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.