Evidence map›Paper›PMID 34266955›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Cholesterol is required for transcriptional repression by BASP1.

Amy E Loats, Samantha Carrera, Anna F Fleming, Abigail R E Roberts, Alice Sherrard, Eneda Toska, Alexander J Moorhouse, Kathryn F Medler, Stefan G E Roberts

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. 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
1.7field-weighted citation impact, top 15% 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, 27 citations in OpenAlex.

  1. Article
  2. Reactivation of the silencedProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Journal of medicinal chemistry · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Lipids and genes: Regulatory roles of lipids in RNA expression.Clinical and translational medicine · 2022
    Article
  13. Article
  14. Review
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

9 authors at 4 institutions in 2 countries.

Amy E LoatsSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.ORCID 0000-0002-2110-6707
Samantha CarreraSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.
Anna F FlemingSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.ORCID 0000-0002-2813-5690
Abigail R E RobertsSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.
Alice SherrardSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.
Eneda ToskaDepartment of Biological Sciences, University at Buffalo, Buffalo, NY 14260.
Alexander J MoorhouseSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom.ORCID 0000-0002-1626-6087
Kathryn F MedlerDepartment of Biological Sciences, University at Buffalo, Buffalo, NY 14260.ORCID 0000-0001-9664-3606
Stefan G E RobertsSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, BS8 1TD, United Kingdom Stefan.Roberts@bristol.ac.uk.ORCID 0000-0002-7535-6365
University of Bristol · GBJohns Hopkins University · USUniversity at Buffalo, State University of New York · USYale University · US

Funding

Functional analysis of the WT1-BASP1 transcriptional repressor complexR01GM098609 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MEDLER, KATHRYN, ROBERTS, STEFAN · 2012 to 2015
$1.2M
Biotechnology and Biological Sciences Research Council BB/T001925/1Medical Research Council MR/K001027/1NIGMS NIH HHS R01 GM098609Wellcome TrustWellcome Trust 083474
6 · The paper itself

Abstract

Lipids are present within the cell nucleus, where they engage with factors involved in gene regulation. Cholesterol associates with chromatin in vivo and stimulates nucleosome packing in vitro, but its effects on specific transcriptional responses are not clear. Here, we show that the lipidated Wilms tumor 1 (WT1) transcriptional corepressor, brain acid soluble protein 1 (BASP1), interacts with cholesterol in the cell nucleus through a conserved cholesterol interaction motif. We demonstrate that BASP1 directly recruits cholesterol to the promoter region of WT1 target genes. Mutation of BASP1 to ablate its interaction with cholesterol or the treatment of cells with drugs that block cholesterol biosynthesis inhibits the transcriptional repressor function of BASP1. We find that the BASP1-cholesterol interaction is required for BASP1-dependent chromatin remodeling and the direction of transcription programs that control cell differentiation. Our study uncovers a mechanism for gene-specific targeting of cholesterol where it is required to mediate transcriptional repression.

Indexed as

Transcription, GeneticCell NucleusCholesterolDown-RegulationHumansK562 CellsMembrane ProteinsNerve Tissue ProteinsPromoter Regions, GeneticProtein BindingRepressor ProteinsBASP1 protein, humanCholesterolMembrane ProteinsNerve Tissue ProteinsRepressor ProteinsBASP1cholesterolchromatintranscriptionWT1

Identifiers

PMID34266955
PMCPMC8307447
OpenAlexW3182957529

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.