Evidence map›Paper›PMID 15639232›Full record

ArticleArchives of biochemistry and biophysics2005

BCL11A-dependent recruitment of SIRT1 to a promoter template in mammalian cells results in histone deacetylation and transcriptional repression.

Thanaset Senawong, Valerie J Peterson, Mark Leid

Open access · greenAbstract read
In one paragraph

Article in Archives of biochemistry and biophysics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. BCL11A Expression in Non-Small Cell Lung Cancers.International journal of molecular sciences · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. SIRT1 activates the expression of fetal hemoglobin genes.American journal of hematology · 2017
    Article
  13. The Specification of Cortical Subcerebral Projection Neurons Depends on the Direct Repression of TBR1 by CTIP1/BCL11a.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  14. Sirtuins in epigenetic regulation.Chemical reviews · 2015
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Role of the transcription factor Bcl11b in development and lymphomagenesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2012
    Review
  20. Mammalian Sirt1: insights on its biological functions.Cell communication and signaling : CCS · 2011
    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

3 authors at 1 institution in 1 country.

Thanaset SenawongProgram in Molecular and Cellular Biology, Oregon State University, Corvallis, OR 97331, USA.
Valerie J Peterson
Mark Leid
Oregon State University · US

Funding

Reducing Susceptibility to Environmental Stress Throughout the Life SpanP30ES000210 · NIEHS · OREGON STATE UNIVERSITY · PI BECKMAN, JOSEPH S · 1985 to 2015
$21.4M
Transcriptional Repression Mechanisms of COUP ProteinsR01GM060852 · NIGMS · OREGON STATE UNIVERSITY · PI LEID, MARK E · 2001 to 2004
$1.1M
NIEHS NIH HHS ES00210NIEHS NIH HHS P30 ES000210NIGMS NIH HHS GM60852NIGMS NIH HHS R01 GM060852
6 · The paper itself

Abstract

The B cell leukemia 11A protein (BCL11A/Evi9/CTIP1) has been implicated in hematopoietic cell development and malignancies. BCL11A is a transcriptional repressor that binds directly to a GC-rich motif and is also recruited to a promoter template via interaction with the orphan nuclear receptor, chicken ovalbumin upstream promoter transcription factor II. In both cases, BCL11A-mediated transcriptional repression is only minimally reversed by trichostatin A, suggesting the possible lack of involvement of class I or II histone deacetylases. Nonetheless, chromatin immunoprecipitation assays revealed that expression of BCL11A in mammalian cells resulted in deacetylation of histones H3 and/or H4 that were associated with the promoter region of a reporter gene. BCL11A-mediated transcriptional repression, as well as deacetylation of histone H3/H4 in BCL11A-transfected cells, was partially reversed by nicotinamide, an inhibitor of class III histone deacetylases such as SIRT1. SIRT1 was found to interact directly with BCL11A and was recruited to the promoter template in a BCL11A-dependent manner leading to transcriptional repression. These findings define a role for SIRT1 in transcriptional repression mediated by BCL11A in mammalian cells.

Indexed as

Promoter Regions, GeneticTranscription, GeneticAmino Acid MotifsAnimalsCarrier ProteinsCell LineChromatin ImmunoprecipitationGene DeletionGenes, ReporterGlutathione TransferaseHistone DeacetylasesHistonesHumansHydroxamic AcidsImmunoprecipitationModels, GeneticBCL11A protein, humanCarrier ProteinsGlutathione TransferaseHistone DeacetylasesHistonesHydroxamic AcidsNiacinamideNuclear ProteinsRepressor ProteinsSIRT1 protein, humanSirtuin 1Sirtuinstrichostatin A

Identifiers

PMID15639232
PMCPMC2819353
OpenAlexW2012994927

What OpenQuestion holds

Textmetadata
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.