Evidence map›Paper›PMID 16481466›Full record

ArticleGenes & development2006

Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors.

Lei Wang, Harini Rajan, Jeffrey L Pitman, Michael McKeown, Chih-Cheng Tsai

Abstract read
In one paragraph

Article in Genes & development, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–field-weighted citation impact
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

53 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. High-Content Drug Discovery Targeting Molecular Bladder Cancer Subtypes.International journal of molecular sciences · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Machine Learning Analysis IdentifiesG3 (Bethesda, Md.) · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Novel genetic causes for cerebral visual impairment.European journal of human genetics : EJHG · 2016
    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

5 authors.

Lei WangDepartment of Physiology and Biophysics, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Harini Rajan
Jeffrey L Pitman
Michael McKeown
Chih-Cheng Tsai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drosophila Tailless (Tll) is an orphan nuclear receptor involved in embryonic segmentation and neurogenesis. Although Tll exerts potent transcriptional repressive effects, the underlying molecular mechanisms have not been determined. Using the established regulation of knirps by tll as a paradigm, we report that repression of knirps by Tll involves Atrophin, which is related to vertebrate Atrophin-1 and Atrophin-2. Atrophin interacts with Tll physically and genetically, and both proteins localize to the same knirps promoter region. Because Atrophin proteins interact with additional nuclear receptors and Atrophin-2 selectively binds histone deacetylase 1/2 (HDAC1/2) through its ELM2 (EGL-27 and MTA1 homology 2)/SANT (SWI3/ADA2/N-CoR/TFIII-B) domains, our study establishes that Atrophin proteins represent a novel class of nuclear receptor corepressors.

Indexed as

AlanineAmino Acid MotifsAmino Acid SequenceAmino Acid SubstitutionAnimalsbeta-GalactosidaseCell LineConserved SequenceDNA-Binding ProteinsDrosophilaDrosophila ProteinsEmbryo, NonmammalianGlutathione TransferaseHistone DeacetylasesHumansModels, BiologicalAlaninebeta-GalactosidaseDNA-Binding ProteinsDrosophila ProteinsGlutathione Transferasegug protein, DrosophilaHistone Deacetylaseskni protein, DrosophilaNCOR1 protein, humanNuclear ProteinsNuclear Receptor Co-Repressor 1Recombinant Fusion ProteinsRepressor ProteinsTLL protein, DrosophilaTranscription Factors

Identifiers

PMID16481466
PMCPMC1410805

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.