Evidence map›Paper›PMID 19350571›Full record

ArticleJournal of cellular biochemistry2009

HACE1: A novel repressor of RAR transcriptional activity.

Jianhua Zhao, Zhenping Zhang, Zivjena Vucetic, Kenneth J Soprano, Dianne Robert Soprano

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Common variations withinOncoTargets and therapy · 2017
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. HACE1 (HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1).Atlas of genetics and cytogenetics in oncology and haematology · 2012
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. The Ski protein negatively regulates Siah2-mediated HDAC3 degradation.Biochemical and biophysical research communications · 2010
    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 at 1 institution in 1 country.

Jianhua ZhaoDepartment of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Zhenping Zhang
Zivjena Vucetic
Kenneth J Soprano
Dianne Robert Soprano
Temple University · US

Funding

RETINOIDS FOR TREATMENT OF OVARIAN CARCINOMAR01CA064945 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI SOPRANO, KENNETH J · 1994 to 2007
$1.9M
Acinus: A Novel Corepressor of RAR-Regulated Gene ExpressionR01DK067558 · NIDDK · TEMPLE UNIV OF THE COMMONWEALTH · PI SOPRANO, DIANNE R · 2007 to 2011
$1.6M
STRUCTURE AND FUNCTION OF RETINOIC ACID RECEPTORSR01DK044517 · NIDDK · TEMPLE UNIVERSITY · PI SOPRANO, DIANNE R · 1992 to 2005
$1.4M
NCI NIH HHS CA64945NCI NIH HHS R01 CA064945NIDDK NIH HHS DK44517NIDDK NIH HHS DK67558NIDDK NIH HHS R01 DK044517NIDDK NIH HHS R01 DK067558
6 · The paper itself

Abstract

The diverse biological actions of retinoic acid (RA) are mediated by RA receptors (RARs) and retinoid X receptors (RXRs). While the coregulatory proteins that interact with the ligand-dependent AF-2 in the E region are well studied, the ligand-independent N-terminal AF-1 domain-interacting partners and their influence(s) on the function of RARs are poorly understood. HECT domain and Ankyrin repeat containing E3 ubiquitin-protein ligase (HACE1) was isolated as a RARbeta(3) AB region interacting protein. HACE1 interacts with RARbeta(3) both in in vitro GST pull-down and in cell-based coprecipitation assays. The interaction sites map to the N terminus of RARbeta(3) and the C terminus of HACE1. HACE1 functionally represses the transcriptional activity of RARalpha(1), RARbeta isoforms 1, 2, and 3, but not RARgamma(1) in luciferase reporter assays. In addition, HACE1 represses the endogenous RAR-regulated genes CRABP II, RIG1 and RARbeta(2), but not RAI3 in CAOV3 cells. Mutation of the putative catalytic cysteine (C876 of LF HACE1), which is indispensable for its E3 ubiquitin ligase activity, does not alter the repressive effect of HACE1 on the transcriptional activity of RARbeta(3). On the other hand, HACE1 inhibits the RA dependent degradation of RARbeta(3). It is possible that the repression of RAR-regulated transcription by HACE1 is due to its ability to inhibit the RA-dependent degradation of RARs.

Indexed as

Transcription, GeneticAnimalsChlorocebus aethiopsCOS CellsHumansMiceNIH 3T3 CellsReceptors, Retinoic AcidRepressor ProteinsUbiquitin-Protein LigasesHACE1 protein, humanReceptors, Retinoic AcidRepressor ProteinsUbiquitin-Protein Ligases

Identifiers

PMID19350571
PMCPMC2736627
OpenAlexW2068004351

What OpenQuestion holds

Textmetadata
LicenceTDM
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.