Evidence map›Paper›PMID 26296975›Full record

ArticleOncotarget2015

Zinc finger transcription factor CASZ1 interacts with histones, DNA repair proteins and recruits NuRD complex to regulate gene transcription.

Zhihui Liu, Norris Lam, Carol J Thiele

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. 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
1.5field-weighted citation impact, top 18% 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, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Biomedicines · 2023
    Review
  7. Article
  8. Article
  9. Chromatin Remodeling in the Brain-aInternational journal of molecular sciences · 2021
    Review
  10. CASZ1b is a novel transcriptional corepressor of mineralocorticoid receptor.Hypertension research : official journal of the Japanese Society of Hypertension · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Casz1 controls higher-order nuclear organization in rod photoreceptors.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Article
  16. Effects of CASZI on bronchopulmonary development of neonatal rats.Experimental and therapeutic medicine · 2017
    Article
  17. Article
  18. Article
  19. 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.

Zhihui LiuPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Norris LamPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Carol J ThielePediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
National Cancer Institute · US

Funding

Intramural NIH HHS
6 · The paper itself

Abstract

The zinc finger transcription factor CASZ1 has been found to control neural fate-determination in flies, regulate murine and frog cardiac development, control murine retinal cell progenitor expansion and function as a tumor suppressor gene in humans. However, the molecular mechanism by which CASZ1 regulates gene transcription to exert these diverse biological functions has not been described. Here we identify co-factors that are recruited by CASZ1b to regulate gene transcription using co-immunoprecipitation (co-IP) and mass spectrometry assays. We find that CASZ1b binds to the nucleosome remodeling and histone deacetylase (NuRD) complex, histones and DNA repair proteins. Mutagenesis of the CASZ1b protein assay demonstrates that the N-terminus of CASZ1b is required for NuRD binding, and a poly(ADP-ribose) binding motif in the CASZ1b protein is required for histone H3 and DNA repair proteins binding. The N-terminus of CASZ1b fused to an artificial DNA-binding domain (GAL4DBD) causes a significant repression of transcription (5xUAS-luciferase assay), which could be blocked by treatment with an HDAC inhibitor. Realtime PCR results show that the transcriptional activity of CASZ1b mutants that abrogate NuRD or histone H3/DNA binding is significantly decreased. This indicates a model in which CASZ1b binds to chromatin and recruits NuRD complexes to orchestrate epigenetic-mediated transcriptional programs.

Indexed as

DNA RepairGene Expression Regulation, NeoplasticAmino Acid MotifsAnimalsCell LineDNA-Binding ProteinsEpigenesis, GeneticHEK293 CellsHistonesHumansImmunoprecipitationMass SpectrometryMi-2 Nucleosome Remodeling and Deacetylase ComplexMiceMutagenesisMutationCASZ1 protein, humanCASZ1 protein, mouseDNA-Binding ProteinsHistonesMi-2 Nucleosome Remodeling and Deacetylase ComplexNucleosomesRecombinant Fusion ProteinsTranscription FactorsCASZ1cofactorsDNA repair proteinNuRD complextumor suppressor

Identifiers

PMID26296975
PMCPMC4695013
OpenAlexW1128957151

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.