Evidence map›Paper›PMID 27555324›Full record

ArticleThe Journal of biological chemistry2016

A Novel Role of Chromodomain Protein CBX8 in DNA Damage Response.

Jay Oza, Bratati Ganguly, Atul Kulkarni, Vasudeva Ginjala, Ming Yao, Shridar Ganesan

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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  7. Article
  8. Review
  9. International journal of biological sciences · 2018
    Article
  10. Review
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jay OzaFrom the MD-PhD Program, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey 08903.
Bratati Gangulythe Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, and.
Atul Kulkarnithe Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, and.
Vasudeva Ginjalathe Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, and.
Ming Yaothe Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, and.
Shridar Ganesanthe Department of Cellular and Molecular Pharmacology, Rutgers-Graduate School of Biomedical Sciences, Piscataway, New Jersey 08854, ganesash@cinj.rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
53BP1-Mediated Regulation of DNA Repair and ChemoresistanceR01CA169182 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GANESAN, SHRIDAR · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA169182
6 · The paper itself

Abstract

Induction of DNA damage induces a dynamic repair process involving DNA repair factors and epigenetic regulators. Chromatin alterations must occur for DNA repair factors to gain access to DNA lesions and restore original chromatin configuration to preserve the gene expression profile. We characterize the novel role of CBX8, a chromodomain-containing protein with established roles in epigenetic regulation in DNA damage response. CBX8 protein rapidly accumulates at the sites of DNA damage within 30 s and progresses to accumulate until 4 min before gradually dispersing back to its predamage distribution by 15 min. CBX8 recruitment to the sites of DNA damage is dependent upon PARP1 activation and not dependent on ATM activation. CBX8 biochemically interacts with TRIM33, and its recruitment to DNA damage is also dependent on the presence of TRIM33. Knockdown of CBX8 using siRNA significantly reduces the efficiency of both homologous and the other non-homologous recombination, as well as increases sensitivity of cells to ionizing radiation. These findings demonstrate that CBX8 functions in the PARP-dependent DNA damage response partly through interaction with TRIM33 and is required for efficient DNA repair.

Indexed as

DNA DamageAnimalsAtaxia Telangiectasia Mutated ProteinsDNA RepairEpigenesis, GeneticHumansMiceMice, KnockoutMitochondrial Membrane Transport ProteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Protein BindingTranscription FactorsAtaxia Telangiectasia Mutated ProteinsCBX8 protein, humanCbx8 protein, mouseMitochondrial Membrane Transport ProteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Transcription FactorsTRIM33 protein, humanTrim33 protein, mousecancer biologyCBX8chromatinChromodomain proteinDNA damageDNA damage responseDNA repairPARP1polycombTRIM33

Identifiers

PMID27555324
PMCPMC5087711
OpenAlexW2508697143

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.