Evidence map›Paper›PMID 20479123›Full record

ArticleMolecular and cellular biology2010

MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair.

Girdhar G Sharma, Sairei So, Arun Gupta, Rakesh Kumar, Christelle Cayrou, Nikita Avvakumov, Utpal Bhadra, Raj K Pandita, Matthew H Porteus, David J Chen and 2 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 194 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
194citing papers in PubMed, 1 pooled it
10.3field-weighted citation impact, top 1% 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

194 citing papers in PubMed, 1 synthesis or guideline pooled it, 306 citations in OpenAlex.

  1. Pooled it
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  16. Mechanism of Histone Arginine Methylation Dynamic Change in Cellular Stress.International journal of molecular sciences · 2024
    Article
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134 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 3 countries.

Girdhar G SharmaWashington University School of Medicine, St. Louis, Missouri 63108, USA.
Sairei So
Arun Gupta
Rakesh Kumar
Christelle Cayrou
Nikita Avvakumov
Utpal Bhadra
Raj K Pandita
Matthew H Porteus
David J Chen
Jacques Cote
Tej K Pandita
The University of Texas Southwestern Medical Center · USWashington University in St. Louis · USUniversité Laval · CACentre for Cellular and Molecular Biology · IN

Funding

Roles of DNA PK in DNA Double Strand Break RepairR37CA050519 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHEN, DAVID J · 2003 to 2011
$3.5M
CHROMATIN MODIFYING FACTORS CONTROL RADIATION RESPONSE AND GENOMIC STABILITYR01CA129537 · NCI · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 2008 to 2018
$3.3M
Functional Characterization of the Mammalian MOF Gene ProductR01CA123232 · NCI · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 2007 to 2011
$1.5M
CHROMATIN-TELOMERE STRUCTURE AND AT GENOMIC SENSITIVITYR01NS034746 · NINDS · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 1996 to 2005
$1.2M
ROLES OF DNA PK IN DNA DOUBLE STRAND BREAK REPAIRR01CA050519 · NCI · UNIVERSITY OF CALIF-LOS ALAMOS NAT LAB · PI CHEN, DAVID J · 1989 to 2001
$946k
CHROMATIN STRUCTURE AND DNA REPAIRR13CA130756 · NCI · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 2007 to 2011
$14k
CIHR 64289-2CIHR 87253-1CIHR MOP-64289NCI NIH HHS CA10445NCI NIH HHS CA123232NCI NIH HHS CA 50519NCI NIH HHS R01 CA050519NCI NIH HHS R01 CA123232NCI NIH HHS R01 CA129537NCI NIH HHS R13 CA130756NCI NIH HHS R37 CA050519NINDS NIH HHS R01 NS034746
6 · The paper itself

Abstract

The human MOF gene encodes a protein that specifically acetylates histone H4 at lysine 16 (H4K16ac). Here we show that reduced levels of H4K16ac correlate with a defective DNA damage response (DDR) and double-strand break (DSB) repair to ionizing radiation (IR). The defect, however, is not due to altered expression of proteins involved in DDR. Abrogation of IR-induced DDR by MOF depletion is inhibited by blocking H4K16ac deacetylation. MOF was found to be associated with the DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a protein involved in nonhomologous end-joining (NHEJ) repair. ATM-dependent IR-induced phosphorylation of DNA-PKcs was also abrogated in MOF-depleted cells. Our data indicate that MOF depletion greatly decreased DNA double-strand break repair by both NHEJ and homologous recombination (HR). In addition, MOF activity was associated with general chromatin upon DNA damage and colocalized with the synaptonemal complex in male meiocytes. We propose that MOF, through H4K16ac (histone code), has a critical role at multiple stages in the cellular DNA damage response and DSB repair.

Indexed as

DNA Breaks, Double-StrandedDNA DamageAcetylationAtaxia Telangiectasia Mutated ProteinsBase SequenceCell Cycle ProteinsCell LineChromatinDNA-Activated Protein KinaseDNA-Binding ProteinsDNA RepairFemaleHistone AcetyltransferasesHistone Deacetylase InhibitorsHistonesHL-60 CellsAtaxia Telangiectasia Mutated ProteinsATM protein, humanCell Cycle ProteinsChromatinDNA-Activated Protein KinaseDNA-Binding ProteinsH2AX protein, humanHistone AcetyltransferasesHistone Deacetylase InhibitorsHistonesKAT8 protein, humanLysineNuclear ProteinsPRKDC protein, humanProtein Serine-Threonine KinasesRNA, Small InterferingTumor Suppressor Proteins

Identifiers

PMID20479123
PMCPMC2897562
OpenAlexW2157172346

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.