Evidence map›Paper›PMID 17967868›Full record

ArticleMolecular and cellular biology2008

The mammalian ortholog of Drosophila MOF that acetylates histone H4 lysine 16 is essential for embryogenesis and oncogenesis.

Arun Gupta, T Geraldine Guerin-Peyrou, Girdhar G Sharma, Changwon Park, Manjula Agarwal, Ramesh K Ganju, Shruti Pandita, Kyunghee Choi, Saraswati Sukumar, Raj K Pandita and 2 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

140 citing papers in PubMed, 220 citations in OpenAlex.

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  17. Acetyltransferase in cardiovascular disease and aging.The journal of cardiovascular aging · 2024
    Article
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  20. Article

80 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 3 institutions in 1 country.

Arun GuptaDepartment of Radiation Oncology, Washington University School of Medicine, 4511 Forest Park, St. Louis, MO 63108, USA.
T Geraldine Guerin-Peyrou
Girdhar G Sharma
Changwon Park
Manjula Agarwal
Ramesh K Ganju
Shruti Pandita
Kyunghee Choi
Saraswati Sukumar
Raj K Pandita
Thomas Ludwig
Tej K Pandita
Washington University in St. Louis · USCancer Genetics (United States) · USHarvard University · US

Funding

The role of PTEN in basal-like breast cancerP01CA097403 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BAER, RICHARD J · 2003 to 2013
$18.2M
Functional Characterization of the Mammalian MOF Gene ProductR01CA123232 · NCI · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 2007 to 2011
$1.5M
NCI NIH HHS CA10445NCI NIH HHS CA123232NCI NIH HHS P01 CA097403NCI NIH HHS P01 CA97403NCI NIH HHS R01 CA123232
6 · The paper itself

Abstract

The mammalian ortholog of the Drosophila MOF (males absent on the first) gene product is a histone H4 lysine 16-specific acetyltransferase. Recent studies have shown that depletion of human MOF (hMOF) in human cell lines leads to genomic instability, spontaneous chromosomal aberrations, cell cycle defects, altered nuclear morphology, reduced transcription of certain genes, and defective DNA damage response to ionizing radiation (IR). Here we show that MOF plays an essential role in mammals during embryogenesis and oncogenesis. Ablation of the mouse Mof gene (mMof) by gene targeting resulted in early embryonic lethality and cell death. Lethality correlated with the loss of H4 lysine 16 acetylation (H4K16ac) and could not be rescued by concomitant inactivation of ATM or p53. In comparison to primary cells or normal tissue, all immortalized human normal and tumor cell lines and primary tumors demonstrated similar or elevated hMOF and H4K16ac levels. Accordingly, MOF overexpression correlated with increased cellular proliferation, oncogenic transformation, and tumor growth. Thus, these data reveal that the acetylation of histone H4 at K16 by MOF is an epigenetic signature of cellular proliferation common to both embryogenesis and oncogenesis and that MOF is an essential factor for embryogenesis and oncogenesis.

Indexed as

AcetylationAnimalsCell ProliferationCells, CulturedCell Transformation, NeoplasticDrosophila melanogasterDrosophila ProteinsEmbryo LossEmbryo, MammalianGene DeletionGene Expression RegulationHistone AcetyltransferasesHistonesMaleMiceNuclear ProteinsDrosophila ProteinsHistone AcetyltransferasesHistonesKAT8 protein, humanKat8 protein, mousemof protein, DrosophilaNuclear ProteinsRNA, MessengerTumor Suppressor Protein p53

Identifiers

PMID17967868
PMCPMC2223300
OpenAlexW2130304567

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.