Evidence map›Paper›PMID 25569455›Full record

ArticleVirology2015

Acetylation of the c-MYC oncoprotein is required for cooperation with the HTLV-1 p30(II) accessory protein and the induction of oncogenic cellular transformation by p30(II)/c-MYC.

Megan M Romeo, Bookyung Ko, Janice Kim, Rebecca Brady, Hayley C Heatley, Jeffrey He, Carolyn K Harrod, Braden Barnett, Lee Ratner, Michael D Lairmore and 5 more

Open access · greenAbstract read
In one paragraph

Article in Virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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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

15 authors at 7 institutions in 4 countries.

Megan M RomeoLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Bookyung KoLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Janice KimLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Rebecca BradyLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Hayley C HeatleyLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Jeffrey HeLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Carolyn K HarrodLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Braden BarnettLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA.
Lee RatnerDepartments of Medicine and Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michael D LairmoreUniversity of California-Davis, School of Veterinary Medicine, One Shields Avenue, Davis, CA 95618, USA.
Ernest MartinezDepartment of Biochemistry, University of California, Riverside, CA 92521, USA.
Bernhard LüscherInstitute of Biochemistry, Klinikum, RWTH Aachen University, Pauwelsstrasse 30, 52057 Aachen, Germany.
Craig N RobsonNorthern Institute for Cancer Research, Newcastle University, The Medical School, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Marie HenrikssonDepartment of Microbiology, Cell and Tumor Biology, Karolinska Institutet, Stockholm, Sweden.
Robert HarrodLaboratory of Molecular Virology, Department of Biological Sciences, and The Dedman College Center for Drug Discovery, Design, and Delivery, Southern Methodist University, Dallas, TX 75275-0376, USA. Electronic address: rharrod@smu.edu.
Southern Methodist University · USKarolinska Institutet · SENewcastle University · GBRWTH Aachen University · DEUniversity of California, Davis · USUniversity of California, Riverside · USWashington University in St. Louis · US

Funding

Role of Inflammation in Tax-mediated TumorigenesisP01CA100730 · NCI · WASHINGTON UNIVERSITY · PI Malachi Griffith · 2003 to 2026
$44.8M
PROLIFERATIVE EFFECTS OF HTLV1R01CA063417 · NCI · WASHINGTON UNIVERSITY · PI RATNER, LEE · 1995 to 2017
$3.7M
Coordinate Regulation of p53 and c-MYC in an HTLV-1 Model of CarcinogenesisR15CA158945 · NCI · SOUTHERN METHODIST UNIVERSITY · PI HARROD, ROBERT L. · 2012 to 2012
$436k
Modulation of c-MYC Functions in an HTLV-1 Model for CarcinogenesisR15CA139425 · NCI · SOUTHERN METHODIST UNIVERSITY · PI HARROD, ROBERT L. · 2009 to 2009
$218k
NCI NIH HHS 1R15CA139425-01NCI NIH HHS 1R15CA158945-01A1NCI NIH HHS P01 CA100730NCI NIH HHS R01 CA063417NCI NIH HHS R15 CA139425NCI NIH HHS R15 CA158945
6 · The paper itself

Abstract

The human T-cell leukemia retrovirus type-1 (HTLV-1) p30(II) protein is a multifunctional latency-maintenance factor that negatively regulates viral gene expression and deregulates host signaling pathways involved in aberrant T-cell growth and proliferation. We have previously demonstrated that p30(II) interacts with the c-MYC oncoprotein and enhances c-MYC-dependent transcriptional and oncogenic functions. However, the molecular and biochemical events that mediate the cooperation between p30(II) and c-MYC remain to be completely understood. Herein we demonstrate that p30(II) induces lysine-acetylation of the c-MYC oncoprotein. Acetylation-defective c-MYC Lys→Arg substitution mutants are impaired for oncogenic transformation with p30(II) in c-myc(-/-) HO15.19 fibroblasts. Using dual-chromatin-immunoprecipitations (dual-ChIPs), we further demonstrate that p30(II) is present in c-MYC-containing nucleoprotein complexes in HTLV-1-transformed HuT-102 T-lymphocytes. Moreover, p30(II) inhibits apoptosis in proliferating cells expressing c-MYC under conditions of genotoxic stress. These findings suggest that c-MYC-acetylation is required for the cooperation between p30(II)/c-MYC which could promote proviral replication and contribute to HTLV-1-induced carcinogenesis.

Indexed as

Cell Transformation, NeoplasticAcetylationAmino Acid MotifsCell ProliferationCell Transformation, ViralHTLV-I InfectionsHumansHuman T-lymphotropic virus 1Proto-Oncogene Proteins c-mycRetroviridae ProteinsProto-Oncogene Proteins c-mycRetroviridae Proteinstof protein, Human T-lymphotropic virus 1AcetylationApoptosisc-MYCHTLV-1p30Transformation

Identifiers

PMID25569455
PMCPMC4323988
OpenAlexW2000539064

What OpenQuestion holds

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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.