Evidence map›Paper›PMID 30150385›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks.

James J Galligan, James A Wepy, Matthew D Streeter, Philip J Kingsley, Michelle M Mitchener, Orrette R Wauchope, William N Beavers, Kristie L Rose, Tina Wang, David A Spiegel and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

126 citing papers in PubMed, 185 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Linking cellular metabolism to chromatin modifications in plants.Journal of integrative plant biology · 2026
    Review
  5. Article
  6. Non-Enzymatic MGO-Glycation of SRSF2 Drives RNA Mis-Splicing.Journal of the American Chemical Society · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Discovery of Glycation-Derived Cross-links at Arginine.Journal of the American Chemical Society · 2026
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Glyoxalase 1 is a proadipogenic gene.The Journal of biological chemistry · 2025
    Article
  18. Article
  19. A Chemical Mechanistic Path Leads the Way to Cellular Argpyrimidine.Journal of the American Chemical Society · 2025
    Article
  20. Article

66 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

11 authors at 2 institutions in 1 country.

James J GalliganA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.ORCID 0000-0002-5612-0680
James A WepyA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.
Matthew D StreeterDepartment of Chemistry, Yale University, New Haven, CT 06520.
Philip J KingsleyA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.
Michelle M MitchenerA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.
Orrette R WauchopeA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.
William N BeaversA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232.
Kristie L RoseMass Spectrometry Resource Center, Vanderbilt University, Nashville, TN 37232.
Tina WangDepartment of Chemistry, Yale University, New Haven, CT 06520.
David A SpiegelDepartment of Chemistry, Yale University, New Haven, CT 06520.
Lawrence J MarnettA.B. Hancock Memorial Laboratory for Cancer Research, Vanderbilt University, Nashville, TN 37232; larry.marnett@vanderbilt.edu.
Vanderbilt University · USYale University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
THE ROLE OF ENDOCANNABINOIDS AND THEIR RECEPTORS IN COLORECTAL CANCERP01CA077839 · NCI · VANDERBILT UNIVERSITY · PI HLA, TIMOTHY TUN · 1999 to 2016
$17.8M
Pharmacogenomics of Arrhythmia TherapyU19HL065962 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RODEN, DAN M · 2010 to 2014
$17.4M
Understanding and preventing HLA-associated drug reactionsP50GM115305 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2015 to 2019
$13.0M
VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced GenomicsG20RR030956 · NCRR · VANDERBILT UNIVERSITY · PI PIETENPOL, JENNIFER A · 2010 to 2010
$8.7M
Chemistry-Biology Interface Training GrantT32GM065086 · NIGMS · VANDERBILT UNIVERSITY · PI BACHMANN, BRIAN O, SULIKOWSKI, GARY ALLEN · 2002 to 2022
$7.0M
Chemistry and Biology of Malondialdehyde DNA AdductsR37CA087819 · NCI · VANDERBILT UNIVERSITY · PI MARNETT, LAWRENCE J. · 2005 to 2014
$4.2M
CHEMISTRY AND BIOLOGY OF MALONDIALDEHYDE DNA ADDUCTSR01CA087819 · NCI · VANDERBILT UNIVERSITY · PI MARNETT, LAWRENCE J. · 2000 to 2020
$4.0M
Acquisition of an AB Sciex Qtrap 6500 LC/MS/MS SystemS10OD017997 · OD · VANDERBILT UNIVERSITY · PI MARNETT, LAWRENCE J. · 2015 to 2015
$450k
NCI NIH HHS P01 CA077839NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA087819NCI NIH HHS R37 CA087819NCRR NIH HHS G20 RR030956NCRR NIH HHS UL1 RR024975NEI NIH HHS P30 EY008126NHLBI NIH HHS U19 HL065962NIDDK NIH HHS P30 DK058404NIGMS NIH HHS P50 GM115305NIGMS NIH HHS T32 GM065086NIH HHS S10 OD017997
6 · The paper itself

Abstract

Histone posttranslational modifications (PTMs) regulate chromatin dynamics, DNA accessibility, and transcription to expand the genetic code. Many of these PTMs are produced through cellular metabolism to offer both feedback and feedforward regulation. Herein we describe the existence of Lys and Arg modifications on histones by a glycolytic by-product, methylglyoxal (MGO). Our data demonstrate that adduction of histones by MGO is an abundant modification, present at the same order of magnitude as Arg methylation. These modifications were detected on all four core histones at critical residues involved in both nucleosome stability and reader domain binding. In addition, MGO treatment of cells lacking the major detoxifying enzyme, glyoxalase 1, results in marked disruption of H2B acetylation and ubiquitylation without affecting H2A, H3, and H4 modifications. Using RNA sequencing, we show that MGO is capable of altering gene transcription, most notably in cells lacking GLO1. Finally, we show that the deglycase DJ-1 protects histones from adduction by MGO. Collectively, our findings demonstrate the existence of a previously undetected histone modification derived from glycolysis, which may have far-reaching implications for the control of gene expression and protein transcription linked to metabolism.

Indexed as

PyruvaldehydeArginineHEK293 CellsHistonesHumansLactoylglutathione LyaseProtein Processing, Post-TranslationalTranscription, GeneticArginineGLO1 protein, humanHistonesLactoylglutathione LyasePyruvaldehydeDJ-1glyoxalase 1histonemethylglyoxalQuARKMod

Identifiers

PMID30150385
PMCPMC6140490
OpenAlexW2889368382

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.