Language

English

Publication Date

4-4-2025

Journal

Journal of Proteome Research

DOI

10.1021/acs.jproteome.4c00877

PMID

40020221

PMCID

PMC12903780

PubMedCentral® Posted Date

2-28-2026

PubMedCentral® Full Text Version

Author MSS

Abstract

Histone proteoforms, often presenting multiple co-occurring post-translational modifications (PTMs), are central to chromatin regulation and gene expression. A proteoform is a specific form of a protein that includes variations arising from genetic changes, alternative RNA splicing, proteolytic processing, and PTMs. Genome-indexed histone proteoforms define the histone code, influencing cellular phenotype by dictating DNA interacting partners. Understanding the dynamics of histone proteoforms is essential for elucidating chromatin-based regulatory mechanisms. Advances in middle-down and top-down proteomics enable accurate identification and quantitation of thousands of proteoforms in a single run. However, the resulting data complexity presents significant challenges for analysis and visualization. Here, we introduce two new computational methods to analyze the dynamics of histone PTMs and demonstrate their use in mouse organs during aging. The score that we term ‘Normalized Interplay’ addresses limitations of the original crosstalk score ‘Interplay’ providing a more complete and accurate measure of PTM crosstalk. The second score, Δ⁢𝐼 or ‘Directional Interplay’ is an asymmetric measure quantifying the magnitude and directionality of crosstalk between PTMs. Applying our two-stage scoring approach to data from CrosstalkDB reveals the dynamics of histone H3 modifications during aging. The source code is available at https://github.com/k-p4/ptm_interplay_scoring.

Keywords

Animals, Histones, Protein Processing, Post-Translational, Mice, Proteomics, Aging, Histone Code, Chromatin, Proteoforms, Post-translational Modifications, Interplay, Crosstalk, Top-down Proteomics, Epigenetics, Chromatin, Aging

Published Open-Access

yes

nihms-2137014-f0001.jpg (192 kB)
Graphical Abstract

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.