Systematic quantitative analysis of H2A and H2B variants by targeted proteomics

BACKGROUNDHistones organize DNA into chromatin through a variety of processes. Among them, a vast diversity of histone variants can be incorporated into chromatin and finely modulate its organization and functionality. Classically, the study of histone variants has largely relied on antibody-based a...

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Bibliographic Details
Published in:Epigenetics & chromatin 2018-01, Vol.11 (1), p.2-2, Article 2
Main Authors: El Kennani, Sara, Adrait, Annie, Permiakova, Olga, Hesse, Anne-Marie, Ialy-Radio, Come, Ferro, Myriam, Brun, Virginie, Cocquet, Julie, Govin, Jnrome, Pflieger, Delphine
Format: Article
Language:English
Subjects:
Analysis
Antibodies
Biochemistry, Molecular Biology
Chromatin
DNA binding proteins
Genomics
Health aspects
Histone variants
Histones
Life Sciences
Peptides
PRM
Proteomics
SRM
Targeted proteomics
Viral antibodies
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Summary:BACKGROUNDHistones organize DNA into chromatin through a variety of processes. Among them, a vast diversity of histone variants can be incorporated into chromatin and finely modulate its organization and functionality. Classically, the study of histone variants has largely relied on antibody-based assays. However, antibodies have a limited efficiency to discriminate between highly similar histone variants. RESULTSIn this study, we established a mass spectrometry-based analysis to address this challenge. We developed a targeted proteomics method, using selected reaction monitoring or parallel reaction monitoring, to quantify a maximum number of histone variants in a single multiplexed assay, even when histones are present in a crude extract. This strategy was developed on H2A and H2B variants, using 55 peptides corresponding to 25 different histone sequences, among which a few differ by a single amino acid. The methodology was then applied to mouse testis extracts in which almost all histone variants are expressed. It confirmed the abundance profiles of several testis-specific histones during successive stages of spermatogenesis and the existence of predicted H2A.L.1 isoforms. This methodology was also used to explore the over-expression pattern of H2A.L.1 isoforms in a mouse model of male infertility. CONCLUSIONSOur results demonstrate that targeted proteomics is a powerful method to quantify highly similar histone variants and isoforms. The developed method can be easily transposed to the study of human histone variants, whose abundance can be deregulated in various diseases.
ISSN:1756-8935
1756-8935
DOI:10.1186/s13072-017-0172-y