Journal article
Quantitative measurement of histone tail acetylation reveals stage-specific regulation and response to environmental changes during Drosophila development
Biochemistry (Easton), v 55(11), pp 1663-1672
18 Feb 2016
PMID: 26836402
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Histone modification plays a major role in regulating gene transcription and ensuring the healthy development of an organism. Numerous studies have suggested that histones are dynamically modified during developmental events to control gene expression levels in a temporal and spatial manner. However, the study of histone acetylation dynamics using currently available techniques is hindered by the difficulty of simultaneously measuring acetylation of the numerous potential sites of modification present in histones. Here, we present a methodology that allows us to combine mass spectrometry-based histone analysis with
Drosophila
developmental genetics. Using this system, we characterized histone acetylation patterns during multiple developmental stages of the fly. Additionally, we utilized this analysis to characterize how treatments with pharmacological agents or environmental changes such as gamma-irradiation altered histone acetylation patterns. Strikingly, gamma-irradiation dramatically increased acetylation at H3K18, a site linked to DNA repair via non-homologous end joining. In mutant fly strains deficient in DNA repair proteins, however, this increase in H3K18 acetylation was lost. These results demonstrate the efficacy of our combined mass spectrometry system with a
Drosophila
model system, and provide interesting insight into the changes in histone acetylation during development, as well as the effects of both pharmacological and environmental agents on global histone acetylation.
Metrics
Details
- Title
- Quantitative measurement of histone tail acetylation reveals stage-specific regulation and response to environmental changes during Drosophila development
- Creators
- Ryan A. Henry - Fox Chase Cancer CenterTanu Singh - Drexel UniversityYin-Ming Kuo - Fox Chase Cancer CenterAlison Biester - Fox Chase Cancer CenterAbigail O’Keefe - Fox Chase Cancer CenterSandy Lee - Fox Chase Cancer CenterAndrew J. Andrews - Fox Chase Cancer CenterAlana M. O’Reilly - Fox Chase Cancer CenterJanell L Mensinger
- Publication Details
- Biochemistry (Easton), v 55(11), pp 1663-1672
- Publisher
- American Chemical Society; Washington, DC
- Resource Type
- Journal article
- Language
- English
- Web of Science ID
- WOS:000372856400011
- Scopus ID
- 2-s2.0-84962128854
- Other Identifier
- 991019357636604721
UN Sustainable Development Goals (SDGs)
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Biochemistry & Molecular Biology