Quantitative measurement of histone tail acetylation reveals stage-specific regulation and response to environmental changes during Drosophila development
Ryan A. Henry, Tanu Singh, Yin-Ming Kuo, Alison Biester, Abigail O’Keefe, Sandy Lee, Andrew J. Andrews, Alana M. O’Reilly and Janell L Mensinger
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.
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 Center
Tanu Singh - Drexel University
Yin-Ming Kuo - Fox Chase Cancer Center
Alison Biester - Fox Chase Cancer Center
Abigail O’Keefe - Fox Chase Cancer Center
Sandy Lee - Fox Chase Cancer Center
Andrew J. Andrews - Fox Chase Cancer Center
Alana M. O’Reilly - Fox Chase Cancer Center
Janell 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
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