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Cigarette Smoke Component Acrolein Modulates Chromatin Assembly by Inhibiting Histone Acetylation
Chromatin structure and gene expression are both regulated by nucleosome assembly. How environmental factors influence histone nuclear import and the nucleosome assembly pathway, leading to changes in chromatin organization and transcription, remains unknown. Acrolein (Acr) is an α,β-unsaturated ald...
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Published in: | The Journal of biological chemistry 2013-07, Vol.288 (30), p.21678-21687 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Chromatin structure and gene expression are both regulated by nucleosome assembly. How environmental factors influence histone nuclear import and the nucleosome assembly pathway, leading to changes in chromatin organization and transcription, remains unknown. Acrolein (Acr) is an α,β-unsaturated aldehyde, which is abundant in the environment, especially in cigarette smoke. It has recently been implicated as a potential major carcinogen of smoking-related lung cancer. Here we show that Acr forms adducts with histone proteins in vitro and in vivo and preferentially reacts with free histones rather than with nucleosomal histones. Cellular fractionation analyses reveal that Acr exposure specifically inhibits acetylations of N-terminal tails of cytosolic histones H3 and H4, modifications that are important for nuclear import and chromatin assembly. Notably, Acr exposure compromises the delivery of histone H3 into chromatin and increases chromatin accessibility. Moreover, changes in nucleosome occupancy at several genomic loci are correlated with transcriptional responses to Acr exposure. Our data provide new insights into mechanisms whereby environmental factors interact with the genome and influence genome function.
Background: The epigenetic effect of acrolein, an α,β-unsaturated aldehyde, remains unclear.
Results: Acrolein specifically inhibits acetylations of N-terminal tails of cytosolic but not nuclear histones and reduces their delivery into chromatin.
Conclusion: Acrolein differentially affects post-translational modifications of free histones and nucleosomal histones and compromises chromatin assembly.
Significance: Affecting chromatin assembly may represent a new model for the interaction between environmental factors and the genome function. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M113.476630 |