Cigarette Smoke Component Acrolein Modulates Chromatin Assembly by Inhibiting Histone Acetylation

被引:62
作者
Chen, Danqi
Fang, Lei
Li, Hongjie
Tang, Moon-shong
Jin, Chunyuan
机构
[1] NYU, Sch Med, Dept Environm Med, New York, NY 10987 USA
[2] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10987 USA
基金
美国国家卫生研究院;
关键词
Cigarette Smoke; Epigenetics; Histone Modification; Nucleosome; Transcription; Acrolein; Chromatin Assembly; LUNG-CANCER; TRANSCRIPTIONAL RESPONSES; MUTATIONAL HOTSPOTS; GENE-EXPRESSION; DNA-DAMAGE; CELL-CYCLE; REPLICATION; VARIANTS; BINDING; ACTIVATION;
D O I
10.1074/jbc.M113.476630
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 ,-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.
引用
收藏
页码:21678 / 21687
页数:10
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