Time makes histone H3 modifications drift in mouse liver

R. Hillje, L. Luzi, S. Amatori, Giuseppe Persico, F. Casciaro, Martina Rusin, M. Fanelli, P. Pelicci, M. Giorgio
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引用次数: 1

Abstract

To detect the epigenetic drift of time passing, we determined the genome-wide distributions of mono- and tri-methylated lysine 4 and acetylated and tri-methylated lysine 27 of histone H3 in the livers of healthy 3, 6 and 12 months old C57BL/6 mice. The comparison of different age profiles of histone H3 marks revealed global redistribution of histone H3 modifications with time, in particular in intergenic regions and near transcription start sites, as well as altered correlation between the profiles of different histone modifications. Moreover, feeding mice with caloric restriction diet, a treatment known to retard aging, reduced the extent of changes occurring during the first year of life in these genomic regions.
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时间使组蛋白H3修饰在小鼠肝脏中漂移
为了检测时间流逝的表观遗传漂变,我们测定了健康3、6和12月龄C57BL/6小鼠肝脏中组蛋白H3的单甲基化赖氨酸4和三甲基化赖氨酸4以及乙酰化和三甲基化赖氨酸27的全基因组分布。组蛋白H3标记的不同年龄谱的比较揭示了组蛋白H3修饰随着时间的推移在全球范围内重新分布,特别是在基因间区域和转录起始位点附近,以及不同组蛋白修饰谱之间的相关性改变。此外,给老鼠喂食热量限制饮食,一种已知的延缓衰老的治疗方法,减少了这些基因组区域在生命的第一年发生的变化的程度。
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