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饥饿促进雄性而非雌性小鼠肝脏中的组蛋白赖氨酸丁酰化。

Starvation promotes histone lysine butyrylation in the liver of male but not female mice.

机构信息

Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Gene. 2020 Jun 30;745:144647. doi: 10.1016/j.gene.2020.144647. Epub 2020 Apr 2.

Abstract

AIMS

Post-translational modifications (PTMs) of histones are regulated by the availability of their respective acyl-CoAs. Among these histone PTMs, the metabolic origin of histone butyrylation (Kbu) is still poorly understood.

MATERIAL AND METHODS

The impact of starvation on the levels of Kbu was determined by western blotting on histones extracted from the liver of fed and fasted C57BL/6 mice and immunohistochemistry on liver paraffin sections.

KEY FINDINGS

Using animal model we provide evidence that the stimulation of ketogenesis following starvation, in addition to histone beta-hydroxybutyrylation (Kbhb), also leads to an increase in histone butyrylation (Kbu). Using an immunohistochemistry (IHC) approach we report first that hepatocytes contained butyrylated histones with important cell-to-cell heterogeneity. More importantly, our investigations based on western blotting and IHC also proposed that the basal levels of Kbu differ between male and female mice, with female mouse hepatocytes containing higher levels of butyrylated histones. Starvation enhanced solely histone Kbu levels in the liver of males but not females.

SIGNIFICANCE

This is the first demonstration of a sex-dependent large-scale stimulation of histone acylation. Our data also point to different basal metabolic conditions of the male and female liver cells with a sex-dependent impact on the hepatocytes' epigenome.

摘要

目的

组蛋白的翻译后修饰(PTMs)受其相应酰基辅酶 A 的可用性调节。在这些组蛋白 PTM 中,组蛋白丁酰化(Kbu)的代谢来源仍知之甚少。

材料和方法

通过对喂食和禁食 C57BL/6 小鼠肝脏中提取的组蛋白进行 Western 印迹和肝脏石蜡切片的免疫组织化学检测,确定饥饿对 Kbu 水平的影响。

主要发现

使用动物模型,我们提供了证据表明,饥饿后酮体生成的刺激除了导致组蛋白β-羟丁酰化(Kbhb)增加外,还导致组蛋白丁酰化(Kbu)增加。我们采用免疫组织化学(IHC)方法首次报道了肝细胞中含有具有重要细胞间异质性的丁酰化组蛋白。更重要的是,我们基于 Western 印迹和 IHC 的研究还提出,Kbu 的基础水平在雄性和雌性小鼠之间存在差异,雌性小鼠肝细胞中含有更高水平的丁酰化组蛋白。饥饿仅增强雄性而非雌性肝脏中组蛋白 Kbu 的水平。

意义

这是首次证明性别依赖性大规模刺激组蛋白酰化。我们的数据还指出了雄性和雌性肝细胞核的不同基础代谢条件,对肝细胞的表观基因组有性别依赖性影响。

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