生长期饮食降低组蛋白乙酰转移酶Gcn5功能,缩短雄性果蝇寿命。

IF 6.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shoko Mizutani, Kanji Furuya, Ayumi Mure, Yuuki Takahashi, Akihiro Mori, Nozomu Sakurai, Takuto Suito, Kohjiro Nagao, Masato Umeda, Kaori Watanabe, Yukako Hattori, Tadashi Uemura
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引用次数: 0

摘要

生命早期的营养环境,即营养史,对发育阶段之外的健康有着深远的影响。在这里,我们以黑腹果蝇(Drosophila melanogaster)为模型,用含有多种酵母突变体的饲料喂养幼虫,并探索由此产生的影响成年果蝇寿命的历史。由酵母nat3ko组成的幼虫饮食缩短了雄性成虫的寿命;显著降低了组蛋白乙酰转移酶Gcn5在幼虫体内的功能。与此同时,gcn5介导的幼虫全身或神经元基因调控的扰动显著促进了成虫的早期死亡。nat3ko饲粮中长链脂肪酸和支链氨基酸(BCAAs)含量远高于对照酵母饲粮。在对照日粮中添加油酸、缬氨酸和乙酸,重现了nat3 KO日粮对幼虫转录组和雄性寿命的影响。我们的研究结果强烈表明,在发育阶段富含脂肪酸和支链氨基酸的饮食与通过对Gcn5功能的不利影响而缩短寿命之间存在因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Growth phase diets diminish histone acetyltransferase Gcn5 function and shorten lifespan of Drosophila males.

The nutritional environment in early life, referred to as the nutrition history, exerts far-reaching health effects beyond the developmental stage. Here, with Drosophila melanogaster as a model, we fed larvae on diets consisting of a variety of yeast mutants and explored the resulting histories that impacted adult lifespan. A larval diet comprised of yeast nat3 KO shortened the lifespan of male adults; and remarkably, this diet diminished the function of histone acetyltransferase Gcn5 in larvae. Concordantly, perturbation of Gcn5-mediated gene regulation in the larval whole body or neurons significantly contributed to the earlier death of adults. The nat3 KO diet is much more abundant in long-chain fatty acids and branched-chain amino acids (BCAAs) than the control yeast diet. Supplementing the control diet with a combination of oleic acid, valine, and acetic acid recapitulated the effects of the nat3 KO diet on the larval transcriptome and the lifespan of males. Our findings strongly suggest a causal link between a fatty acids- and BCAA-rich diet in developmental stages and lifespan reduction via the adverse effect on the Gcn5 function.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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