Circadian clock-independent ultradian rhythms in lipid metabolism in the Drosophila fat body.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Blanca Lago Solis,Rafael Koch,Emi Nagoshi
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引用次数: 0

Abstract

The role of circadian clocks in regulating metabolic processes is well known; however, their impact on metabolic states across species and life stages remains largely unexplored. This study investigates the relationship between circadian rhythms and metabolic regulation in the Drosophila larval fat body, a metabolic hub analogous to the mammalian liver and adipose tissue. Surprisingly, the fat body of period null mutants, which lack a functional circadian clock in all tissues, exhibited 12-hour rhythms in gene expression, particularly those involved in peroxisome function, lipid metabolism, and oxidative stress response. These transcriptomic rhythms were aligned with 12-hour oscillations in peroxisome biogenesis and activity, reactive oxygen species levels, and lipid peroxidation. Furthermore, period mutants exhibited 12-hour rhythms in body fat storage, ultimately leading to a net reduction in body fat levels. Collectively, our results identify clock-independent ultradian rhythms in lipid metabolism that are essential for larval survival and development.
果蝇脂肪体脂质代谢中不依赖生物钟的超昼夜节律。
生物钟在调节代谢过程中的作用是众所周知的;然而,它们对不同物种和生命阶段的代谢状态的影响在很大程度上仍未被探索。本研究探讨了果蝇幼虫脂肪体中昼夜节律与代谢调节之间的关系,脂肪体是类似于哺乳动物肝脏和脂肪组织的代谢中心。令人惊讶的是,无周期突变体的脂肪体,在所有组织中都缺乏功能性生物钟,在基因表达上表现出12小时的节律,特别是那些涉及过氧化物酶体功能、脂质代谢和氧化应激反应的基因。这些转录组节律与过氧化物酶体生物发生和活性、活性氧水平和脂质过氧化的12小时振荡一致。此外,周期突变体在体脂储存方面表现出12小时的节律,最终导致体脂水平的净减少。总的来说,我们的研究结果确定了脂质代谢中不依赖时钟的超昼夜节律,这对幼虫的生存和发育至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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