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利用果蝇营养基因组学鉴定遗传性代谢紊乱的潜在饮食疗法。

Identifying potential dietary treatments for inherited metabolic disorders using Drosophila nutrigenomics.

机构信息

School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia.

Department of Physiology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.

出版信息

Cell Rep. 2024 Mar 26;43(3):113861. doi: 10.1016/j.celrep.2024.113861. Epub 2024 Feb 27.

Abstract

Inherited metabolic disorders are a group of genetic conditions that can cause severe neurological impairment and child mortality. Uniquely, these disorders respond to dietary treatment; however, this option remains largely unexplored because of low disorder prevalence and the lack of a suitable paradigm for testing diets. Here, we screened 35 Drosophila amino acid disorder models for disease-diet interactions and found 26 with diet-altered development and/or survival. Using a targeted multi-nutrient array, we examine the interaction in a model of isolated sulfite oxidase deficiency, an infant-lethal disorder. We show that dietary cysteine depletion normalizes their metabolic profile and rescues development, neurophysiology, behavior, and lifelong fly survival, thus providing a basis for further study into the pathogenic mechanisms involved in this disorder. Our work highlights the diet-sensitive nature of metabolic disorders and establishes Drosophila as a valuable tool for nutrigenomic studies for informing potential dietary therapies.

摘要

遗传性代谢紊乱是一组遗传疾病,可导致严重的神经损伤和儿童死亡。这些疾病的独特之处在于它们对饮食治疗有反应;然而,由于疾病的患病率低,以及缺乏合适的饮食测试模式,这种选择在很大程度上仍未得到探索。在这里,我们筛选了 35 种果蝇氨基酸代谢紊乱模型,以研究疾病与饮食的相互作用,发现其中 26 种模型的发育和/或存活受到饮食的影响。我们使用靶向多营养数组,在亚硫酸氧化酶缺乏症(一种婴儿致死性疾病)的模型中研究了这种相互作用。我们发现,饮食中半胱氨酸的消耗可以使它们的代谢谱正常化,并挽救其发育、神经生理学、行为和终生的果蝇存活,从而为进一步研究该疾病相关的致病机制提供了基础。我们的工作强调了代谢紊乱的饮食敏感性,并确立了果蝇作为营养基因组学研究的有价值工具,为潜在的饮食治疗提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc1a/11037929/b37780021303/nihms-1980915-f0002.jpg

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