Altered macronutrient composition and genetics influence the complex transcriptional network associated with adiposity in the Collaborative Cross.

Phoebe Yam, Melissa VerHague, Jody Albright, Erik Gertz, Fernando Pardo-Manuel de Villena, Brian J Bennett
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引用次数: 1

Abstract

Background: Obesity is a serious disease with a complex etiology characterized by overaccumulation of adiposity resulting in detrimental health outcomes. Given the liver's critical role in the biological processes that attenuate adiposity accumulation, elucidating the influence of genetics and dietary patterns on hepatic gene expression is fundamental for improving methods of obesity prevention and treatment. To determine how genetics and diet impact obesity development, mice from 22 strains of the genetically diverse recombinant inbred Collaborative Cross (CC) mouse panel were challenged to either a high-protein or high-fat high-sucrose diet, followed by extensive phenotyping and analysis of hepatic gene expression.

Results: Over 1000 genes differentially expressed by perturbed dietary macronutrient composition were enriched for biological processes related to metabolic pathways. Additionally, over 9000 genes were differentially expressed by strain and enriched for biological process involved in cell adhesion and signaling. Weighted gene co-expression network analysis identified multiple gene clusters (modules) associated with body fat % whose average expression levels were influenced by both dietary macronutrient composition and genetics. Each module was enriched for distinct types of biological functions.

Conclusions: Genetic background affected hepatic gene expression in the CC overall, but diet macronutrient differences also altered expression of a specific subset of genes. Changes in macronutrient composition altered gene expression related to metabolic processes, while genetic background heavily influenced a broad range of cellular functions and processes irrespective of adiposity. Understanding the individual role of macronutrient composition, genetics, and their interaction is critical to developing therapeutic strategies and policy recommendations for precision nutrition.

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改变宏量营养素组成和遗传影响与肥胖相关的复杂转录网络在协作杂交。
背景:肥胖是一种病因复杂的严重疾病,其特征是脂肪的过度积累导致有害的健康结果。鉴于肝脏在减轻肥胖积累的生物过程中发挥着关键作用,阐明遗传和饮食模式对肝脏基因表达的影响是改善肥胖预防和治疗方法的基础。为了确定遗传和饮食如何影响肥胖的发展,研究人员对22个基因多样化重组近交系协作杂交(CC)小鼠小组中的小鼠进行了高蛋白或高脂肪高蔗糖饮食的挑战,然后进行了广泛的表型分析和肝脏基因表达分析。结果:1000多个因膳食宏量营养素组成紊乱而差异表达的基因富集于与代谢途径相关的生物过程中。此外,菌株差异表达了9000多个基因,并富集了参与细胞粘附和信号传导的生物过程。加权基因共表达网络分析确定了与体脂%相关的多个基因簇(模块),其平均表达水平受饮食宏量营养素组成和遗传的影响。每个模块都丰富了不同类型的生物功能。结论:遗传背景总体上影响CC的肝脏基因表达,但饮食宏量营养素的差异也改变了特定基因子集的表达。宏量营养素组成的变化改变了与代谢过程相关的基因表达,而遗传背景严重影响了与肥胖无关的广泛的细胞功能和过程。了解宏量营养素组成、遗传学及其相互作用的个体作用对于制定精准营养的治疗策略和政策建议至关重要。
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