Epigenetic mechanisms in obesity

肥胖的表观遗传机制

• 批准号: 7998396
• 负责人: ROBERT A WATERLAND
• 金额: $ 4.46万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-12-21 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7998396
• 关键词: Adult; Affect; Age; Animal Model; Birth; Body Weight; Candidate Disease Gene; DNA Methylation; Developed Countries; Development; Diet; Environment; Epigenetic Process; Etiology; Female of child bearing age; Figs - dietary; Food Intake Regulation; Fostering; Gene Expression; Gene Expression Regulation; Genes; Genetic Predisposition to Disease; Genetic Variation; Human; Hypothalamic structure; Individual; Lactation; Leptin; Measurement; Measures; Melanocortin 4 Receptor; Methylation; Modeling; Mus; Mutation; Obesity; Pathway interactions; Pattern; Pregnancy; Prevalence; Regulation; Relative (related person); Research; Severities; Site; Specificity; Staging; Stimulus; Testing; Tissues; Variant; Weaning; Weight Gain; bisulfite; design; effective intervention; energy balance; epigenetic variation; fetal; gene function; genome-wide; mouse model; nutrition; offspring; postnatal; prenatal; prevent; public health relevance; trend

DESCRIPTION (provided by applicant): Obesity prevalence in the US and other developed countries has increased dramatically in recent decades. This trend is affecting individuals at every age, including women of child- bearing age. A major concern is that maternal obesity during pregnancy may alter the intrauterine environmental and thereby perpetuate obesity in her offspring. The viable yellow agouti (Avy) mouse is an ideal model in which to explore the effects of maternal obesity and diet on offspring body weight. Avy/a mice are spontaneously hyperphagic and develop adult-onset obesity. Severity of obesity, however, is highly variable among isogenic Avy/a mice. The overall hypothesis of the proposed research is that maternal obesity during pregnancy and/or lactation affects the establishment of gene-specific DNA methylation patterns in the developing hypothalamus, causing permanent changes in hypothalamic gene expression, food intake regulation, and body weight. The specific aims of this project are to: 1) characterize the developmental establishment and tissue-specificity of DNA methylation at hypothalamic genes that affect food intake regulation, 2) in the Avy mouse model, determine if the effects of maternal obesity on offspring body weight occur during prenatal or early postnatal development, and 3) determine if methylation and expression of specific genes in the hypothalamus of adult Avy/a mice are correlated with obesity. This research in animal models is necessary to elucidate the mechanisms by which maternal obesity affects offspring body weight; this information will enable us to accurately gauge the impact of such phenomena on the etiology of human obesity and potentially design effective interventions. PUBLIC HEALTH RELEVANCE: The overall hypothesis of the proposed research is that maternal obesity during pregnancy and/or lactation affects the establishment of gene-specific DNA methylation patterns in the developing hypothalamus, causing permanent changes in hypothalamic gene expression, food intake regulation, and body weight. We will investigate this hypothesis in mice with and without a genetic predisposition to obesity. Our results will elucidate the mechanisms by which maternal obesity affects offspring body weight, enabling us to accurately gauge the impact of such phenomena on the etiology of human obesity and, eventually, design effective interventions.

描述（由申请人提供）：近几十年来，美国和其他发达国家的肥胖率急剧上升。这一趋势正在影响各个年龄段的个人，包括育龄妇女。一个主要的担忧是，母亲怀孕期间的肥胖可能会改变子宫内的环境，从而使后代长期肥胖。可存活的黄色刺豚鼠 (Avy) 小鼠是探索母亲肥胖和饮食对后代体重影响的理想模型。 Avy/a 小鼠自发性食欲亢进并发展成成年肥胖。然而，同基因 Avy/a 小鼠的肥胖严重程度差异很大。拟议研究的总体假设是，怀孕和/或哺乳期间的母亲肥胖会影响发育中的下丘脑中基因特异性 DNA 甲基化模式的建立，导致下丘脑基因表达、食物摄入调节和体重的永久性变化。该项目的具体目标是：1) 表征影响食物摄入调节的下丘脑基因 DNA 甲基化的发育建立和组织特异性，2) 在 Avy 小鼠模型中，确定母亲肥胖是否对后代体重产生影响发生在产前或产后早期发育期间，3) 确定成年 Avy/a 小鼠下丘脑中特定基因的甲基化和表达是否与肥胖相关。这项动物模型研究对于阐明母亲肥胖影响后代体重的机制是必要的。这些信息将使我们能够准确评估此类现象对人类肥胖病因学的影响，并有可能设计出有效的干预措施。公共健康相关性：拟议研究的总体假设是，妊娠期和/或哺乳期母亲肥胖会影响发育中的下丘脑中基因特异性 DNA 甲基化模式的建立，导致下丘脑基因表达、食物摄入调节和身体的永久性变化。重量。我们将在具有和不具有肥胖遗传倾向的小鼠中研究这一假设。我们的研究结果将阐明母亲肥胖影响后代体重的机制，使我们能够准确衡量此类现象对人类肥胖病因的影响，并最终设计有效的干预措施。