QTL and QTL Genes Underlying Lactation Performance

QTL 和影响泌乳性能的 QTL 基因

• 批准号: 7660129
• 负责人: DARRYL L HADSELL
• 金额: $ 20.44万
• 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: 2009-04-10 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7660129
• 关键词: Academy; Accounting; Age-Months; American; Biological; Breast Feeding; Cattle; Cell Respiration; Chromosome Mapping; Collection; Computer Simulation; Computing Methodologies; Coupled; Data; Databases; Development; Fostering; Functional disorder; Gene Expression; Genes; Genetic; Genome; Genomics; Genotype; Goals; Growth and Development function; Haplotypes; Health; Healthcare; Homologous Gene; Human; Human Genome; Inbred Strains Mice; Infant; Laboratories; Lactation; Link; Location; Mammals; Mammary gland; Maps; Maternal Behavior; Measurement; Measures; Milk; Mitochondria; Mouse Strains; Mus; Outcome; Pathway interactions; Pediatrics; Performance; Phenotype; Physiological; Physiology; Play; Production; Publishing; Quantitative Trait Loci; Recommendation; Relative (related person); Resources; Role; Scanning; Sequence Analysis; Single Nucleotide Polymorphism; Staging; Tissues; United States; Variant; Woman; autosome; base; cost effective; genome sequencing; mammary gland development; novel; public health relevance; research study; success; therapeutic target; tool; trait

DESCRIPTION (provided by applicant): Breastfeeding is now widely accepted as important to optimizing health, growth and development of humans and reducing the financial burden for health care in the United States. The current recommendation by the American Academy of Pediatrics is that infants be exclusively breast fed to 6 months of age. Today, most women who choose to breast feed have difficulty maintaining a productive lactation for that long. The most common reason cited for early cessation of breastfeeding is insufficient milk volume. Biological, physiological and even familial factors probably all play a role in determining lactation outcome. To understand this critical variability between women, an understanding of the mechanisms regulating lactation is crucial. In other mammals such as the cow and the mouse milk production is a heritable trait. Despite these findings, however, the genes that contribute to milk production are largely unidentified. In the bovine, there are quantitative trait loci (QTL) for milk volume present on all 29 autosomes. Only a few of the genes underlying these QTL have been identified. In the mouse, even fewer QTL have been published. None of the current mouse QTL studies have published data on milk production during lactogenesis II, milk composition, or mammary gland development, factors that are all important to lactational success in breastfeeding women. Our laboratory uses litter-crossfostering approaches to measure relative milk production in the mouse. These approaches have allowed for indirect measurement of relative milk production capacity during all stages of the cycle with a degree of increased sensitivity and precision that has not been present in previous studies. We have also measured milk composition, mammary gland mitochondrial function and maternal behavior, and conducted extensive analysis of mammary gland development and gene expression over the course of the lactation cycle. These preliminary studies demonstrate that mammary tissue oxidative metabolism is temporally linked to milk production The hypothesis of this proposal is that phenotypic variation in milk production-associated traits among mouse strains will be accounted for by differences in mammary tissue oxidative metabolism and will be linked to QTL identified through in-silico association mapping. Our cross-fostering paradigm will be used to isolate and measure maternal phenotypic differences in important lactation-related traits among a collection of inbred mouse strains known as the mouse diversity panel. We will then determined if these differences are associated with altered mammary mitochondrial function and then conduct In-silico whole genome association scans to identify the QTL linked to these lactation performance and mitochondrial function traits. These QTL will be mapped onto the human Hapmap and serve as the basis for a subsequent RO1 aimed at identifying genes and gene-expression pathways which determine lactation performance in breastfeeding women. PUBLIC HEALTH RELEVANCE: Breastfeeding is now widely accepted as important to optimizing health, growth and development of humans and reducing the financial burden for health care on the United States. The current recommendation by the American Academy of Pediatrics is that infants be exclusively breast fed to 6 months of age. Today, most women who choose to breast feed have difficulty maintaining a productive lactation for that long. The experiments described in this proposal will use powerful new mouse genetic tools to identify and map the genes which could regulate lactation outcomes in breastfeeding women.

描述(申请人提供)：在美国，母乳喂养现在被广泛认为是优化人类健康、成长和发展以及减轻医疗保健经济负担的重要因素。美国儿科学会目前的建议是，6个月大的婴儿应该全母乳喂养。今天，大多数选择母乳喂养的女性很难维持那么长时间的高效哺乳。提早停止母乳喂养的最常见原因是奶量不足。生物、生理甚至家庭因素都可能在决定哺乳结局中发挥作用。要了解女性之间的这种关键差异，了解调节哺乳的机制是至关重要的。在其他哺乳动物中，如牛和老鼠，产奶是一种可遗传的特征。然而，尽管有这些发现，影响产奶量的基因在很大程度上是未知的。在牛中，所有29个常染色体上都存在控制乳量的数量性状基因座(QTL)。目前只发现了这些QTL背后的几个基因。在小鼠身上，发表的QTL甚至更少。目前没有一项小鼠QTL研究公布了第二次泌乳过程中的产奶量、牛奶成分或乳腺发育的数据，这些因素对哺乳妇女的哺乳成功都很重要。我们的实验室使用产仔杂交的方法来测量小鼠的相对产奶量。这些方法使得能够间接测量周期所有阶段的相对牛奶生产能力，提高了灵敏度和精确度，这在以前的研究中是没有的。我们还测量了牛奶成分、乳腺线粒体功能和母体行为，并对乳腺发育和哺乳周期中的基因表达进行了广泛的分析。这些初步研究表明，乳房组织氧化代谢与产奶量在时间上是相关的。这一建议的假设是，小鼠品系之间产奶量相关性状的表型差异将由乳房组织氧化代谢的差异来解释，并将与通过电子关联作图确定的QTL连锁。我们的交叉培养模式将被用来分离和测量近交系小鼠中与哺乳相关的重要性状的母体表型差异，这一集合被称为小鼠多样性小组。然后，我们将确定这些差异是否与乳腺线粒体功能改变有关，然后进行电子全基因组关联扫描，以确定与这些哺乳性能和线粒体功能特征相关联的QTL。这些QTL将被映射到人类HapMap上，并作为后续RO1的基础，旨在识别决定哺乳妇女哺乳性能的基因和基因表达途径。与公共健康相关：母乳喂养现在被广泛认为是优化人类健康、生长和发展以及减轻美国医疗保健财政负担的重要因素。美国儿科学会目前的建议是，6个月大的婴儿应该全母乳喂养。今天，大多数选择母乳喂养的女性很难维持那么长时间的高效哺乳。这项提案中描述的实验将使用强大的新老鼠基因工具来识别和绘制可能调节哺乳妇女哺乳结果的基因。