Integrating SNPs and STRPs in Population Genetics

将 SNP 和 STRP 整合到群体遗传学中

• 批准号: 7523320
• 负责人: Bret A Payseur
• 金额: $ 27.5万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-15 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7523320
• 关键词: Address; Biological Markers; Biology; Class; Classification; Complex; Computer Simulation; DNA; Development; Disease; Event; Evolution; Foundations; Genetic Polymorphism; Genetic Variation; Genome; Genomics; Goals; Human; Human Genome; Inherited; Joints; Link; Linkage Disequilibrium; Maps; Measures; Modeling; Mutate; Mutation; Outcome; Pattern; Performance; Population; Population Genetics; Process; Property; Rate; Recording of previous events; Research; Short Tandem Repeat Polymorphism; Single Nucleotide Polymorphism; Statistical Methods; Theoretical Studies; Variant; base; human disease; improved; insight; interest; trait

DESCRIPTION (provided by applicant): Patterns of variation at molecular markers provide exciting insights into the evolution of natural populations. Variation at the two most commonly used molecular markers, single nucleotide polymorphisms (SNPs) and short tandem repeat polymorphisms (STRPs), arises from different mutational processes, leading to complementary inferences about evolutionary forces. Because of higher mutation rates, STRPs better reveal recent evolutionary events, whereas slowly mutating SNPs are more powerfully applied to reconstructing older evolutionary events. Despite this crucial difference, patterns of polymorphism at SNPs and STRPs have rarely been compared directly in empirical or theoretical studies. The proposed research will address this important challenge by jointly examining genomic patterns of variation at SNPs and STRPs in human populations and by conducting computer simulations that explicitly model the contrasting mutational processes at the two marker classes. Specifically, this project will (1) compare expected patterns of polymorphism at SNPs, STRPs, and SNPs+STRPs generated under different evolutionary processes, (2) compare the performance of SNPs, STRPs, and SNPs+STRPs as markers for association studies of complex traits, (3) characterize expected linkage disequilibrium and other diversity correlations between linked SNPs and STRPs, and (4) measure patterns of co-variation between linked SNPs and STRPs across the human genome. This combined empirical and theoretical effort will yield the first systematic comparison of patterns of SNP and STRP polymorphism. Evolutionary scenarios that produce patterns of polymorphism that are relatively robust to variation in the STRP mutational model will be specifically sought as promising avenues for inference. Important outcomes of the proposed research include: objective guidance on marker choice based on timescale and evolutionary process of interest, a framework for integrating polymorphism at neighboring SNPs and STRPs throughout the human genome, and a foundation for the development of statistical methods that combine these two markers to enhance population genetic inference. By directly examining linkage disequilibrium between SNPs and STRPs across the human genome and quantitatively comparing the power of analyses using different or combined marker types, this research will also yield improved strategies for association mapping of complex human diseases. This project will examine the properties of different classes of human DNA variation. The results will help reveal the causes of the genetic variation that underlies complex inherited diseases. Project Relevance: This project will examine the properties of different classes of human DNA variation. The results will help reveal the causes of the genetic variation that underlies complex inherited diseases.

描述(由申请人提供)：分子标记的变异模式为自然种群的进化提供了令人兴奋的见解。单核苷酸多态(SNPs)和短串联重复序列多态(STRPs)这两个最常用的分子标记的变异来自不同的突变过程，导致对进化力量的互补推断。由于更高的突变率，STRP更好地揭示了最近的进化事件，而缓慢突变的SNP更适用于重建旧的进化事件。尽管存在这一关键差异，但在实证或理论研究中，很少有人直接比较SNPs和STRPs的多态模式。这项拟议的研究将通过联合检查人类群体中SNPs和STRP的基因组变异模式，并通过进行计算机模拟来明确地模拟这两个标记类别的对比突变过程，来解决这一重要挑战。具体地说，这个项目将(1)比较在不同进化过程中产生的SNPs、STRPs和SNPs+STRp的预期多态模式，(2)比较SNPs、STRp和SNPs+STRp作为复杂性状关联研究标记的表现，(3)描述连锁SNPs和STRPs之间预期的连锁不平衡和其他多样性相关性，以及(4)测量整个人类基因组中连锁SNPs和STRPs之间的协变模式。这项经验和理论相结合的工作将产生第一次对SNP和STRP多态模式的系统比较。产生对STRP突变模型中的变异相对稳健的多态模式的进化情景将被特别寻找作为有希望的推断途径。拟议研究的重要成果包括：基于时间尺度和感兴趣的进化过程的标记选择的客观指导，整合整个人类基因组中邻近SNP和STRP的多态的框架，以及开发结合这两个标记以增强群体遗传推断的统计方法的基础。通过直接检查人类基因组中SNPs和STRPs之间的连锁不平衡，并定量比较使用不同或组合标记类型的分析能力，这项研究还将为复杂人类疾病的关联图谱提供改进的策略。这个项目将研究不同类别的人类DNA变异的特性。这一结果将有助于揭示复杂遗传性疾病背后的遗传变异的原因。 项目相关性：该项目将检查不同类别的人类DNA变异的特性。这一结果将有助于揭示复杂遗传性疾病背后的遗传变异的原因。