Enabling Precision Genomics Using Adaptive Variation

使用自适应变异实现精密基因组学

• 批准号: 10032497
• 负责人: RASMUS NIELSEN
• 金额: $ 43.51万
• 依托单位: UNIVERSITY OF CALIFORNIA BERKELEY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-08-01 至 2024-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10032497
• 关键词: Agriculture; Alleles; Biological Assay; CRISPR/Cas technology; Cell Line; Cells; Complex; Computer software; Computing Methodologies; DNA; DNA Sequence; Data; Diet; Differential Mortality; Diploid Cells; Disease; Environment; Europe; European; Evolution; Fatty Acids; Fertility; Genes; Genetic; Genetic Epistasis; Genetic Recombination; Genetic Variation; Genome; Genomics; Genotype; Graph; Haploid Cells; Heritability; Human; Human Cell Line; Human Genome; Immune; Individual; Infection; Infectious Agent; Likelihood Functions; Location; Maps; Mediating; Medical; Messenger RNA; Methods; Modeling; Mutation; Natural Selections; Nucleotides; Pathogenicity; Phenotype; Physiological; Population; Research Personnel; Site; Somatic Cell; Source; Statistical Methods; Statistical Models; System; Testing; Time; Variant; base; causal variant; cell type; fatty acid metabolism; fitness; gene environment interaction; genetic architecture; genetic variant; genome editing; genome wide association study; human DNA; human pluripotent stem cell; human stem cells; interest; new technology; pathogen; predictive modeling; protein metabolite; tool; trait

Project Summary Genes under natural selection may be related to heritable diseases, and variation in fitness more generally. For example, genetic variants related to differential mortality rates during pathogenic infections will be under natural selection when the infectious agents are present in the population. Inferences about selection at the genomic level in humans, therefore, provide a rich source of new testable hypotheses about functional relationships. However, while there are many methods for detecting natural selection at the genetic level, it is often very hard to determine exactly which genetic variants were targeted by selection. The aim of our study is to provide new computational methods for identifying causal mutations, and to apply these methods, in order to better understand the map between genotype and phenotype of loci that are, or have been, targeted by natural selection. We will apply the method to FADS genes, which harbor genetic variation associated with fatty acid metabolism and which have been under selection in European populations after the introduction of agriculture. We will test computational predictions experimentally in human cell lines modified using CRISPR/Cas9 technology. This will lead to a deeper understanding of the genetic differences among humans in these physiologically very important genes. In Aim 1 we will develop new computational methods that can infer, from DNA sequence data, which mutations have been targeted by natural selection. The methods will be able to incorporate the possibility that more than one mutation has been under selection and will also be able to leverage various forms of phenotypic and functional data. In Aim 2, we will test computational predictions regarding selection in the FADS genes using CRISPR/Cas9 in human cell lines. In addition to identifying the functional mutations, we will test hypotheses about interaction between mutations and between mutations and the environment, as represented by the distribution of fatty acids available to the cells in the substrate they are growing on. In Aim 3 we will extend the methods to be able to model selection in complex demographic models. We will also extend the method to be able to include environmental co-variates and ancient DNA. This will allow us to test hypotheses informed by the results of Aim 2 regarding the factors causing selection in the FADS genes.

项目摘要 自然选择下的基因可能与遗传性疾病有关，更广泛地说，与适应性的变化有关。 例如，与病原体感染期间不同死亡率相关的遗传变异将在 当传染源存在于种群中时的自然选择。关于选择的推论 因此，人类的基因组水平提供了关于功能的新的可检验的假说的丰富来源， 关系。然而，尽管有许多方法可以在基因水平上检测自然选择， 通常很难准确地确定哪些遗传变异是选择的目标。我们的目标是 研究的目的是提供新的计算方法来识别因果突变，并应用这些方法。 方法，为了更好地理解基因座的基因型和表型之间的映射，或具有 是自然选择的目标我们将把这种方法应用到FADS基因上， 与脂肪酸代谢相关的变异，并已在欧洲 农业引进后的人口。我们将在实验中测试计算预测， 使用CRISPR/Cas9技术修饰的人类细胞系。这将使我们更深入地了解 这些生理上非常重要的基因在人类中的遗传差异。 在目标1中，我们将开发新的计算方法，可以从DNA序列数据中推断， 突变是自然选择的目标。这些方法将能够结合这种可能性， 一个以上的突变已经被选择，也将能够利用各种形式的 表型和功能数据。 在目标2中，我们将使用CRISPR/Cas9测试关于FADS基因选择的计算预测。 在人类细胞系中。除了识别功能性突变，我们还将测试以下假设 突变之间以及突变与环境之间的相互作用，如 脂肪酸在细胞生长基质中的分布。 在目标3中，我们将扩展这些方法，使其能够在复杂的人口模型中进行模型选择。我们将 还扩展了该方法，使其能够包括环境协变量和古代DNA。这将使我们 检验目标2中关于FADS中导致选择的因素的假设 基因.