Functional genetic evolution of human brain and behavior

人脑和行为的功能遗传进化

• 批准号: 8702035
• 负责人: Eric J. Vallender
• 金额: $ 3.3万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-08-10 至 2014-11-01
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8702035
• 关键词: 3' Untranslated Regions; 5' Untranslated Regions; Adolescent; Affect; Alcoholism; Alcohols; Animal Disease Models; Animal Model; Anxiety; Autistic Disorder; Behavior; Brain; Candidate Disease Gene; Cataloging; Catalogs; Catecholamines; Cercopithecidae; Cerebrospinal Fluid; Code; Corticotropin; Development; Disease; Dissociation; Enhancers; Frequencies; Funding; Gene Expression; Gene Proteins; Genes; Genetic; Genetic Models; Genetic Polymorphism; Genotype; Goals; Gonadal Steroid Hormones; Grant; Haplotypes; Homeostasis; Human; Hydrocortisone; In Vitro; Incidence; Lead; Macaca mulatta; Measurement; Measures; Mental Depression; Mental disorders; Messenger RNA; Modeling; Molecular Evolution; Monkeys; Monoamine Oxidase; Monoamine Oxidase A; Mutation; Naltrexone; Neurobiology; Neurosciences; Neurosecretory Systems; Organism; Pan Genus; Pharmaceutical Preparations; Pharmacogenetics; Phenotype; Physiological; Plasma; Pongidae; Primates; Reporter; Research Personnel; Scientist; Self Administration; Self-Administered; Serotonin; Substance abuse problem; Symptoms; Testing; Untranslated Regions; Variant; Work; addiction; alcohol use disorder; base; behavior measurement; brain behavior; comparative; early-onset alcoholism; expression vector; genetic evolution; human disease; in vivo; monoamine; neurochemistry; neuropsychiatry; nonhuman primate; promoter; protein function; public health relevance; species difference; vector

DESCRIPTION (provided by applicant): This proposal is focused on integrating comparative genetics and molecular evolution with functional neurobiology as a means of generating a better understanding of human neuropsychiatric and addiction disorders and developing better animal disease models. This will concentrate initially on monoamine oxidase A (MAOA). MAOA has been associated with neuropsychiatric and addiction disorders including alcoholism, depression, and autism among others and is a target for widely prescribed anti-depression and anti-anxiety medications. MAOA is also hypothesized to have undergone positive selection in humans since the divergence from chimpanzees but harbors a regulatory polymorphism that is functionally homologous between humans, apes, and certain old-world monkey species. Understanding differences in MAOA function in humans may lead to better understandings of the causes of its associated neuropsychiatric disorders and allow for the development of more appropriate genetic models of these diseases in non-human primates. Here we propose to catalog the complete MAOA locus across primate species, including polymorphic variation in the more commonly used biomedical model species. We then propose to functionally investigate the consequences of these differences, as well as the functionality of ancestral sequences, in vitro. We will also assess the effects of polymorphic variation from non-human primates ex vivo and in vivo through measurement of mRNA levels and neurochemical concentrations in cerebrospinal fluid and neuroendocrine effects in blood plasma. Finally, we will integrate MAOA genotypes into existing alcohol self-administration studies in rhesus macaques to elucidate this genotype/phenotype relationship and develop better genetic models of alcohol use disorders. Through this work, a better understanding will be gained of the relevance of molecular evolution and comparative genetics to functional neuroscience and the study of human neuropsychiatric disease. Specifically, this work will elucidate if specific psychiatric disorders or symptoms are unique to humans resulting from human-specific genetic changes and the extent to which and ways that these psychiatric disorders and their treatment can be modeled in other organisms, particularly non-human primates. This will allow a better integration of the two fields and allow researchers to leverage the power of molecular evolution and comparative genetics to greater effect in studies of human disease going forward. It will also allow scientists to refine candidate gene analyses and better place into context animal models of neuropsychiatric disease. PUBLIC HEALTH RELEVANCE: The goal of this grant is to understand the functional genetic differences between humans and other primates at the monoamine oxidase a gene and to use this information to understand human neurobiology and behavior. We will identify the differences among primate species and test these differences for functional effects of gene expression and protein function before considering how they affect behaviors and neurochemical levels in the body. This work will allow us to better understand how the human brain works, what goes wrong in neuropsychiatric disorders and ways in which we might develop better animal models for studying human disease.

描述（由申请人提供）：该提案的重点是将比较遗传学和分子进化与功能神经生物学相结合，作为更好地了解人类神经精神和成瘾疾病并开发更好的动物疾病模型的手段。这将首先集中于单胺氧化酶 A (MAOA)。 MAOA 与神经精神疾病和成瘾疾病有关，包括酗酒、抑郁症和自闭症等，并且是广泛使用的抗抑郁和抗焦虑药物的目标。还假设 MAOA 自与黑猩猩分化以来在人类中经历了正选择，但具有在人类、猿和某些旧世界猴物种之间功能同源的调节多态性。了解人类 MAOA 功能的差异可能会导致更好地了解其相关神经精神疾病的原因，并允许在非人类灵长类动物中开发这些疾病的更合适的遗传模型。在这里，我们建议对灵长类动物物种的完整 MAOA 基因座进行编目，包括更常用的生物医学模型物种中的多态性变异。然后，我们建议在体外对这些差异的后果以及祖先序列的功能进行功能研究。我们还将通过测量脑脊液中的 mRNA 水平和神经化学物质浓度以及血浆中的神经内分泌效应来评估非人灵长类动物离体和体内多态性变异的影响。最后，我们将把 MAOA 基因型整合到现有的恒河猴酒精自我管理研究中，以阐明这种基因型/表型关系，并开发更好的酒精使用障碍遗传模型。通过这项工作，将更好地了解分子进化和比较遗传学与功能神经科学和人类神经精神疾病研究的相关性。具体来说，这项工作将阐明特定的精神疾病或症状是否是人类独有的，是由人类特有的基因变化引起的，以及这些精神疾病及其治疗的程度和方式可以在其他生物体，特别是非人类灵长类动物中建模。这将使这两个领域更好地融合，并使研究人员能够利用分子进化和比较遗传学的力量，在未来的人类疾病研究中发挥更大的作用。它还将使科学家能够完善候选基因分析，并更好地融入神经精神疾病的动物模型中。 公共健康相关性：这笔赠款的目的是了解人类和其他灵长类动物之间单胺氧化酶 a 基因的功能遗传差异，并利用这些信息来了解人类神经生物学和行为。我们将确定灵长类动物物种之间的差异，并测试这些差异对基因表达和蛋白质功能的功能影响，然后再考虑它们如何影响体内的行为和神经化学水平。这项工作将使我们能够更好地了解人类大脑的工作原理、神经精神疾病出了什么问题，以及我们如何开发更好的动物模型来研究人类疾病。