GENETIC DISSECTION OF AGGRESSIVE BEHAVIORS

攻击性行为的基因剖析

• 批准号: 6675250
• 负责人: EDWARD S BRODKIN
• 金额: $ 17.96万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-01 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6675250
• 关键词: aggression; behavioral /social science research tag; behavioral genetics; gene mutation; genetic mapping; genetic polymorphism; laboratory mouse; quantitative trait loci

DESCRIPTION (provided by applicant): This proposal seeks to provide Edward S. Brodkin, M.D. with a five-year period of supervised research training that will enable him to become an independent investigator, with a research focus on the genetic dissection of aggressive behaviors in mice. The candidate will gain training and experience in high resolution genetic mapping of quantitative trait loci (QTLs), candidate gene analysis, and mutagenesis methods. Background: Aggressive behaviors are a major source of morbidity and mortality in patients with severe neuropsychiatric disorders. A propensity towards aggression is substantially heritable in mammals. Genetic dissections of aggressive behaviors in mice can identify biological pathways that underlie mammalian aggression and that may be involved in the pathophysiology of human psychiatric disorders. Dr. Brodkin has previously identified aggression QTLs on chromosome 10 (Aggr1) and chromosome X (Aggr2) in NZB/B1NJ and A/J mice; however he has had no previous experience with high-resolution (fine) mapping of QTLs, candidate gene analysis, or mutagenesis methodologies. Training in these methodologies is important for the candidate's career development and is necessary for his future research independence. Specific Aims of Research Plan: 1. Fine-mapping aggression QTLs. Using NZB/B1NJ and AJ mice as progenitor strains, interval-specific congenic strains will be bred for the Aggr1 and Aggr2 QTL intervals and will be used to fine map the QTL intervals. 2. Candidate gene analysis. Within the finely mapped QTL intervals, candidate genes that are expressed in brain will be sequenced in the progenitor strains to look for functional polymorphisms. Expression level of the candidate genes in brain regions will be compared in the progenitor strains. 3. Initiation of mutagenesis studies of aggressive behaviors. ENU mutagenesis and gene-trap studies of aggressive behaviors in mice will be initiated. ENVIRONMENT: The training will be conducted at the Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania School of Medicine. RESEARCH CAREER DEVELOPMENT: The candidate will take relevant courses at Penn and elsewhere and will attend research meetings. Dr. Wade Berrettini will be the mentor, and Drs. Maja Bucan, Russell Buono, Thomas Ferraro, and Irwin Lucki will provide additional consultation in genetics and behavioral analysis.

描述（由申请人提供）：本提案旨在提供爱德华S。Brodkin，医学博士经过为期五年的监督研究培训，他将成为一名独立的研究人员，研究重点是小鼠攻击行为的遗传解剖。候选人将获得在数量性状基因座（QTL）的高分辨率遗传作图，候选基因分析和诱变方法方面的培训和经验。 背景：攻击行为是严重神经精神障碍患者发病率和死亡率的主要来源。哺乳动物的攻击倾向基本上是可以遗传的。小鼠攻击行为的遗传解剖可以识别哺乳动物攻击行为的生物学途径，并可能参与人类精神疾病的病理生理学。Brodkin博士先前已经在NZB/B1 NJ和A/J小鼠的10号染色体（Aggr 1）和X号染色体（Aggr 2）上鉴定了攻击性QTL;然而，他以前没有高分辨率（精细）QTL定位，候选基因分析或诱变方法的经验。这些方法的培训对候选人的职业发展很重要，也是他未来独立研究的必要条件。 研究计划的具体目标：1。精细定位攻击性QTL。使用NZB/B1 NJ和AJ小鼠作为祖先品系，将针对Aggr 1和Aggr 2 QTL间隔培育间隔特异性同源品系，并将其用于精细定位QTL间隔。2.候选基因分析。在精细定位的QTL区间内，将在祖先品系中对在脑中表达的候选基因进行测序以寻找功能多态性。将在祖细胞株中比较脑区域中候选基因的表达水平。3.攻击性行为的诱变研究的开始。将启动小鼠攻击行为的ENU诱变和基因陷阱研究。 环境：培训将在宾夕法尼亚大学医学院精神病学系神经生物学和行为中心进行。 研究职业发展：候选人将在宾夕法尼亚大学和其他地方参加相关课程，并将参加研究会议。Wade Berrettini博士将担任导师，Maja Bucan、Russell Buono、托马斯费拉罗和欧文卢基博士将提供遗传学和行为分析方面的额外咨询。