Transcription Factor Networks in Cardiac Hypertrophy

心脏肥大中的转录因子网络

• 批准号: 7056336
• 负责人: Lina A Shehadeh
• 金额: $ 5.04万
• 依托单位: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-04-08 至 2009-04-07
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7056336
• 关键词: acyltransferase; animal data; biochemical evolution; cardiac myocytes; chromatin immunoprecipitation; computer program /software; deoxyribonuclease I; disease /disorder model; gene expression; genetic models; genetic promoter element; genetic regulation; heart enlargement; human data; laboratory mouse; laboratory rat; mathematical model; microarray technology; molecular biology information system; postdoctoral investigator; tissue /cell culture; transcription factor; ventricular hypertrophy

DESCRIPTION (provided by applicant): The broad objective is to develop an analysis strategy for heart expression data and use it to identify without any preconceived knowledge of disease-associated genes the key genes, their targets, and their regulatory pathway, and to validate these results in biological systems. Specific Aims are: I: Link hypertrophy associated genes to transcriptional regulatory networks. II: Optimize the strategy for application to other cardiac gene expression data sets. Health Relatedness: A better understanding of the function of a p300- driven network in vivo is essential to guiding drug development both in cancer and heart disease. The experimental design includes running microarrays on murine models of hypertrophy, generating and applying novel statistical approaches to microarray data to extract genes related to hypertrophy, generating mathematical representations to visualize global expression profiles in 3D, studying promoter organization in silico to identify complex regulatory elements, searching the eukaryotic promoter database for these complex elements to find co-regulated genes, validating the complex elements in vivo using ChIP assay, overlapping the network from microarrays and literature to promoter driven network to find unknown candidate genes.

描述(由申请人提供)：广泛的目标是开发心脏表达数据的分析策略，并使用它在没有任何疾病相关基因先入为主的知识的情况下识别关键基因、它们的靶点和它们的调控途径，并在生物系统中验证这些结果。具体目标是：i：将肥大相关基因与转录调控网络联系起来。II：优化策略以应用于其他心脏基因表达数据集。与健康相关：更好地了解体内p300驱动的网络的功能对于指导癌症和心脏病的药物开发至关重要。实验设计包括在小鼠肥大模型上运行微阵列，产生并应用新的统计方法来提取与肥大相关的基因，产生数学表示以三维可视化全球表达谱，研究电子计算机中的启动子组织以识别复杂的调控元件，在真核启动子数据库中搜索这些复杂元件以寻找共同调控的基因，使用芯片分析验证体内的复杂元件，重叠从微阵列和文献到启动子驱动网络的网络以寻找未知的候选基因。