Factors Involved in Transcription by RNA Polymerase II

RNA 聚合酶 II 转录涉及的因素

• 批准号: 8116396
• 负责人: David H Price
• 金额: $ 6万
• 依托单位: UNIVERSITY OF IOWA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-08-13 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8116396
• 关键词: Address; Animal Model; Binding; Biochemical; Biological Assay; Cell Nucleus; Cells; Chromatin Structure; Cisplatin; Coupled; Cyclin-Dependent Kinases; DNA Damage; DNA Repair; Defect; Development; Double-Stranded RNA; Drosophila genome; Drosophila genus; Environment; Fluorescence Recovery After Photobleaching; Genes; Genetic Transcription; Genome; Goals; Human; In Vitro; Interphase Cell; Iowa; Location; Malignant Neoplasms; Maps; Mediating; Medicine; Messenger RNA; Methods; MicroRNAs; Mitosis; Mitotic; Molecular; Mus; Nuclear Export; Organism; Pathology; Phosphorylation; Play; Polymerase; Positive Transcriptional Elongation Factor B; Process; Production; Proteins; RNA Binding; RNA Polymerase II; Regulation; Repression; Research; Research Personnel; Role; Signal Transduction; Site; Small Nuclear Ribonucleoproteins; System; Technology; Time; Transcription Elongation; Transcription-Coupled Repair; Universities; Work; abstracting; chromatin immunoprecipitation; college; factor EF-P; fly; genome-wide; improved; in vivo; insight; knock-down; negative elongation factor; novel; premature; professor; promoter; public health relevance; reconstitution; repaired; research study; termination factor

DESCRIPTION (provided by applicant): ABSTRACT It has become apparent that RNA polymerase II (RNAPII) elongation control plays a major role in regulating transcription throughout development and differentiation of multi-cellular organisms. The process is characterized by the default action of negative elongation factors, including NELF and DSIF that halt transcription of initiated polymerases near promoters. These poised polymerases are either released from the template by TTF2 or other termination factors or are allowed to enter productive elongation through the selective action of the positive elongation factor, P-TEFb. The cyclin dependent kinase activity of P-TEFb is regulated by reversible association with the 7SK snRNP mediated by HEXIM proteins. The main goal of this proposal is to further define the mechanisms utilized to control RNAPII elongation. The approach will employ biochemical and molecular methods in human and mouse cells and in the model organism, Drosophila. In the first aim, the function of P-TEFb and the potential role of premature termination in regulating transcription will be studied. Part of the plan includes in vitro biochemical approaches; however global analyses are planned in which transcription of all genes will be examined using chromatin immunoprecipitation followed by massively parallel sequencing (ChIP-seq). The second aim focuses on cellular mechanisms utilized to control P- TEFb and how these may involved in conferring selectivity to the genes activated by P-TEFb. Here again genome wide mapping of P-TEFb regulatory factors will be carried out. In the final aim the roles of the termination factor TTF2 will be addressed. In addition to its role in mitotic repression of transcription elongation, studies will examine its role in transcription coupled DNA repair, premature termination at the 52 end of genes, and in termination following normal 32 end formation. The principle investigator is a professor at the University of Iowa and this project will be carried out in the excellent environment offered by his lab and the facilities in the University of Iowa, College of Medicine. PUBLIC HEALTH RELEVANCE: Project Narrative The proposed research in this application will make a major contribution toward understanding the basic cellular mechanisms that control transcription. It is critical to understand how transcription is regulated because abnormalities in this process are responsible developmental defects, cancer and other pathologies.

描述（由申请人提供）：