Mechanisms of Steroid-Triggered Programmed Cell Death

类固醇触发的程序性细胞死亡的机制

• 批准号: 7274140
• 负责人: CARL S. THUMMEL
• 金额: $ 35.44万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-04-01 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7274140
• 关键词: Affect; Alleles; Animals; Apoptosis; Biological; Biological Metamorphosis; Biological Models; Cell Death; Cells; Cessation of life; Chromosomes; Defect; Depth; Development; Disease; Down-Regulation; Drosophila genus; Drosophila inhibitor of apoptosis 1; EP300 gene; Ecdysone; Event; Foundations; Genes; Genetic; Genetic Screening; Genetic Transcription; Genome; Goals; Green Fluorescent Proteins; Hormonal; Hormones; Human; Lead; Life; Link; Maps; Molecular; Mutagenesis; Mutation; Nuclear Receptors; Organism; Orthologous Gene; Pathway interactions; Personal Satisfaction; Phenotype; Physiological; Play; Range; Regulation; Research Personnel; Role; Salivary Glands; Signal Transduction; Sorting - Cell Movement; Staging; Steroids; TATA Box Binding Protein-Like Proteins; Testing; Tissues; Work; base; gene function; human disease; mutant; novel; programs; response; steroid hormone; tool; transcription factor

Small lipophilic hormones, acting through their corresponding nuclear receptors, control a wide range of developmental and physiological responses in higher organisms. Although extensive studies have focused on the mechanisms by which nuclear receptors control target gene transcription, relatively little is known about how a hormonal signal is transduced into an appropriate biological response during development. We propose to define one such pathway in detail - steroid-triggered cell death - using Drosophila as a model system. It is well known that steroids play a central role in controlling cell death in higher organisms, including humans. Only in Drosophila, however, has a genetic cascade been identified that links the hormone to a death response - the destruction of the larval salivary glands in response to the steroid hormone ecdysone during metamorphosis. We propose to build off this foundation, using an open-ended genetic screen to identify key players in this pathway. By using GFP as a marker for salivary glands in living animals, we will identify mutants that show specific defects in the steroid-triggered death response. A pilot screen has demonstrated the feasibility of this approach. We identified known genes in the death pathway as well as several new players, including genes that encode the CBP transcriptional co-factor and the TBP-related factor, TRF2. We propose to characterize these two genes in detail, defining the mechanisms that link them to cell death. We also propose to expand our search for death regulators through saturation mutagenesis of approximately 40% of the genome. Mutations will be mapped to specific genes, and functions for these genes will be assigned. This work provides a basis for understanding the molecular mechanisms of hormone signal transduction - defining the players in a genetic cascade that link the hormone to a stage- and tissue-specific biological response during development. This work also represents the first attempt to use random mutagenesis to dissect an endogenous programmed cell death response in Drosophila, raising the possibility that we will uncover novel death regulators. Finally, our studies provide a foundation for determining how steroids control cell death in humans, with implications for understanding and treating human disease.

在高等生物中，小的亲脂激素通过其相应的核受体起作用，控制着广泛的发育和生理反应。尽管大量的研究集中在核受体控制靶基因转录的机制上，但对于激素信号在发育过程中如何被转导成适当的生物反应，人们知之甚少。我们建议用果蝇作为模型系统来详细定义一个这样的途径——类固醇引发的细胞死亡。众所周知，类固醇在控制包括人类在内的高等生物的细胞死亡中起着核心作用。然而，只有在果蝇身上，才发现了与这种激素有关的遗传级联反应