Visualization of gene activity in the Drosophila embryo

果蝇胚胎中基因活性的可视化

• 批准号: 9981755
• 负责人: Michael Steven Levine
• 金额: $ 63.19万
• 依托单位: PRINCETON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-09-23 至 2021-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9981755
• 关键词: Affinity; Alleles; Animals; Biological Assay; Biological Sciences; Communication; Complex; DNA sequencing; Development; Disease; Dorsal; Drosophila genus; Embryo; Embryonic Development; Enhancers; Ensure; Funding; Gene Expression; Gene Expression Regulation; Genes; Genetic; Genetic Transcription; Genome; Goals; Grant; HOX protein; Human; Human Genome; Imaging technology; Memory; Methods; Methylation; Modeling; NF-kappa B; Population Heterogeneity; Process; Research; Resolution; System; Target Populations; Transgenes; Visualization; Work; follow-up; genomic locus; histone modification; imaging modality; insight; new technology; novel; programs; promoter; protein function; public health relevance; transcription factor

 DESCRIPTION (provided by applicant): During the past 25-30 years the two grants under consideration for merger in the MIRA program (GM46638 and GM34431) have provided numerous insights into the mechanisms underlying the control of gene expression during animal development. Specific highlights include evidence that Hox proteins function as sequence-specific transcription factors, the characterization of the complex eve stripe 2 enhancer, and the elucidation of the affinity threshold model for the differential regulation of gene expression by te Dorsal (NF-kB) gradient. These studies have established the early Drosophila embryo as a premiere system for the study of gene activity in animal development. It is the goal of the proposed MIRA grant to exploit the advent of new imaging technologies to uncover novel mechanisms of gene control. During the past year we have begun to use live imaging methods to visualize the dynamic regulation of gene expression during Drosophila embryogenesis. These studies have led to a number of striking observations that we wish to follow-up during the upcoming funding period, including transcriptional bursts of eve stripe 2 expressions, the non-additive activities of shadow enhancers, transcriptional memory, and allelic communication. We will determine whether transcriptional bursting is due to unstable enhancer-promoter looping interactions, and examine the possibility that the two alleles at a given genetic locus somehow communicate to ensure "balanced" levels of expression during development. The research plan includes four specific aims: 1) investigate the dynamics by which a single enhancer activates two different target promoters; 2) explore the possibility that temporal precision depends on "enhancer switching", whereby enhancers with overlapping activities work in a sequential manner during development; 3) determine whether transcriptional memory depends on specific histone modifications such as methylation; and 4) substantiate our preliminary evidence for allele communication by examining a variety of "sensitized" transgenes in living embryos.

 描述(由申请人提供)：在过去的25-30年里，MIRA计划中考虑合并的两笔赠款(GM46638和GM34431)为动物发育过程中基因表达控制的潜在机制提供了许多见解。具体的亮点包括HOX蛋白作为序列特异性转录因子发挥作用的证据，复杂的EVESTRIPE 2增强子的特征，以及通过TE背部(NF-kB)梯度对基因表达的差异调控的亲和力阈值模型的阐明。这些研究已经建立了果蝇早期胚胎作为研究动物发育中基因活性的首要系统。米拉基金的目标是利用新的成像技术的出现来揭示基因控制的新机制。在过去的一年里，我们已经开始使用实时成像方法来可视化果蝇胚胎发育过程中基因表达的动态调节。这些研究已经导致了一些引人注目的观察结果，我们希望在即将到来的资助期间进行后续研究，包括EVE条纹2表达的转录突发、阴影增强剂的非加性活动、转录记忆和等位基因交流。我们将确定转录爆发是否由于不稳定的增强子-启动子环相互作用，并检查给定遗传位点的两个等位基因以某种方式通信的可能性，以确保在发育过程中“平衡”的表达水平。该研究计划包括四个具体目标：1)研究单个增强子激活两个不同靶启动子的动力学；2)探索时间精确度取决于“增强子切换”的可能性，即具有重叠活性的增强子在发育过程中以顺序方式工作；3)确定转录记忆是否依赖于特定的组蛋白修饰，如甲基化；以及4)通过检测活胚胎中的各种“敏化”转基因，证实我们关于等位基因交流的初步证据。