Genetic modulation of Wingless/Wnt signaling

Wingless/Wnt 信号传导的基因调节

• 批准号: 7753919
• 负责人: AMY M BEJSOVEC
• 金额: $ 28.57万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-01-01 至 2012-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7753919
• 关键词: Actins; Address; Adult; Affect; Animals; Antibodies; Binding; Biological Models; Cancer Etiology; Cell Nucleus; Cell division; Cell physiology; Cells; Chimeric Proteins; Colon Carcinoma; Colorectal Cancer; Complex; Cytokinesis; Cytoplasm; Cytoskeleton; DNA Binding; Development; Drosophila genus; Embryo; Embryonic Development; Epidermis; Felis catus; Funding; GTPase-Activating Proteins; Gene Expression; Gene Targeting; Genes; Genetic; Genetic Models; Genetic Transcription; Homologous Gene; Human; Immunoprecipitation; Invertebrates; Kidney; Kinesin; Knock-out; Laboratories; Life; Location; Malignant Neoplasms; Mechanics; Mediating; Modeling; Modification; Mutation; Names; Pathway interactions; Pattern; Play; Positioning Attribute; Process; Proteins; RNA Interference; Regulation; Regulator Genes; Reporter; Repression; Research; Role; Saints; Salsola; Signal Pathway; Signal Transduction; Specific qualifier value; System; Techniques; Tertiary Protein Structure; Testing; Tissues; Transcriptional Activation; Transgenes; Transgenic Organisms; Tumor Suppressor Proteins; Undifferentiated; Whole Organism; Work; Yeasts; activating transcription factor; cell transformation; chromatin immunoprecipitation; embryonic cell culture; fly; intestinal epithelium; loss of function; novel; programs; promoter; public health relevance; research study; response; stem cell population; yeast two hybrid system

DESCRIPTION (provided by applicant): Wnt signaling determines cell fates during embryonic development in all animals, including humans, and is required later in life to maintain stem cell populations. Excess Wnt activity is associated with human cancers, particularly colon cancer. To understand how Wnt signaling causes cancer, the factors that normally control Wnt pathway activity must be fully characterized. The long term objective of the Bejsovec laboratory is to dissect the mechanics of this important signaling pathway, using both the Drosophila genetic model system and cultured human cells. This lab has identified by mutational analysis many important pathway components, such as Tcf, the transcription factor that activates Wnt target genes, and Apc2, a human tumor suppressor homolog that negatively regulates the Wnt pathway. This proposal focuses on another negative regulatory gene identified in the same mutational screen: tumbleweed (tum) is a homolog of the human RacGap1, a GTPase activating protein (GAP). Surprisingly, the GAP activity of this gene is essential for cell division, but its GAP activity is not required for its role in Wnt regulation. Two Tum-interacting molecules, identified in yeast two- hybrid screens, strongly modulate Wnt pathway activity in human cells. Pavarotti (Pav), a kinesin-like protein, acts as a repressor in a similar fashion to Tum, while the other interactor, a novel fly protein tentatively named Sills, enhances Wnt-induced target gene expression. This application proposes three aims to determine the mechanism of action for Tum and its binding partners. Both Tum and Pav play a Wnt-independent role in organizing the cytoskeleton during cell division, so a primary issue is whether their Wnt- dependent role also occurs in the cytoplasm. Aim 1 will determine the subcellular locations relevant to their Wnt-modulating activity. Aim 2 will address whether Tum and Pav interact directly with other Wnt pathway components or with the transcription complex that forms on Wnt target gene promoters. Aim 3 will characterize the cellular function of Sills and its human homolog, using both fly embryos and cultured cells to determine how it enhances Wnt activity. These experiments will help formulate a clearer picture of how living tissue modulates the response to Wnt signal. PUBLIC HEALTH RELEVANCE: Wnt signaling is essential for normal development in all animals, but abnormal Wnt signaling is associated with various forms of cancer, particularly colorectal cancer. Experiments proposed here will use both the fruitfly model system and cultured human cells to study newly-discovered genetic factors that regulate Wnt signaling.

描述（由申请人提供）：Wnt信号传导决定了所有动物（包括人类）胚胎发育期间的细胞命运，并且在以后的生活中需要维持干细胞群。过量的Wnt活性与人类癌症，特别是结肠癌有关。为了了解Wnt信号是如何导致癌症的，必须充分表征通常控制Wnt通路活性的因素。Bejsovec实验室的长期目标是使用果蝇遗传模型系统和培养的人类细胞来剖析这一重要信号通路的机制。该实验室已经通过突变分析确定了许多重要的通路组分，例如Tcf，激活Wnt靶基因的转录因子，以及Apc2，一种负调节Wnt通路的人类肿瘤抑制因子同源物。该提案的重点是在同一突变筛选中鉴定的另一个负调控基因：风滚草（tumbleweed，tum）是人类RacGap1的同源物，RacGap1是一种GT3激活蛋白（GAP）。令人惊讶的是，该基因差距活性对于细胞分裂是必需的，但其GAP活性对于其在Wnt调控中的作用不是必需的。在酵母双杂交筛选中鉴定的两种Tum相互作用分子强烈调节人细胞中的Wnt途径活性。Pavarotti（Pav）是一种类似于Tum的驱动蛋白，以类似于Tum的方式作为阻遏物，而另一种相互作用物，一种暂时命名为Sills的新型苍蝇蛋白，增强了Wnt诱导的靶基因表达。本申请提出了三个目的来确定Tum及其结合伙伴的作用机制。Tum和Pav在细胞分裂期间在组织细胞骨架中均发挥Wnt非依赖性作用，因此主要问题是它们的Wnt依赖性作用是否也发生在细胞质中。目的1将确定与其Wnt调节活性相关的亚细胞位置。目的2将解决Tum和Pav是否直接与其他Wnt途径组分或与Wnt靶基因启动子上形成的转录复合物相互作用。目的3将描述Sills及其人类同系物的细胞功能，使用苍蝇胚胎和培养细胞来确定它如何增强Wnt活性。这些实验将有助于更清楚地了解活组织如何调节对Wnt信号的反应。公共卫生关系：Wnt信号传导对于所有动物的正常发育都是必不可少的，但异常的Wnt信号传导与各种形式的癌症，特别是结直肠癌有关。这里提出的实验将使用果蝇模型系统和培养的人类细胞来研究新发现的调节Wnt信号传导的遗传因子。