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Regeneration and transdetermination of imaginal discs of Drosophila

果蝇成虫盘的再生和转决定

基本信息

批准号：
7769490
负责人：
H.D. Toby BRADSHAW
金额：
$ 30.89万
依托单位：
UNIVERSITY OF WASHINGTON
依托单位国家：
美国
项目类别：
财政年份：
1998
资助国家：
美国
起止时间：
1998-05-01 至 2013-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7769490
关键词：
Address Adult Affect Animals Area Binding Sites Biological Assay Biological Models Candidate Disease Gene Cell Lineage Cell division Cells Clone Cells DNA Binding DNA Microarray Chip Data Development Dose Drosophila genus Embryonic Development Enhancers Ensure Environment Event Exhibits Frequencies Generations Genes Genetic Genetic Enhancer Element Goals Homeostasis Injury Interstitial Collagenase Larva Lectin Life Link Liver Regeneration Maintenance Mediating Microarray Analysis Modification Molecular Molecular Profiling Moon Mus Mutation Natural regeneration Normal tissue morphology Orthologous Gene Pathway interactions Pattern Phenotype Property Proteins Reproduction Role Signal Pathway Signal Transduction Spottings Stem cells Testing Time Tissues Twin Multiple Birth Work Zebrafish cell behavior chromatin remodeling computerized data processing daughter cell developmental plasticity human disease imaginal disc insight multipotent cell mutant novel overexpression repaired research study stem cell biology stem cell division transdetermination

项目摘要

DESCRIPTION (provided by applicant): Drosophila imaginal discs are able to regenerate and thus provide us with a model system to study multipotency of cells. Under certain conditions a small set of cells in the "weak point" of each imaginal disc change their fate. This switch, known as transdetermination (TD), occurs with high frequency when wg is overexpressed or when a disc is cut through the "weak point". Expression profiling of these cells identified candidate genes which in functional tests significantly modified TD. Some of these candidates are chromatin-remodeling genes. Furthermore, we identified putative regeneration genes such as alr-like, a gene orthologous to the mouse gene augmenter of liver regeneration (alr), Matrix metalloproteinase 1 (Mmp1), and dReg, a novel gene that contains a C-lectin domain. Although the mammalian orthologs of these three genes have been linked to regeneration of specific tissues, the mechanism by which they act is not well understood. We propose to continue and complete the functional tests, including the generation of mutations in novel candidate Drosophila genes. Dr. Moon will test homologous zebrafish genes. In examining regeneration, the issue of stem cells must be addressed. Do TD cells divide like stem cells? Cell clones will be induced in TD cells to assay for asymmetrical divisions, a landmark of stem cell behavior. These analyses will then be performed in the presence and absence of characterized enhancers and suppressors of TD to test whether these genes affect developmental plasticity by modifying the cell lineage pattern, the number of founder cells or the cell-doubling times. This proposal will contribute to the understanding of which molecular signals increase regeneration potential to ensure normal tissue maintenance and repair. Short summary A few specific cells in each imaginal disc of Drosophila have stem cell properties. If challenged by injury they regenerate. We will test whether these cells divide asymmetrically, a landmark of stem-cell behavior. In addition, we will identify the genes that mediate developmental plasticity and test how their gene products affect multipotent cells and their surroundings. Drosophila has been used as a model system to study human disease and we see here an opportunity to gain insight into stem-cell biology and regeneration.

描述（由申请人提供）：果蝇成虫盘能够再生，因此为我们提供了研究细胞多能性的模型系统。在某些条件下，在每个成虫盘的“弱点”中的一小部分细胞改变了它们的命运。这种开关，称为transdetermination（TD），当wg过度表达或当椎间盘被切割通过“弱点”时，会以高频率发生。这些细胞的表达谱鉴定了在功能测试中显著修饰TD的候选基因。这些候选基因中的一些是染色质重塑基因。此外，我们确定了假定的再生基因，如alr样，基因正交的小鼠肝再生基因增强因子（alr），基质金属蛋白酶1（Mmp 1），和dReg，一个新的基因，包含一个C-凝集素结构域。虽然这三个基因的哺乳动物直系同源物与特定组织的再生有关，但它们的作用机制还不清楚。我们建议继续并完成功能测试，包括在新的候选果蝇基因中产生突变。穆恩博士将测试同源的斑马鱼基因。在研究再生时，必须解决干细胞的问题。TD细胞像干细胞一样分裂吗？将在TD细胞中诱导细胞克隆以测定不对称分裂，这是干细胞行为的标志。然后在存在和不存在TD的特征性增强子和抑制子的情况下进行这些分析，以测试这些基因是否通过改变细胞谱系模式、创始细胞数量或细胞倍增时间来影响发育可塑性。该建议将有助于了解哪些分子信号增加再生潜力，以确保正常的组织维护和修复。在果蝇的每个成虫盘中有一些特定的细胞具有干细胞特性。如果受到伤害，它们会再生。我们将测试这些细胞是否不对称分裂，这是干细胞行为的标志。此外，我们将确定介导发育可塑性的基因，并测试它们的基因产物如何影响多能细胞及其周围环境。果蝇一直被用作研究人类疾病的模型系统，我们在这里看到了一个深入了解干细胞生物学和再生的机会。