Recombineering based analysis of Hox function in kidney development

基于重组工程的肾脏发育中 Hox 功能分析

• 批准号: 8701721
• 负责人: S. Steven Potter
• 金额: $ 33.93万
• 依托单位: CINCINNATI CHILDRENS HOSP MED CTR
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-08-08 至 2018-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8701721
• 关键词: Binding Sites; Biological; Biological Process; Body part; Cell Proliferation; Cells; ChIP-seq; Complement; DNA; DNA Binding; Data; Databases; Development; Diagnosis; Dissection; Drosophila genus; Enhancers; Failure; Frameshift Mutation; Future; Gene Expression; Gene Expression Profile; Gene Mutation; Gene Targeting; Genes; Genetic; Head; Histology; Hydronephrosis; In Situ Hybridization; Kidney; Lead; Left; Leg; Link; Lower urinary tract; Mammals; Mediating; Mesenchyme; Metanephric Diverticulum; Microfluidics; Modeling; Molecular; Mus; Mutant Strains Mice; Mutate; Mutation; Natural regeneration; Nephrons; Ontology; Organism; Pathway interactions; Pattern; Phenotype; Process; Proteins; RNA; Regulation; Research; Resources; Role; Sorting - Cell Movement; Stem cells; Testing; Vesicle; Work; base; design; gene function; imaginal disc; improved; induced pluripotent stem cell; insight; interest; laser capture microdissection; mutant; nephrogenesis; novel; paralogous gene; public health relevance; transcription factor; transcriptome sequencing

DESCRIPTION (provided by applicant): The Hox genes are among the key genetic regulators of development. Mutations of these genes in simple organisms can cause dramatic transformations of body parts, with legs for example protruding from the head in place of antennae. In mammals, however, mutations generally give considerably milder effects. This is likely the result of the much greater number of Hox genes in mammals and their extensive overlapping functions. In this proposal we describe a novel recombineering strategy that allows us to simultaneously introduce frameshift mutations into sets of contiguous Hox genes, while leaving interspersed shared enhancers intact. We propose to complete the creation of a rich resource of Hox mutant mice that will allow the dissection of both flanking and paralogous Hox gene functional relationships. While 31 Hox genes show robust expression during kidney development, developmental functions have only been identified for six. We propose to unveil the roles of the other Hox genes by creating mice with stepwise reductions in Hox flanking and paralogous function. Preliminary studies of mice already made with mutations in HoxD, 3, 4, 8 and HoxA9, 10, 11, HoxC9, 10, 11 and HoxD9, 10, 11, have identified interesting phenotypes, including dramatic reductions in nephron number, glomerulomegaly, hydronephrosis, and failure to make renal vesicles, discovering the importance of additional Hox genes in kidney development. We also propose an extensive analysis of resulting kidney phenotypes, leveraging our GUDMAP consortium expertise and database. The moleular mechanisms of Hox function will be defined through characterization of overlapping sets of downstream targets and Gene Ontology analysis defining their molecular functions and biological processes. The study of disturbed kidney gene expression patterns in Hox mutants will extend to the single cell level, using novel microfluidics/RNA-Seq approaches. In addition Chip-Seq will be used to define the overlapping sets of Hox DNA binding sites and to distinguish direct targets. The results will improve our understanding of the genetic circuitry of kidney development and will thereby augment future DNA diagnosis and iPS mediated regeneration and/or replacement of diseased or malformed kidneys.

描述（由申请人提供）：Hox基因是发育的关键遗传调节因子之一。在简单的生物体中，这些基因的突变可以导致身体部位的巨大变化，例如腿从头部伸出，而不是触角。然而，在哺乳动物中，突变通常会产生相当温和的影响。这可能是由于哺乳动物中Hox基因的数量要多得多，而且它们的功能广泛重叠。在这个建议中，我们描述了一种新的重组策略，使我们能够同时引入移码突变成组的连续Hox基因，而留下散布的共享增强子完整。我们建议完成丰富的Hox突变小鼠资源的创建，这将允许剖析侧翼和旁系同源Hox基因的功能关系。 虽然有31个Hox基因在肾脏发育过程中表现出强大的表达，但只有6个基因的发育功能被确定。我们建议通过逐步减少Hox侧翼和旁系同源功能来揭示其他Hox基因的作用。对HoxD，3，4，8和HoxA，10，11，HoxC，9，10，11和HoxD，10，11突变的小鼠进行的初步研究已经确定了有趣的表型，包括肾单位数量急剧减少，肾小球肿大，肾积水和肾泡形成失败，发现了额外的Hox基因在肾脏发育中的重要性。我们还建议利用我们的GUDMAP联盟的专业知识和数据库，对由此产生的肾脏表型进行广泛的分析。Hox功能的分子机制将通过重叠的下游靶标集的表征和定义其分子功能和生物学过程的基因本体论分析来定义。Hox突变体中肾脏基因表达模式紊乱的研究将扩展到单细胞水平，使用新的微流体/RNA-Seq方法。此外，Chip-Seq将用于定义Hox DNA结合位点的重叠集并区分直接靶标。这些结果将提高我们对肾脏发育遗传电路的理解，从而增强未来的DNA诊断和iPS介导的再生和/或患病或畸形肾脏的替代。