Mechanisms and Function of Myonuclear Positioning

肌核定位的机制和功能

• 批准号: 8915054
• 负责人: MARY K BAYLIES
• 金额: $ 40.31万
• 依托单位: SLOAN-KETTERING INST CAN RESEARCH
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-01 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8915054
• 关键词: Address; Affect; Architecture; Area; Biochemical; Biological; Biological Assay; Biological Markers; Biological Models; Biology; Cell Nucleus; Cell physiology; Cells; Centronuclear myopathy; Communication; Cytoskeleton; Data; Defect; Development; Disease; Drosophila genus; Dynein ATPase; Etiology; Gene Expression Profile; Genes; Genetic; Genetic Screening; Genomic approach; Goals; Growth; Growth and Development function; Health; Homeostasis; Human; Image; Investigation; Kinesin; Knowledge; Lead; Light; Link; MAPK8 gene; Methodology; Microtubule-Associated Proteins; Microtubules; Minus End of the Microtubule; Mitochondria; Motor; Motor Neurons; Movement; Mus; Muscle; Muscle Cells; Muscle Development; Muscle Fibers; Muscle function; Mutation; Myopathy; Myotonic Dystrophy; Nature; Neuromuscular Junction; Neurons; Normal Cell; Nuclear; Nuclear Envelope; Organelles; Output; Physiological; Physiology; Plus End of the Microtubule; Positioning Attribute; Process; Processed Genes; Protein Isoforms; Proteins; Publishing; Regulation; Research; Role; Sarcomeres; Shapes; Signal Transduction; Striated Muscles; System; Tendon structure; Testing; Time; Work; cell type; gene conservation; genetic analysis; genetic approach; genetic resource; human disease; in vivo; insight; muscle strength; mutant; neuromuscular; neuromuscular activity; ninein; novel; novel strategies; regenerative; relating to nervous system; research study; sensor; therapeutic target; time use; transcriptome sequencing

DESCRIPTION (provided by applicant): Our long-term goal is to significantly impact the knowledge of muscle biology and provide new approaches for disease treatment. Striated muscle fibers are large multinucleated cells and possess a highly organized cytoarchitecture containing organelles positioned for optimal muscle function. This positioning is particularly evident in the placement of myonuclei, which reside above the sarcomere at the periphery of the myofiber and are positioned to maximize their internuclear distance. Our objective is the identification of mechanisms responsible for myonuclear movement and positioning. Centrally located myonuclei have been used for decades as a hallmark of muscle disease. However, little is known about the mechanisms that control myonuclear movement normally, or the contribution of aberrant myonuclear position to the etiology and/or progression of muscle disease. Building on our recently published results (Metzger et al., Nature, 2012; Folker et al., Development, 2012), our specific aims in this proposal are to characterize new genes involved in myonuclear positioning, address how tendon and motorneurons fine-tune myonuclear positioning during muscle function, and investigate why muscles fail to function optimally when myonuclei are mispositioned. This proposal will identify physiological changes that result from aberrant nuclear placement, providing new biomarkers/therapeutic targets to examine/treat muscle disease. Lastly, these data will shed light on how the organization of the muscle fiber cytoarchitecture is achieved during development and growth. Our investigation will be primarily carried out in Drosophila; however, we will test our paradigm in mammalian muscle cultures. Our methodologies take advantage of cutting edge, in vivo time lapse imaging that we have developed in Drosophila to follow myonuclear movement and cytoskeletal dynamics. We will employ the genetic resources available in Drosophila to manipulate genes, processes, and cell types for our analyses. These genetic experiments will be supported by biochemical and cell biological approaches. Muscle physiology will be investigated by assaying mitochondrial output via quantification of ATP and ROS levels, including using a novel ROS sensor for the latter, and neuromuscular communication, and importantly muscle cellular output, via electrophysiological approaches. Genomic approaches, specifically RNAseq, will reveal changes in the muscle transcriptome as a result of improper myonuclear position. Together the work outlined in this proposal will shed new light on this little understood but important area of muscle biology. The results of this research will permit us to highlight genes and mechanisms that are candidates for changes associated with different human muscle diseases.

描述（由申请人提供）：我们的长期目标是显著影响肌肉生物学知识，并为疾病治疗提供新方法。横纹肌纤维是大的多核细胞，具有高度组织化的细胞结构，包含定位于最佳肌肉功能的细胞器。这种定位在肌核的放置中特别明显，肌核位于肌纤维周围的肌节上方，并定位成使其核间距离最大化。我们的目标是识别负责肌运动和定位的机制。数十年来，位于中央的肌核一直被用作肌肉疾病的标志。然而，很少有人知道的机制，控制正常的肌肉运动，或异常的肌肉位置的病因和/或肌肉疾病的进展的贡献。基于我们最近发表的结果（Metzger等人，Nature，2012; Folker等人，Development，2012），我们在该提案中的具体目标是表征参与肌细胞定位的新基因，解决肌腱和运动神经元如何在肌肉功能期间微调肌细胞定位，并研究为什么当肌核错位时肌肉无法发挥最佳功能。该提案将识别由异常核放置引起的生理变化，提供新的生物标志物/治疗靶点来检查/治疗肌肉疾病。最后，这些数据将揭示肌纤维细胞结构的组织是如何在发育和生长过程中实现的。我们的研究将主要在果蝇中进行;然而，我们将在哺乳动物肌肉培养物中测试我们的范例。我们的方法利用尖端的，在体内的时间推移成像，我们已经在果蝇中开发，以遵循myocellular运动和细胞骨架动力学。我们将利用果蝇的遗传资源来操纵基因、过程和细胞类型，以进行分析。这些遗传实验将得到生物化学和细胞生物学方法的支持。肌肉生理学将通过ATP和ROS水平的定量测定线粒体输出来研究，包括使用新型ROS传感器用于后者，以及神经肌肉通讯，重要的是肌肉细胞输出，通过电生理学方法。基因组方法，特别是RNAseq，将揭示肌肉转录组的变化，由于不适当的肌层位置。这项提案中概述的工作将为肌肉生物学这一鲜为人知但重要的领域提供新的见解。这项研究的结果将使我们能够突出与不同人类肌肉疾病相关的变化的候选基因和机制。