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The role of tomosyn-2 in insulin secretion

Tomosyn-2在胰岛素分泌中的作用

基本信息

批准号：
8766798
负责人：
Sushant Bhatnagar
金额：
$ 9万
依托单位：
UNIVERSITY OF WISCONSIN-MADISON
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-09-01 至 2016-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8766798
关键词：
Affect Animal Model Animals Area Award Binding Binding Proteins Biochemical Biochemistry Biological Assay Blood Glucose Breeding Cell Line Cell membrane Cell physiology Cells Chromosomes, Human, Pair 16 Code Complex Confocal Microscopy Congenic Mice Congenic Strain Cytoplasmic Granules Defect Development Disease Drug Targeting Epidemic Exocytosis Fasting Gelsolin Generations Genes Genetic Glucose Goals Grant Homeostasis Hyperglycemia Hypoglycemia In Vitro Insulin Insulin Resistance Intervention Knockout Mice Laboratories Learning Life Liposomes Maps Mass Spectrum Analysis Membrane Mentors Mouse Strains Mus Mutation Non-Insulin-Dependent Diabetes Mellitus Obesity Open Reading Frames Pancreas Pathway interactions Patients Peripheral Phase Phenotype Phosphorylation Phosphorylation Site Plasma Play Post-Translational Protein Processing Predisposition Proteins Quantitative Trait Loci Regulation Research Risk Role SNAP receptor Signal Pathway Signal Transduction Single Nucleotide Polymorphism Societies Techniques Therapeutic Training Ubiquitination Work career career development design diabetic experience fasting plasma glucose forward genetics genetic regulatory protein granule cell insight insulin granule insulin secretion islet member mouse model non-genetic novel pancreatic cell line peripheral blood prevent protein degradation public health relevance receptor risk variant secretion process synaptotagmin I syntaxin tool ubiquitin-protein ligase

项目摘要

DESCRIPTION (provided by applicant): Type 2 diabetes (T2D) is reaching epidemic proportions in Western societies. T2D occurs when the ¿-cells of the pancreas do not secrete enough insulin to properly regulate peripheral blood glucose levels, usually in the face of obesity and associated peripheral insulin resistance. The mechanisms underlying insulin secretion are not properly understood. Using a forward genetics approach, we have discovered that a single nucleotide polymorphism (SNP) in the protein-coding region of the gene for tomosyn-2 is directly correlated with the hypoinsulinemic/hyperglycemic phenotype. Tomosyn-2 is a relatively uncharacterized protein and the mechanism by which it regulates insulin secretion is not known. The work proposed here in this Pathways to Independence Award application has two primary goals: 1) to elucidate the mechanism by which tomosyn-2 regulates insulin secretion in pancreatic ¿-cells, and 2) to use my development of this novel area of T2D research to facilitate the development of my career from the mentored phase to an independent phase. During the mentored phase of the grant, I will receive training in mass spectrometry, in vitro liposome fusion assays, membrane biochemistry, and the generation of the tomosyn-2 knockout mouse. The research conducted in the mentored phase will examine the effect of identified phosphorylation sites on the ability of tomosyn-2 to regulate insulin secretion and to understand the mechanism by which tomosyn-2 is targeted for proteosomal degradation. During the independent phase of the grant, my research will examine the mechanism by which tomosyn-2 inhibits insulin secretion by regulating the activity of soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins and characterize the role of novel tomosyn-2 binding proteins. These studies will provide novel clues to the mechanism by which tomosyn-2 inhibits insulin secretion and will further our understanding of the regulation of insulin secretio in T2D.

描述（由申请人提供）：2型糖尿病（T2 D）在西方社会已达到流行比例。T2 D发生时，- 胰腺的细胞不能分泌足够的胰岛素来适当调节外周血糖水平，通常是在肥胖的情况下。以及相关的外周胰岛素抵抗。胰岛素分泌的机制还没有被正确理解。使用正向遗传学方法，我们已经发现tomosyn-2基因的蛋白质编码区中的单核苷酸多态性（SNP）与低胰岛素血症/高血糖表型直接相关。Tomosyn-2是一种相对不具有特征的蛋白质，其调节胰岛素分泌的机制尚不清楚。在独立之路奖申请中提出的工作有两个主要目标：1）阐明tomosyn-2调节胰腺细胞胰岛素分泌的机制，2）利用我对T2 D研究这一新领域的发展，促进我的职业生涯从指导阶段发展到独立阶段。在资助的指导阶段，我将接受质谱、体外脂质体融合试验、膜生物化学和tomosyn-2基因敲除小鼠的产生方面的培训。在指导阶段进行的研究将检查鉴定的磷酸化位点对tomosyn-2调节胰岛素分泌能力的影响，并了解tomosyn-2靶向蛋白体降解的机制。在资助的独立阶段，我的研究将研究tomosyn-2通过调节可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体（SNARE）蛋白的活性来抑制胰岛素分泌的机制，并表征新型tomosyn-2结合蛋白的作用。这些研究将为tomosyn-2抑制胰岛素分泌的机制提供新的线索，并将进一步加深我们对T2 D胰岛素分泌调节的理解。