The Role of microRNA in Pancreas Development

microRNA 在胰腺发育中的作用

• 批准号: 7586811
• 负责人: Michael S German
• 金额: $ 31.04万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7586811
• 关键词: Affect; Alleles; Applications Grants; Beta Cell; Cell Differentiation process; Cells; Chromatin; Data; Defect; Development; Diabetes Mellitus; Embryo; Endoribonucleases; Functional RNA; Gene Expression; Gene Expression Regulation; Gene Targeting; Generations; Genes; German population; Glucose; Goals; In Situ Hybridization; In Vitro; Individual; Insulin; Islet Cell; Islets of Langerhans; Medical; Messenger RNA; Methods; MicroRNAs; Mus; Oligonucleotide Microarrays; Pancreas; Pathway interactions; Patients; Pattern; Process; Production; Regulation; Research Personnel; Role; Site; Testing; Tissues; Transgenic Organisms; base; cell type; direct application; endocrine pancreas development; endoribonuclease; homeodomain; human DICER1 protein; insulin secretion; interest; islet; pancreas development; precursor cell; programs; promoter; recombinase; research study; transcription factor

DESCRIPTION (provided by applicant): The goal of this proposal is to determine the role of small non-coding microRNAs (miRNA) in pancreatic islet development. We hypothesize that miRNA regulate the expression of genes controlling islet development. Although miRNA are known to influence the development of several tissues, and they have been implicated in glucose-stimulated insulin secretion in mature beta-cells, the role of miRNA in pancreatic development has not been explored previously. The specific aims of this proposal are to establish the global role of miRNA in pancreas and islet development and to understand the role of individual miRNA: 1. Test the importance of miRNA in pancreas development by removing either Dicer or DGCR8, two components of the pathway for processing miRNA, from early pancreatic precursor cells with pdx1-cre, early islet precursor cells with ngn3-cre, and mature beta-cells with ins2-cre. 2. Determine the expression pattern of miRNAs during pancreas development. We will use miRNA oligonucleotide microarrays that we have already developed and tested, in situ hybridization, and BAG transgenics to determine the expression pattern of miRNAs during pancreatic development. 3. Test the role of specific miRNA in regulating expression of pancreatic transcription factors. Based on predicted miRNA targets, we will focus on the regulation of homeodomain factor Nkx6.1. 4. Establish the mechanisms for regulation of miRNA expression in the pancreas. We will test specifically for regulation of miRNA by pancreatic transcription factors Sox9, Neurogenin3 and Nkx2.2. These studies will help us understand how islet cells differentiate and the role of miRNA in that process. A better understanding of how islet cells differentiate will help in developing methods for producing islet cells for patients with diabetes.

描述（由申请人提供）：该提案的目的是确定小型非编码microRNA（miRNA）在胰岛发育中的作用。我们假设miRNA调节控制胰岛发育的基因的表达。尽管已知miRNA会影响多种组织的发育，并且它们与成熟β细胞中葡萄糖刺激的胰岛素分泌有关，但MiRNA在胰腺发育中的作用尚未探索。该提案的具体目的是确定miRNA在胰腺和胰岛发展中的全球作用，并了解单个miRNA的作用：1。通过去除dicer或dgcr8来测试miRNA在胰腺发育中的重要性，这是培养途径的两个组成部分，该途径与早期的pancreatic cells cell in MiRNA的两个组成部分与PDX1-CRER 3的早期细胞和早期的MiRNA一起处理，并将其与早期的MiRNA进行处理。带有INS2-CRE的β细胞。 2。确定胰腺发育过程中miRNA的表达模式。我们将使用我们已经开发和测试的MiRNA寡核苷酸微阵列，并在原位杂交和袋子转基因中确定胰腺发育过程中miRNA的表达模式。 3。测试特定miRNA在调节胰腺转录因子表达中的作用。基于预测的miRNA靶标，我们将重点关注同源域因子NKX6.1的调节。 4。建立调节胰腺中miRNA表达的机制。我们将通过胰腺转录因子SOX9，Neurogenin3和NKX2.2专门测试miRNA。这些研究将有助于我们了解胰岛细胞如何区分和miRNA在该过程中的作用。更好地了解胰岛细胞如何区分将有助于开发用于糖尿病患者的胰岛细胞的方法。