Transgenic rat overexpressing miR-15/16 cluster:functional implications in develo

过表达 miR-15/16 簇的转基因大鼠：发育中的功能意义

• 批准号: 7929580
• 负责人: Junming Yue
• 金额: $ 7.4万
• 依托单位: UNIVERSITY OF TENNESSEE HEALTH SCI CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-10 至 2012-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7929580
• 关键词: Address; Adult; Biological; Biological Process; Cardiovascular Diseases; Development; Doxycycline; Embryo; Embryonic Development; Fibroblasts; Functional RNA; Gene Expression; Generations; Genes; Genotype; Growth; Human; Human Ubiquitin; Laboratories; Lead; Lentivirus Vector; Link; Malignant Neoplasms; Mediating; Messenger RNA; Metabolism; Methods; MicroRNAs; Microinjections; Modeling; Molecular; Molecular Profiling; Neurodegenerative Disorders; Nodal; Phenotype; Physiological; Proteins; Rattus; Reporter Genes; Research Personnel; Role; Rosa; Signal Pathway; Small RNA; Staging; Testing; Tetanus Helper Peptide; Tetracyclines; Tissues; Trans-Activators; Transgenic Organisms; Translations; Ubiquitin C; cdc Genes; gene function; human CCNE1 protein; human disease; insight; mouse model; overexpression; postnatal; promoter; receptor

DESCRIPTION (Provided by Applicant): MicroRNAs are a new class of non-coding small RNAs that negatively regulate gene expression by either degrading mRNA or suppressing protein translation. A miRNA cluster, miR-15/16, has been implicated in a variety of human diseases, such as cancer, and embryonic development. In particular, miR-15/16 was found to target the receptor Acvr2a, a core component of the Nodal signaling pathway, which is well-known to control embryogenesis. To gain more insight into this cluster's role in development and human diseases, the investigator proposes to generate two transgenic rat models: one is a ubiquitous transgenic rat (UBC-miR-15/16) that expresses miR-15/16 in all tissues using a human ubiquitin C promoter (UBC) in a lentiviral vector; Second is a tetracycline(Tet) inducible transgenic rat (Tet-miR-15/16), in which miR-15/16 cluster will be driven by Tet regulated lentiviral vector. The Tet-miR-15/16 transgenic rat will be crossed with a transgenic rat, Rosa26-rtTA-M2, that the reverse transactivator rtTA-M2 was driven by a ubiquitous promoter Rosa 26 the investigator generated in his laboratory recently to obtain a conditional double transgenic rat that expresses both the miR-15/16 and rtTA-M2. The expression of miR-15/16 cluster in this double transgenic rat will be tightly controlled by the doxycycline. This double transgenic rat model will provide an alternative approach to study the biological functions of miR-15/16 if the UBC-miR-15/16 transgenic rat model displays an embryonic lethal phenotype. The investigator will characterize these transgenic rats by genotyping, phenotyping of embryos, postnatals, and adults at different developmental stages using molecular biological, histological, and immunohistochemical approaches. Those two models will be highly valuable to address the molecular mechanisms by how miR-15/16 cluster is involved in multiple signaling pathways in development and other human diseases. PROJECT NARRATIVE: The ubiquitous and tetracycline inducible transgenic rats expressing miR-15/16 cluster will be generated to investigate their roles in development and other human diseases.

描述（由申请人提供）：MicroRNA是一类新的非编码小RNA，其通过降解mRNA或抑制蛋白质翻译来负调节基因表达。 一个miRNA簇，miR-15/16，已经涉及多种人类疾病，如癌症和胚胎发育。 特别是，发现miR-15/16靶向受体Acvr 2a，其是Nodal信号通路的核心组分，众所周知其控制胚胎发生。 为了更深入地了解这一簇在发育和人类疾病中的作用，研究者提出了两种转基因大鼠模型：一种是普遍存在的转基因大鼠（UBC-miR-15/16），其在慢病毒载体中使用人泛素C启动子（UBC）在所有组织中表达miR-15/16;第二种是四环素（泰特）诱导的转基因大鼠（Tet-miR-15/16），其中miR-15/16簇将由泰特调控的慢病毒载体驱动。 将Tet-miR-15/16转基因大鼠与转基因大鼠Rosa 26-rtTA-M2杂交，其中反向反式激活因子rtTA-M2由研究者最近在其实验室中产生的普遍存在的启动子Rosa 26驱动，以获得同时表达miR-15/16和rtTA-M2的条件性双转基因大鼠。 miR-15/16簇在该双转基因大鼠中的表达将受到强力霉素的严格控制。 如果UBC-miR-15/16转基因大鼠模型显示胚胎致死表型，则该双转基因大鼠模型将为研究miR-15/16的生物学功能提供替代方法。 研究者将使用分子生物学、组织学和免疫组织化学方法，通过对不同发育阶段的胚胎、出生后和成年大鼠进行基因分型、表型分析，对这些转基因大鼠进行表征。 这两个模型对于研究miR-15/16簇如何参与发育和其他人类疾病的多种信号通路的分子机制具有重要价值。 项目叙述：本研究将构建表达miR-15/16簇的泛在四环素诱导转基因大鼠，以研究其在发育和其他人类疾病中的作用。

项目成果

miRNA and vascular cell movement.

• DOI: 10.1016/j.addr.2011.01.001
• 发表时间: 2011-07-18
• 期刊: ADVANCED DRUG DELIVERY REVIEWS
• 影响因子: 16.1
• 作者: Yue, Junming

Deletion of DGCR8 in VSMCs of adult mice results in loss of vascular reactivity, reduced blood pressure and neointima formation.

成年小鼠VSMC中DGCR8的缺失导致血管反应性丧失，血压降低和新内膜形成。

• DOI: 10.1038/s41598-018-19660-z
• 发表时间: 2018-01-23
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Zou Y;Chen Z;Jennings BL;Zhao G;Gu Q;Bhattacharya A;Cui Y;Yu B;Malik KU;Yue J
• 通讯作者: Yue J

Silencing the double-stranded RNA binding protein DGCR8 inhibits ovarian cancer cell proliferation, migration, and invasion.

• DOI: 10.1007/s11095-013-1219-9
• 发表时间: 2015-03
• 期刊: PHARMACEUTICAL RESEARCH
• 影响因子: 3.7
• 作者: Guo, Yuqi;Tian, Peng;Yang, Chuanhe;Liang, Zhibing;Li, Min;Sims, Michelle;Lu, Lu;Zhang, Zhan;Li, Hongwei;Pfeffer, Lawrence M.;Yue, Junming
• 通讯作者: Yue, Junming

A miR-21 hairpin structure-based gene knockdown vector.

miR-21发夹结构基因敲低载体。

• DOI: 10.1016/j.bbrc.2010.03.047
• 发表时间: 2010-04-09
• 期刊: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
• 影响因子: 3.1
• 作者: Yue, Junming;Sheng, Yi;Ren, Aixia;Penmatsa, Sravya
• 通讯作者: Penmatsa, Sravya

miRNA biogenesis enzyme Drosha is required for vascular smooth muscle cell survival.

miRNA生物发生酶Drosha是血管平滑肌细胞存活所必需的。

• DOI: 10.1371/journal.pone.0060888
• 发表时间: 2013
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Fan P;Chen Z;Tian P;Liu W;Jiao Y;Xue Y;Bhattacharya A;Wu J;Lu M;Guo Y;Cui Y;Gu W;Gu W;Yue J
• 通讯作者: Yue J