Functional characterization of piRNPs
Functional characterization of piRNPs
批准号:
8598479
负责人:
ZISSIMOS MOURELATOS
金额:
$38.49万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-03-01 至 2015-02-12
关键词:
AddressAffectAnimalsArginineAubergineBinding ProteinsBiochemicalBiogenesisBiological ModelsChIP-seqComplexComputer AnalysisDataDevelopmentDiseaseDrosophila genusDrosophila melanogasterEnzymatic BiochemistryGene Expression RegulationGenesGeneticGermGerm CellsHomologous GeneHouse miceIn VitroKnowledgeLeadLightMediatingMethodsMethylationMicroRNAsModificationMusOrganismPathway interactionsPost-Translational Protein ProcessingPostdoctoral FellowPropertyProtein BindingProtein FamilyProtein-Arginine N-MethyltransferaseProteinsRNARNA HelicaseReagentReproductionResearch PersonnelResearch SupportRibonucleoproteinsRoleScientistSmall RNAStem cellsStructureTransgenic OrganismsUniversitiesWorkcofactorexperiencein vivoinsightmemberpiRNAprogramsprotein functionprotein protein interactionpublic health relevanceresearch studystem cell biologytranscriptome sequencing
中文摘要
描述(由申请人提供):随着小rna编程的核糖核蛋白(RNP)复合物的发现,我们对基因表达调控的理解发生了根本性的变化。这些复合物的核心是Argonaute蛋白家族的成员,该家族由两个亚支组成:Ago和Piwi。蛋白质与microrna结合。Piwi蛋白与Piwi相互作用rna (piRNAs)结合。Piwi蛋白对生殖系发育和生殖细胞分化至关重要。然而,许多pirna和Piwi蛋白的功能和RNA靶点在很大程度上是未知的。对黑腹果蝇的遗传研究已经确定了母体基因,其产物在称为种质的结构中组装,这是生殖细胞规范所必需的。这些因子包括piRNA结合蛋白Aubergine,精氨酸蛋白甲基转移酶(PRMT5)及其辅助因子Tudor蛋白和Vasa RNA解旋酶。虽然果蝇的种质组装遗传途径已被很好地描述,但种质蛋白的关系和功能尚不清楚。胚质中也含有rna,它们被认为是生殖细胞特化的必要成分,但其身份大多是未知的。果蝇生殖系发育和生殖细胞规范所需的大多数基因在其他动物(如小鼠)的生殖系中具有进化保守作用。我们的研究正在揭示关键种质成分的重要关系和功能。我们发现由PRMT5催化的Piwi蛋白精氨酸甲基化是一种进化保守的修饰,介导与Tudor蛋白的相互作用。我们还发现Vasa及其小鼠同源物含有甲基化精氨酸。在Aim 1中,我们将对黑腹果蝇的piRNP复合物及其RNA靶点进行功能表征。在Aim 2中,我们将在小家鼠中对piRNP复合物及其RNA靶点进行功能表征。研究这两种生物将突出piRNP功能和生殖细胞规范和发育的保守作用和途径,但也可能揭示物种特异性功能。本提案中详细的研究将解决piRNPs和相关蛋白及其RNA靶点功能的基本方面,以及这些因素在生殖细胞规范和种系发育中的作用。
英文摘要
DESCRIPTION (provided by applicant): Our understanding of gene expression regulation has changed radically with the discovery of ribonucleoprotein (RNP) complexes programmed with small RNAs. At the core of these complexes are members of the Argonaute family of proteins that is comprised of two subclades: Ago and Piwi. Ago proteins bind to microRNAs. Piwi proteins bind to piwi-interacting RNAs (piRNAs). Piwi proteins are essential for germline development and germ cell specification. However, the function and RNA targets for many piRNAs and Piwi proteins are largely unknown. Genetic studies in Drosophila melanogaster have identified maternal genes whose products assemble in structures known as germ plasm, and which are required for germ cell specification. Among these factors are the piRNA binding protein Aubergine, an arginine protein methyltransferase (PRMT5) and its cofactor, the Tudor protein and the Vasa RNA helicase. Although the genetic pathway of germ plasm assembly has been well characterized in Drosophila, the relationship and functions of germ plasm proteins is not well understood. Germ plasm also contains RNAs, that are thought to be essential for germ cell specification but whose identities are mostly unknown. Most of the genes that are required for germline development and germ cell specification in Drosophila have evolutionary conserved roles in the germline of other animals, such as mice. Our studies are uncovering important relationships and functions of critical germ plasm components. We find that arginine methylation of Piwi proteins, catalyzed by PRMT5, is an evolutionary conserved modification that mediates interaction with Tudor proteins. We also find that Vasa and its mouse homolog, contain methylated arginines. In Aim 1, we will functionally characterize piRNP complexes and their RNA targets in Drosophila melanogaster. In Aim 2, we will functionally characterize piRNP complexes and their RNA targets in Mus musculus. Studying both organisms will highlight conserved roles and pathways for piRNP function and germ cell specification and development, but will also likely uncover species-specific functions. The studies detailed in this proposal will address fundamental aspects of the function of piRNPs and associated proteins and their RNA targets, and the role of these factors in germ cell specification and germline development.
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