MOLECULAR GENETICS OF PROGRESSIVE OSSEOUS HETEROPLASIA

进行性骨异质发育的分子遗传学

基本信息

批准号：
7924441
负责人：
EILEEN M SHORE
金额：
$ 10.9万
依托单位：
UNIVERSITY OF PENNSYLVANIA
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-09-18 至 2010-09-17
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7924441
关键词：
Adipocytes Alleles Applications Grants Bone Diseases Cell Differentiation process Cell Line Cell Surface Receptors Cell physiology Cells Characteristics Childhood Complex Couples DNA DNA Methylation DNA Sequence Dependence Diagnostic Fatty acid glycerol esters Foundations Future GNAS gene GTP-Binding Protein alpha Subunits, Gs Gene Expression Gene Mutation Gene Silencing Genes Genetic Polymorphism Genomics Goals Hereditary Disease Heterotopic Ossification Human Inherited Intracellular Second Messenger Investigation Knockout Mice Location Methylation Molecular Genetics Mono-S Mus Mutate Mutation Mutation Detection Nomenclature Osteoblasts Osteogenesis Pathway interactions Patients Pattern Phenotype Proteins Regulation Research Personnel Reverse Transcriptase Polymerase Chain Reaction Role Second Messenger Systems Signal Transduction Site-Directed Mutagenesis Skeletal Muscle Skin Staging Stem cells Time Tissues Transcript United States National Institutes of Health Work adipocyte differentiation bone bone cell embryonic stem cell homologous recombination imprint insight lipid biosynthesis mRNA Expression mutant osteoblast differentiation precursor cell programs promoter research study restriction enzyme subcutaneous treatment strategy

项目摘要

DESCRIPTION (provided by applicant): Genetic disorders of osteogenesis provide valuable insight into the regulation of bone formation. Progressive osseous heteroplasia (POH) is a rare and disabling genetic disorder in which the body produces bone in skin, fat and skeletal muscle. Gene mutations in POH patients inactivate one of the two copies of the GNAS gene and alter the fate of cells to cause bone formation in inappropriate locations (heterotopic ossification). GNAS encodes the G(s)alpha protein, which couples signaling via cell surface receptors to intracellular second messengers, however the specific effects of these mutations on bone cell differentiation are unknown. Ectopic bone formation in POH patients often arises within subcutaneous fat, suggesting a close, perhaps reciprocal, relationship between bone and fat cell differentiation. In addition to continuing investigations of GNAS inheritance and expression in POH, a primary goal of this proposal is to examine the effects of heterozygous inactivating GNAS mutations on bone (osteoblast) and fat (adipocyte) cell differentiation. We hypothesize that: (1) Heterozygous inactivating mutation of the GNAS gene alters cellular signaling that directs osteoblast and/or adipocyte differentiation, and (2) The complex phenotypic consequences of inactivating GNAS mutations are influenced by maternal/paternal inheritance of GNAS. The following Specific Aims will be conducted: 1. Investigate the parental origin of the GNAS allele that carries GNAS mutations in POH patients. 2. Examine POH genomic DNA for methylation characteristic of imprinting at the GNAS locus. 3. Examine the differential expression of GNAS mRNAs during osteoblast and adipocyte differentiation. 4. Examine the effects of heterozygous GNAS gene inactivation on osteoblast and adipocyte differentiation. 5. Investigate the effects of an inactive GNAS gene on expression of specific GNAS transcripts during osteoblast and adipocyte differentiation. The overall goal of this project is to characterize the role of the GNAS gene in the regulation of bone cell differentiation. The studies described in this proposal will provide the foundation to examine the specific pathways through which GNAS regulates osteogenesis. These investigations will provide important information for developing diagnostic and treatment strategies for a wide range of disorders of bone such as POH and more common conditions.

描述（由申请人提供）：成骨的遗传疾病为调节骨形成提供了宝贵的见解。进行性骨性异质（POH）是一种罕见且残疾的遗传疾病，人体在皮肤，脂肪和骨骼肌中产生骨骼。 POH患者的基因突变使GNA基因的两个副本之一失活，并改变了细胞的命运以在不适当的位置引起骨形成（异位骨化）。 GNA编码G（s）α蛋白，该蛋白通过细胞表面受体的信号传导与细胞内第二使者，但是这些突变对骨细胞分化的特定影响尚不清楚。 POH患者的异位骨形成通常发生在皮下脂肪中，表明骨与脂肪细胞分化之间的关系很近，可能是相互的。除了对POH中的GNA遗传和表达的持续研究外，该建议的主要目标是检查杂合灭活GNA突变对骨（成骨细胞）和脂肪（脂肪细胞）细胞分化的影响。我们假设：（1）GNA基因的杂合灭活突变改变了指导成骨细胞和/或脂肪细胞分化的细胞信号传导，以及（2）灭活GNAS突变的复杂表型后果受母体/父亲/父亲的gnas遗传的影响。将进行以下具体目的：1。研究POH患者携带GNA突变的GNA等位基因的父母来源。 2。检查POH基因组DNA，以了解GNA基因座的印迹的甲基化特征。 3。检查成骨细胞和脂肪细胞分化过程中GNAS mRNA的差异表达。 4。检查杂合子GNA基因失活对成骨细胞和脂肪细胞分化的影响。 5。研究非活性GNA基因对成骨细胞和脂肪细胞分化过程中特定GNA转录本的表达的影响。该项目的总体目标是表征GNA基因在调节骨细胞分化中的作用。该提案中描述的研究将为检查GNA调节成骨的特定途径提供基础。这些调查将为开发诊断和治疗策略的重要信息，以针对POH等多种骨骼疾病以及更常见的疾病。