Novel Ubiquitin Dependent Pathways Regulating Neural Tube Closure & Placentation

调节神经管闭合的新型泛素依赖性途径

• 批准号: 8446209
• 负责人: Irene E Zohn
• 金额: $ 32.52万
• 依托单位: CHILDREN'S RESEARCH INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-15 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8446209
• 关键词: Address; Affect; Anencephaly; Angelman Syndrome; Apoptosis; Binding; Biochemical; Biological; Biological Assay; Cell physiology; Cells; Congenital Abnormality; Data; Defect; Development; Embryo; Embryonic Development; Fetal Death; Fetal Growth Retardation; Gene Deletion; Genes; Genetic; Genetic Screening; Goals; Human; In Vitro; Lead; Mediating; Molecular; Mono-S; Mus; Mutant Strains Mice; Neural Tube Closure; Neural Tube Defects; Neural Tube Development; Neural tube; Parkinson Disease; Pathway interactions; Pattern; Phenotype; Placenta; Placentation; Play; Post-Translational Protein Processing; Pre-Eclampsia; Pregnancy; Pregnancy Complications; Process; Proteins; Regulation; Role; Spinal Dysraphism; Spontaneous abortion; Syndrome; Testing; Ubiquitin; Ubiquitination; Yeasts; cell type; disability; human disease; in vivo; insight; multicatalytic endopeptidase complex; mutant; novel; null mutation; protein function; public health relevance; research study; trophoblast; ubiquitin ligase; yeast two hybrid system

DESCRIPTION (provided by applicant): Neural tube and placental defects result in severe complications during pregnancy. Neural tube defects including spina bifida and anencephaly are some of the most common morphological birth defects affecting humans resulting in death of the fetus or long-term disability. Defects in development of the placenta can lead to miscarriage, preeclampsia or intrauterine growth restriction. Studies in mouse have demonstrated that both neural tube and placental development require the activity of a large number of genes and we are only beginning to understand how these genes organize into pathways to control development. Additionally, how the activity of these pathways is fine-tuned to more tightly control the strength and duration of protein action remains unknown. Ubiquitination is a posttranslational modification that plays an important role in regulating protein activity. The importance of ubiquitination is illustrated by the numerous human diseases caused by disruption of ubiquitination pathways including Angelmans Syndrome and Parkinson's disease. In spite of the recognized importance of ubiquitination, its role in controlling protein activity during embryonic development is only beginning to become appreciated. We identified a novel ubiquitin ligase that plays a critical role in neural tube closure and placentation. Our goal is to understand how regulation of protein function by this novel ubiquitin ligase regulates development of the neural tube and placenta. Experiments proposed here will characterize the placenta phenotypes in this mouse mutant to provide valuable insight into the pathways regulated. Additionally, we will use biochemical, cell biological and genetic approaches to identify the substrate of the ubiquitin ligase that mediates neural tube and placental defects in our mutant mouse line. These experiments will define the pathways regulated by this novel ubiquitin ligase to control neural tube and placental development.

描述（申请人提供）：神经管和胎盘缺陷导致妊娠期间严重的并发症。神经管缺陷包括脊柱裂和无脑畸形是影响人类最常见的形态学出生缺陷，可导致胎儿死亡或长期残疾。胎盘发育缺陷可导致流产、先兆子痫或宫内生长受限。对小鼠的研究表明，神经管和胎盘的发育都需要大量基因的活动，我们才刚刚开始了解这些基因如何组织成控制发育的途径。此外，如何微调这些途径的活性以更严格地控制蛋白质作用的强度和持续时间仍然未知。泛素化是一种翻译后修饰，在调节蛋白质活性方面起着重要作用。泛素化的重要性由许多由泛素化途径破坏引起的人类疾病（包括Angelmans综合征和帕金森病）说明。尽管人们认识到泛素化的重要性，但它在胚胎发育过程中控制蛋白质活性的作用才刚刚开始得到重视。我们发现了一种新的泛素连接酶，在神经管闭合和胎盘中起关键作用。我们的目标是了解这种新型泛素连接酶如何调节蛋白质功能调节神经管和胎盘的发育。本文提出的实验将表征该小鼠突变体的胎盘表型，从而为调控途径提供有价值的见解。此外，我们将使用生化、细胞生物学和遗传学方法来鉴定在我们的突变小鼠系中介导神经管和胎盘缺陷的泛素连接酶的底物。这些实验将确定由这种新型泛素连接酶调节的控制神经管和胎盘发育的途径。