Molecular Regulation of Mammalian Meiosis

哺乳动物减数分裂的分子调控

• 批准号: 8474281
• 负责人: KENNETH PAIGEN
• 金额: $ 163.06万
• 依托单位: JACKSON LABORATORY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-01 至 2018-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8474281
• 关键词: Address; Alleles; Biological; Biological Process; Biology; Cell division; Cellular biology; Chromosome Mapping; Complex; Computational Technique; DNA; Data Analyses; Defect; Embryo; Experimental Models; Fingers; Gametogenesis; Genes; Genetic; Genetic Recombination; Genetic Transcription; Genomics; Goals; Human; Hybrids; Infertility; Inheritance Patterns; Instruction; Location; Meiosis; Modeling; Molecular; Molecular Biology; Mus; Nature; Play; Population Genetics; Preparation; Process; Protein Chemistry; Proteins; Regulation; Reproductive Health; Role; Specificity; Spermatocytes; Sterility; Structure; Transcriptional Activation; animal resource; data management; egg; human disease; insight; mutant; programs; research study; sperm cell

DESCRIPTION (provided by applicant): Despite the biological importance of mammalian meiosis, several of its significant features rema n largely unexplained. Recent discoveries by ourselves and others have shown that many of these features are controlled by the same protein, PRDM9. Our long-term objective is to determine how these controls are related, how they are achieved, and how PRDM9 fits into the larger network of proteins controlling meiosis progression. This will be greatly facilitated by the availability of multiple PRDM9 alleles in mice, each with its own regulatory specificities expressed in the most useful mammalian experimental model that we have. PRDM9 is an exceptional protein in the diversity of biological functions it carries out, in its unusual domain structure, and in its diverse molecular activities. The insights this study will provide extend beyond meiosis to major aspects of population genetics, as the location of hotspots determines patterns of inheritance; to genetic mapping studies identifying human disease genes; and to evolutionary biology, as allelic incompatibilities in PRDM9 can produce hybrid sterility. To address the relevant experimental questions, we have organized a coordinated effort among four projects representing diverse experimental approaches: genetics (Project A), protein chemistry (Project B), computational integration (Project 0), cell biology (Project D), and molecular biology (Projects A, B, C and D). Our Animal Resources Core will provide mice and new mutant strains. A Cell Biology Core will provide preparations of spermatocytes and assist in ChIP experiments. The Computational Core will perform data management and analysis. Our long-term objectives derive from the following overall program goals: a) Comprehensively define PRDM9's regulatory functions in recombination, transcription, and gametogenesis; b) Define the role of PRDM9 in regulation of meiosis by identifying and characterizing its interactions with genomic DNA, other meiotic proteins, and specialized meiotic structures; c) Define the overall role of PRDM9 in gametogenesis, hotspot activation, and transcription by using computational techniques to build an integrated model of its molecular functions; and d) Exploit the exceptional degree of variability in the Zn fingers (ZNF) of PRDM9 to clarify the complex nature of ZNF - DNA interactions, which are so ubiquitous in genomic regulation. Results of the program project will significantly increase the understanding of the mechanisms that regulate meiosis as well as their involvement in other important biological processes.

描述（由申请人提供）： 尽管哺乳动物减数分裂在生物学上具有重要意义，但它的几个重要特征仍然很大程度上无法解释。我们和其他人最近的发现表明，许多这些特征都是由同一种蛋白质PRDM 9控制的。我们的长期目标是确定这些控制是如何相关的，它们是如何实现的，以及PRDM 9如何适应控制减数分裂进程的蛋白质的更大网络。这将极大地促进了小鼠中多个PRDM 9等位基因的可用性，每个等位基因在我们拥有的最有用的哺乳动物实验模型中表达了其自身的调节特异性。PRDM 9是一种特殊的蛋白质，其生物学功能的多样性，其不寻常的结构域结构，以及其多样的分子活性。这项研究提供的见解将超越减数分裂扩展到群体遗传学的主要方面，因为热点的位置决定了遗传模式;遗传图谱研究确定了人类疾病基因;进化生物学，因为PRDM 9中的等位基因不相容性可以产生杂交不育。为了解决相关的实验问题，我们组织了四个代表不同实验方法的项目的协调努力：遗传学（项目A），蛋白质化学（项目B），计算集成（项目0），细胞生物学（项目D）和分子生物学（项目A，B，C和D）。我们的动物资源中心将提供小鼠和新的突变品系。细胞生物学核心将提供精母细胞的准备工作，并协助ChIP实验。计算核心将执行数据管理和分析。我们的长期目标源自以下总体计划目标：a）全面定义PRDM 9在重组、转录和配子发生中的调节功能; B）通过识别和表征PRDM 9与基因组DNA、其他减数分裂蛋白和特殊减数分裂结构的相互作用，定义PRDM 9在减数分裂调节中的作用; c）通过使用计算技术建立其分子功能的整合模型，定义PRDM 9在配子发生、热点激活和转录中的总体作用;和d）利用PRDM 9的锌指（ZNF）中异常程度的变异性来阐明ZNF-DNA相互作用的复杂性质，其在基因组调控中如此普遍存在。该计划项目的结果将显着增加对调节减数分裂及其参与其他重要生物过程的机制的理解。