Germ cell specifications and differentiation in planarians.

涡虫的生殖细胞规格和分化。

• 批准号: 8843275
• 负责人: Phillip A Newmark
• 金额: $ 24.29万
• 依托单位: UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-01-09 至 2016-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8843275
• 关键词: Address; Adult; Amaze; Animal Model; Animals; Biology; Cell Differentiation process; Cell Lineage; Cells; Chromatin; Contraceptive methods; Cues; Data; Development; Double-Stranded RNA; Embryo; Embryonic Development; Ensure; Environment; Environmental Risk Factor; Fresh Water; Gene Expression; Gene Targeting; Generations; Genes; Genetic Materials; Genetic Models; Genetic Transcription; Genomic approach; Germ Cells; Germ cell tumor; Goals; Human; In Situ Hybridization; Individual; Infertility; Invertebrates; Knowledge; Laboratories; Link; Malignant Neoplasms; Mammals; Mediating; Meiosis; Modeling; Mus; Natural regeneration; Nature; Neuropeptide Receptor; Neuropeptides; Nutritional; Organism; Parents; Physiological; Planarians; Platyhelminths; Play; Population; Post-Transcriptional Regulation; Precipitation; Protein Isoforms; RNA Interference; Regulation; Reproductive system; Research; Resources; Role; Signal Transduction; Specific qualifier value; Stem cells; Study models; Tissues; To specify; Undifferentiated; United States National Institutes of Health; Work; adult stem cell; base; cell type; combat; egg; feeding; functional genomics; gene discovery; gene function; gene repression; genome-wide; genomic tools; innovation; neuronal cell body; neuropeptide Y; neurotransmission; next generation; next generation sequencing; novel strategies; nuclear factor Y; offspring; peptide hormone; receptor; regenerative; research study; response; sex; sperm cell; transcription factor

DESCRIPTION (provided by applicant): Germ cells serve as a link between generations, producing gametes that propagate genetic material from parent to offspring. Understanding the mechanisms by which germ cells develop will help illuminate the nature of totipotency, the causes of infertility, and the origins of germ cell tumors. Much knowledge of germ cell development derives from studying model organisms that utilize cytoplasmic determinants to specify germ cell fate in early embryogenesis. In contrast, many organisms (including mammals) utilize inductive signals to specify germ cell fate later in development. In spite of these differences, germ cells specified by determinants and those formed inductively share several common intrinsic mechanisms, including transcriptional repression of somatic fates and post-transcriptional control of gene expression. Mechanistic studies of inductive germ cell development have been limited almost exclusively to mouse and important questions remain unanswered. For example, what transcriptional networks define and maintain germ cell fate? After a germ cell has been specified, what systemic factors link its further differentiation with te physiological status of the animal? The freshwater planarian, Schmidtea mediterranea, serves as a powerful model for studying these questions. It has prodigious regenerative abilities, based upon a population of adult stem cells that allow even tiny body fragments to regenerate complete individuals. In planarians, the germ cell lineage develops post- embryonically from the somatic stem cells; like the soma, the germ cell lineage can also be regenerated. Preliminary data generated in the applicant's laboratory have identified intrinsic and extrinsic regulators required for maintaining germ cells and for regulating their differentiation. Based on these data, two specific aims will be pursued: (i) to characterize the transcriptional network in early germ cells; and (ii) to dissect the neuropeptide-based systemic regulation of germ cell differentiation. Work performed under the first aim will use chromatin immuno-precipitation, next-generation sequencing, and computational approaches to identify targets of a germ cell-specific transcription factor required for maintaining early germ cells. Experiments conducted under aim two will characterize the neuropeptide receptor mediating the systemic regulation of germ cell development, identify the cell type(s) that express the receptor, and discover genes expressed in response to neuropeptide signaling. For both aims, the functional genomic tools for studying S. mediterranea (high- throughput in situ hybridization; RNA interference by feeding double-stranded RNA) will be used to validate target genes and determine their functions. These studies use a model organism with unique attributes, and take unbiased, genomic approaches to identify conserved factors; thus, they have great potential to innovate. This work is significan because of its potential: (i) to identify conserved genes required for proper germ cell development; and (ii) to provide a promising strategy for understanding and treating parasitic flatworms that infect hundreds of millions of people worldwide.

描述（由申请人提供）：生殖细胞作为世代之间的联系，产生配子，将遗传物质从亲本繁殖到后代。了解生殖细胞发育的机制将有助于阐明全能性的本质、不育的原因和生殖细胞肿瘤的起源。生殖细胞发育的许多知识来自于研究利用细胞质决定因素来指定早期胚胎发生中生殖细胞命运的模式生物。相反，许多生物（包括哺乳动物）利用诱导信号来指定生殖细胞在发育后期的命运。尽管存在这些差异，但由决定因素指定的生殖细胞和诱导形成的生殖细胞具有几种共同的内在机制，包括体细胞命运的转录抑制和基因表达的转录后控制。诱导生殖细胞发育的机制研究几乎仅限于小鼠，重要的问题仍然没有答案。例如，什么样的转录网络定义和维持生殖细胞的命运？指定生殖细胞后，哪些系统因素将其进一步分化与动物的生理状态联系起来？淡水真涡虫，Schmidtea medialacea，是研究这些问题的有力模型。它具有惊人的再生能力，基于一群成年干细胞，即使是微小的身体碎片也能再生完整的个体。在真涡虫中，生殖细胞谱系从体干细胞胚胎后发育;像索马一样，生殖细胞谱系也可以再生。在申请人的实验室中产生的初步数据已经确定了维持生殖细胞和调节其分化所需的内在和外在调节剂。基于这些数据，将追求两个具体的目标：（i）在早期生殖细胞的转录网络的特点;（ii）解剖生殖细胞分化的神经肽为基础的系统性调节。 在第一个目标下进行的工作将使用染色质免疫沉淀，下一代测序和计算方法来确定维持早期生殖细胞所需的生殖细胞特异性转录因子的靶点。根据目标二进行的实验将表征介导生殖细胞发育的系统调节的神经肽受体，鉴定表达受体的细胞类型，并发现响应神经肽信号传导而表达的基因。为了这两个目标，研究S. medioprotea（高通量原位杂交;通过喂养双链RNA进行RNA干扰）将用于验证靶基因并确定其功能。这些研究使用具有独特属性的模式生物，并采用无偏见的基因组方法来识别保守因子;因此，它们具有很大的创新潜力。这项工作是有意义的，因为它的潜力：（i）确定适当的生殖细胞发育所需的保守基因;和（ii）提供一个有前途的战略，了解和治疗寄生扁形虫感染数亿人在世界各地。