Genomic Fate Maps

基因组命运图谱

• 批准号: 8215841
• 负责人: MARSHALL S. HORWITZ
• 金额: $ 32.49万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-02-01 至 2015-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8215841
• 关键词: Achievement; Address; Affect; Anatomy; Animal Model; Back; Biology; Birth Records; Caenorhabditis elegans; Cataloging; Catalogs; Cell Count; Cell Line; Cells; Central Vein; Cessation of life; Chemicals; Collaborations; Computer-Assisted Three-Dimensional Imaging; DNA biosynthesis; Development; Developmental Biology; Devices; Disease; Dissection; Drops; Dyes; Embryo; Ethylnitrosourea; Frequencies; Gene Expression; Genetic Markers; Genetic Recombination; Genome; Genomics; Goals; Hepatic; Hepatocyte; Individual; Inherited; Injury; Knowledge; Label; Length; Letters; Life; Liver; Mammalian Cell; Mammals; Maps; Methods; Microdissection; Microscope; Microtome - medical device; Mismatch Repair; Molecular; Mus; Mutagenesis; Mutation; NCI Center for Cancer Research; Organ; Organism; Phylogenetic Analysis; Population; Positioning Attribute; Recording of previous events; Repetitive Sequence; Resolution; Sampling; Somatic Mutation; Stem cells; Stream; System; Techniques; Technology; Time; Tissues; Trees; Validation; base; distraction; in vivo; laser capture microdissection; novel; progenitor; research study; tissue regeneration; zygote

DESCRIPTION (provided by applicant): Recent, surprising, and controversial discoveries have challenged conventional concepts regarding the origins and plasticity of stem cells, and their contributions to tissue regeneration, and highlight just how little is known about mammalian development in comparison to simpler model organisms. In the case of the transparent worm, C. elegans, Sulston and colleagues used a microscope to record the birth and death of every cell during its life, and the compilation of this fate maps represents a milestone achievement of developmental biology. Determining a fate map for mammals or other higher organisms is more complicated, because they are opaque, take a long time to mature, and have a tremendous number of cells. Consequently, fate mapping experiments have relied on tagging a progenitor cell with a dye or genetic marker in order to later identify its descendants. This approach, however, extracts little information, because it only reveals that a population of cells, all inheriting the same label, share a common ancestor but tells nothing of how each cell is related to one another. To avoid that, as well as the technical limitations of current methods for mapping cell fate, we propose a new strategy for retrospectively deriving cell fate maps by using phylogenetics to infer the order in which somatic mutations have arisen in the genomes of individual cells during the development of multicellular organisms. DNA replication introduces mutations, particularly at repetitive sequences, every time a cell divides. In Preliminary Studies we demonstrate that cataloging the frequent mutations affecting the length of polyguanine tracts allows for deducing the history of mouse cells either passaged in culture or sampled from the various tissues of a single individual. Toward an ultimate goal of constructing a high resolution mammalian cell fate map, we plan three Specific Aims: 1. Compare phylogenetic fate maps to conventional fate maps derived from genetically marked mice. 2. Advance the technology of this approach. 3. Successively build a liver cell fate map in order to address controversies regarding the clonal, embryonic, and anatomic origins of hepatic stem cells during development and in disease.A goal of biology is to understand how a single cell divides and gives rise to all the different tissues and organs in the body. Fate maps describe how cells within an individual are related to one another and can be likened to a tree of life, in which the origin of a particular cell can be traced back through its progenitors to the fertilized egg. We propose a new method for exploring developmental biology by constructing fate maps based on distinctive mutations inevitably accumulating in the genome each time a cell divides. We will initially focus our studies on how the liver develops and responds to injury.

描述（由申请人提供）：最近，令人惊讶的和有争议的发现已经挑战了关于干细胞的起源和可塑性及其对组织再生的贡献的传统概念，并突出了与更简单的模型生物体相比，对哺乳动物发育的了解是多么少。在透明蠕虫的情况下，C. Sulston及其同事使用显微镜记录了每个细胞在其生命过程中的出生和死亡，这一命运图的编制代表了发育生物学的里程碑式成就。确定哺乳动物或其他高等生物的命运图更为复杂，因为它们是不透明的，需要很长时间才能成熟，并且有大量的细胞。因此，命运定位实验依赖于用染料或遗传标记标记祖细胞，以便以后识别其后代。然而，这种方法提取的信息很少，因为它只揭示了一个细胞群体，所有继承相同的标签，共享一个共同的祖先，但没有告诉每个细胞是如何相互关联的。为了避免这一点，以及目前绘制细胞命运的方法的技术局限性，我们提出了一种新的策略，通过使用多细胞遗传学来推断在多细胞生物的发育过程中个体细胞的基因组中体细胞突变出现的顺序，来回顾性地推导细胞命运图。每当细胞分裂时，DNA复制都会引入突变，特别是在重复序列上。在初步研究中，我们证明，编目的频繁突变影响的长度的聚鸟嘌呤束允许推导的历史，小鼠细胞在培养中传代或从一个单一的个人的各种组织取样。为了构建一个高分辨率的哺乳动物细胞命运图的最终目标，我们计划了三个具体目标：1。比较系统发育的命运地图传统的命运地图来自遗传标记的小鼠。2.推进这种方法的技术。3.成功地建立了肝细胞命运图，以解决有关肝干细胞在发育和疾病中的克隆，胚胎和解剖起源的争议。生物学的目标是了解单个细胞如何分裂并产生体内所有不同的组织和器官。命运图描述了一个人体内的细胞是如何相互关联的，可以比作一棵生命之树，其中特定细胞的起源可以通过其祖细胞追溯到受精卵。我们提出了一种探索发育生物学的新方法，即根据细胞每次分裂时不可避免地在基因组中积累的独特突变构建命运图。我们最初将重点研究肝脏如何发育和对损伤的反应。