HOMEOBOX GENE PITX2 EXPRESSION IN STEM CELLS

同源框基因 PITX2 在干细胞中的表达

• 批准号: 6191993
• 负责人: BERNARD G FORGET
• 金额: $ 30.98万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-08-01 至 2000-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6191993
• 关键词: cell differentiation; cell growth regulation; developmental genetics; embryonic stem cell; flow cytometry; gene expression; gene targeting; hematopoiesis; hematopoietic stem cells; homeobox genes; laboratory mouse; tissue /cell culture; transfection /expression vector

Hematopoietic stem cells comprise a very small fraction of bone marrow mononuclear cells, which retain the capacity for self-renewal as well as controlled differentiation into all the cellular elements of the peripheral blood. The molecular signals that confer the stem cell phenotype and the mechanisms that control stem cell proliferation and differentiation are incompletely understood. In preliminary work, we have identify a divergent homeobox gene (Pitx2) that is expressed in murine hematopoietic stem/progenitor cells but not in differentiated cells. Our studies have demonstrated the expression of a novel mRNA isoforms of this gene in hematopoietic stem/progenitor cells and embryonic stem cells. The research goals of this proposal are to establish the role of this gene in hematopoiesis. Specifically, we propose to: characterize the temporal and over-expression of the gene (products) on hematopoietic progenitor cell growth and differentiation in vitro as well as in vivo: study the effects of loss of function of the gene in ES cells carrying targeted disruptions of the gene as well as in various hematopoietic cells expressing a dominant negative version of Pitx2; and characterize the downstream gene targets of Pitx2 as well as the elements that regulate the expression of Pitx2.

造血干细胞包括非常小部分的骨髓单核细胞，其保留自我更新以及受控分化成外周血的所有细胞成分的能力。赋予干细胞表型的分子信号和控制干细胞增殖和分化的机制还不完全清楚。在初步工作中，我们已经确定了一个不同的同源异型盒基因（Pitx 2），在小鼠造血干/祖细胞中表达，但在分化细胞中不表达。我们的研究已经证明了该基因的一种新的mRNA亚型在造血干/祖细胞和胚胎干细胞中的表达。这项研究的目的是确定该基因在造血中的作用。具体而言，我们建议：表征基因的时间和过度表达（产品）体外和体内造血祖细胞生长和分化：研究基因功能丧失对携带基因靶向破坏的ES细胞以及表达Pitx 2显性阴性形式的各种造血细胞的影响;并表征Pitx 2的下游基因靶标以及调控Pitx 2表达的元件。