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OPTOGENETIC CONTROL METHOD FOR PROLIFERATION AND DIFFERENTIATION OF STEM CELLS

机译:干细胞增殖和分化的光控制方法

摘要

Using an optogenetic gene expression regulation system, the present invention provides a method for controlling, by using light irradiation to regulate the expression of factors that determine neural differentiation, whether to proliferate and maintain neural precursor cells (NPC), or whether to induce differentiation of neural stem cells into nervous system cells. The present invention is based on: the discovery that neural differentiation factors such as Ascl1, Hes1, and Olig2 are expressed in NPCs periodically in an oscillatory manner but that the expression of any one of these becomes dominant during fate determination; and the structure of gene expression systems in which a target gene can be expressed periodically in an oscillatory manner. In other words, the present invention provides a method for either oscillating the expression of a target factor and maintaining and amplifying NPCs, or inducing sustained expression of the target factor and inducing differentiation into committed nervous system cells by said factor, said method being accomplished by introducing, into NPCs, a nucleic acid which codes a transcriptional activator (GAL4-Vivid-p65 fusion protein; GAVPO) that is activated (dimerized) in response to blue light, and a nucleic acid which links DNA, which codes a target neural differentiation determining factor downstream of a promoter that includes a cis sequence to which the transcriptional activator binds, and a 3'-UTR, which destabilizes mRNA, and by irradiating the NPCs with blue light for short periods of time, changing the cycle.
机译:使用光遗传基因表达调节系统,本发明提供了一种方法,该方法通过使用光辐射调节决定神经分化的因子的表达,是否增殖和维持神经前体细胞(NPC)或是否诱导其分化来进行控制。神经干细胞转变为神经系统细胞。本发明基于以下发现:发现神经分化因子例如Ascl1,Hes1和Olig2在NPC中周期性地以振荡的方式表达,但是在命运决定期间这些表达中的任何一种都占主导。以及可以以振荡方式周期性地表达靶基因的基因表达系统的结构。换句话说,本发明提供了一种用于振荡靶标因子的表达并维持和扩增NPC,或通过所述因子诱导靶标因子的持续表达并诱导分化为定殖神经系统细胞的方法,所述方法通过向NPC中引入编码转录激活剂(GAL4-Vivid-p65融合蛋白; GAVPO)的核酸,该转录激活剂响应蓝光而被激活(二聚化),以及连接DNA的核酸,编码目标神经分化启动子下游的决定因子,其包括转录激活因子所结合的顺式序列和使mRNA不稳定的3'-UTR,并通过短时间用蓝光照射NPC来改变循环。

著录项

  • 公开/公告号WO2015041219A1

    专利类型

  • 公开/公告日2015-03-26

    原文格式PDF

  • 申请/专利权人 KYOTO UNIVERSITY;

    申请/专利号WO2014JP74458

  • 申请日2014-09-17

  • 分类号C12N5/10;C12N5/0797;C12N15/09;C07K19;

  • 国家 WO

  • 入库时间 2022-08-21 15:07:37

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