A technique enabling the controlled gene expression in targeted single cells of C. elegans

M. Suzuki, Y. Kamei, S. Yuba, S. Takagi
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引用次数: 3

Abstract

Usually, tissue specific promoters are used to examine the function of a gene of interest in vivo in transgenic lines of model organisms such as C. elegans and mice, complementing the genetic analysis with mosaic organisms. However, use of tissue specific promoters is limited by their inherent properties to drive gene expression in a restricted temporal-spatial expression pattern. It is desirable to develop techniques for regulating gene expression in a controllable way both temporally and spatially at single cell resolution. Once such techniques have been established in model organisms, they would serve as a basis for developing techniques to manipulate cellular behavior in other organisms including human. In this paper, we will first summarize previous attempts to drive gene expression at a desired time and space by using inducible promoters, in particular heat shock promoters. Then, we examine problems encountered in the previous attempts, and report our new approach to circumvent them
秀丽隐杆线虫单细胞控制基因表达的技术
通常,组织特异性启动子用于在秀丽隐杆线虫和小鼠等模式生物的转基因系中检测感兴趣的基因在体内的功能,并与马赛克生物的遗传分析相补充。然而,组织特异性启动子的使用受到其内在特性的限制,无法在有限的时空表达模式中驱动基因表达。在单细胞分辨率下,开发一种时间和空间可控的基因表达调节技术是很有必要的。一旦这些技术在模式生物中建立起来,它们将作为开发技术的基础,以操纵包括人类在内的其他生物的细胞行为。在本文中,我们将首先总结以往使用诱导启动子,特别是热休克启动子在期望的时间和空间驱动基因表达的尝试。然后,我们检查在以前的尝试中遇到的问题,并报告我们规避它们的新方法
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