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绿色荧光蛋白作为植物细胞中的一种新型活体标记物。

Green-fluorescent protein as a new vital marker in plant cells.

作者信息

Sheen J, Hwang S, Niwa Y, Kobayashi H, Galbraith D W

机构信息

Department of Molecular Biology, Massachusetts General Hospital, Boston, USA.

出版信息

Plant J. 1995 Nov;8(5):777-84. doi: 10.1046/j.1365-313x.1995.08050777.x.

Abstract

The green-fluorescent protein (GFP) from jellyfish Aequorea victoria has been used as a convenient new vital marker in various heterologous systems. However, it has been problematic to express GFP in higher eukaryotes, especially in higher plants. This paper reports that either a strong constitutive or a heat-shock promoter can direct the expression of GFP which is easily detectable in maize mesophyll protoplasts. In this single-cell system, bright green fluorescence emitted from GFP is visible when excited with UV or blue light even in the presence of blue fluorescence from the vacuole or the red chlorophyll autofluorescence from chloroplasts using a fluorescence microscope. No exogenous substrate, co-factor, or other gene product is required. GFP is very stable in plant cells and shows little photobleaching. Viable cells can be obtained after fluorescence-activated cell sorting based on GFP. The paper further reports that GFP can be detected in intact tissues after delivering the constructs into Arabidopsis leaf and root by microprojectile bombardment. The successful detection of GFP in plant cells relies on the use of a universal transcription enhancer from maize or the translation enhancer from tobacco mosaic virus (TMV) to boost the expression. This new reporter could be used to monitor gene expression, signal transduction, co-transfection, transformation, protein trafficking and localization, protein-protein interaction, cell separation and purification, and cell lineage in higher plants.

摘要

来自维多利亚多管水母的绿色荧光蛋白(GFP)已在各种异源系统中作为一种便捷的新型活体标记物使用。然而,在高等真核生物中,尤其是在高等植物中表达GFP一直存在问题。本文报道,强组成型启动子或热休克启动子均可指导GFP的表达,在玉米叶肉原生质体中易于检测到。在这个单细胞系统中,即使存在来自液泡的蓝色荧光或来自叶绿体的红色叶绿素自发荧光,使用荧光显微镜在紫外光或蓝光激发下,GFP发出的亮绿色荧光仍清晰可见。无需外源底物、辅因子或其他基因产物。GFP在植物细胞中非常稳定,几乎没有光漂白现象。基于GFP进行荧光激活细胞分选后可获得活细胞。本文还报道,通过微粒轰击将构建体导入拟南芥叶片和根后,在完整组织中可检测到GFP。在植物细胞中成功检测到GFP依赖于使用来自玉米的通用转录增强子或来自烟草花叶病毒(TMV)的翻译增强子来促进表达。这种新的报告基因可用于监测高等植物中的基因表达、信号转导、共转染、转化、蛋白质运输和定位、蛋白质-蛋白质相互作用、细胞分离和纯化以及细胞谱系。

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