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一种用于监测植物体内细胞基因表达的单细胞生物发光成像系统。

A single-cell bioluminescence imaging system for monitoring cellular gene expression in a plant body.

机构信息

Department of Botany, Graduate School of Science, Kyoto University, Kitashirakawa-oiwake-cho, Sakyo-ku, Kyoto, 606-8502 Japan.

出版信息

Plant Cell Physiol. 2013 Dec;54(12):2085-93. doi: 10.1093/pcp/pct131. Epub 2013 Sep 20.

Abstract

Gene expression is a fundamental cellular process and expression dynamics are of great interest in life science. We succeeded in monitoring cellular gene expression in a duckweed plant, Lemna gibba, using bioluminescent reporters. Using particle bombardment, epidermal and mesophyll cells were transfected with the luciferase gene (luc+) under the control of a constitutive [Cauliflower mosaic virus 35S (CaMV35S)] and a rhythmic [Arabidopsis thaliana CIRCADIAN CLOCK ASSOCIATED 1 (AtCCA1)] promoter. Bioluminescence images were captured using an EM-CCD (electron multiply charged couple device) camera. Luminescent spots of the transfected cells in the plant body were quantitatively measured at the single-cell level. Luminescence intensities varied over a 1,000-fold range among CaMV35S::luc+-transfected cells in the same plant body and showed a log-normal-like frequency distribution. We monitored cellular gene expression under light-dark conditions by capturing bioluminescence images every hour. Luminescence traces of ≥50 individual cells in a frond were successfully obtained in each monitoring procedure. Rhythmic and constitutive luminescence behaviors were observed in cells transfected with AtCCA1::luc+ and CaMV35S::luc+, respectively. Diurnal rhythms were observed in every AtCCA1::luc+-introduced cell with traceable luminescence, and slight differences were detected in their rhythmic waveforms. Thus the single-cell bioluminescence monitoring system was useful for the characterization of cellular gene expression in a plant body.

摘要

基因表达是一个基本的细胞过程,表达动态在生命科学中非常重要。我们成功地使用生物发光报告基因监测了浮萍植物 Lemna gibba 中的细胞基因表达。通过粒子轰击,将荧光素酶基因(luc+)转染到表皮和叶肉细胞中,该基因受组成型启动子[Cauliflower mosaic virus 35S(CaMV35S)]和节律性启动子[Arabidopsis thaliana CIRCADIAN CLOCK ASSOCIATED 1(AtCCA1)]的控制。使用 EM-CCD(电子倍增电荷耦合器件)相机拍摄生物发光图像。在单细胞水平上对植物体内转染细胞的发光斑点进行定量测量。在同一植物体内,CaMV35S::luc+转染细胞的发光强度差异在 1000 倍范围内,并呈现出对数正态分布的频率分布。我们通过每小时拍摄生物发光图像来监测光暗条件下的细胞基因表达。在每次监测过程中,都成功获得了叶片中≥50 个单个细胞的发光轨迹。分别在转染 AtCCA1::luc+和 CaMV35S::luc+的细胞中观察到节律性和组成型发光行为。在可追踪发光的每个 AtCCA1::luc+-引入细胞中都观察到昼夜节律,并且检测到它们的节律波形略有差异。因此,单细胞生物发光监测系统可用于表征植物体内的细胞基因表达。

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