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通过流式细胞术分析出芽酵母细胞周期

Analysis of the Budding Yeast Cell Cycle by Flow Cytometry.

作者信息

Rosebrock Adam P

机构信息

Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada.

出版信息

Cold Spring Harb Protoc. 2017 Jan 3;2017(1):2017/1/pdb.prot088740. doi: 10.1101/pdb.prot088740.

Abstract

DNA synthesis is one of the landmark events in the cell cycle: G cells have one copy of the genome, S phase cells are actively engaged in DNA synthesis, and G cells have twice as much nuclear DNA as G cells. Cellular DNA content can be measured by staining with a fluorescent dye followed by a flow-cytometric readout. This method provides a quantitative measurement of cell cycle position on a cell-by-cell basis at high speed. Using flow cytometry, tens of thousands of single-cell measurements can be generated in a few seconds. This protocol details staining of cells of the budding yeast Saccharomyces cerevisiae for flow cytometry using Sytox Green dye in a method that can be scaled widely-from one sample to many thousands and operating on inputs ranging from 1 million to more than 100 million cells. Flow cytometry is preferred over light microscopy or Coulter analyses for the analysis of the cell cycle as DNA content and cell cycle position are being directly measured.

摘要

DNA合成是细胞周期中的标志性事件之一:G期细胞有一份基因组拷贝,S期细胞积极参与DNA合成,而G期细胞的核DNA是G期细胞的两倍。细胞DNA含量可以通过用荧光染料染色后进行流式细胞仪读数来测量。该方法能在逐个细胞的基础上高速定量测量细胞周期位置。使用流式细胞仪,几秒内就能生成数万个单细胞测量数据。本方案详细介绍了使用Sytox Green染料对出芽酵母酿酒酵母细胞进行染色以用于流式细胞仪分析的方法,该方法可广泛扩展——从一个样本到数千个样本,并且适用于100万个到超过1亿个细胞的输入量。对于细胞周期分析,流式细胞仪比光学显微镜或库尔特分析更受青睐,因为它能直接测量DNA含量和细胞周期位置。

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