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利用流式细胞术估算植物细胞核DNA含量

Estimation of nuclear DNA content in plants using flow cytometry.

作者信息

Dolezel Jaroslav, Greilhuber Johann, Suda Jan

机构信息

Laboratory of Molecular Cytogenetics and Cytometry, Institute of Experimental Botany, Sokolovská 6, Olomouc, Czech Republic.

出版信息

Nat Protoc. 2007;2(9):2233-44. doi: 10.1038/nprot.2007.310.

Abstract

Flow cytometry (FCM) using DNA-selective fluorochromes is now the prevailing method for the measurement of nuclear DNA content in plants. Ease of sample preparation and high sample throughput make it generally better suited than other methods such as Feulgen densitometry to estimate genome size, level of generative polyploidy, nuclear replication state and endopolyploidy (polysomaty). Here we present four protocols for sample preparation (suspensions of intact cell nuclei) and describe the analysis of nuclear DNA amounts using FCM. We consider the chemicals and equipment necessary, the measurement process, data analysis, and describe the most frequent problems encountered with plant material such as the interference of secondary metabolites. The purpose and requirement of internal and external standardization are discussed. The importance of using a correct terminology for DNA amounts and genome size is underlined, and its basic principles are explained.

摘要

使用DNA选择性荧光染料的流式细胞术(FCM)现已成为测量植物核DNA含量的主流方法。与其他方法(如孚尔根密度测定法)相比,样本制备简便且样本通量高,这使得它通常更适合用于估计基因组大小、生殖多倍体水平、核复制状态和内多倍体(多体性)。在此,我们介绍四种样本制备方案(完整细胞核悬液),并描述使用FCM分析核DNA含量的方法。我们考虑了所需的化学试剂和设备、测量过程、数据分析,并描述了植物材料中最常见的问题,如次生代谢物的干扰。讨论了内部和外部标准化的目的和要求。强调了使用正确的DNA含量和基因组大小术语的重要性,并解释了其基本原理。

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