Extra perspectives of 5-ethynyl-2'-deoxyuridine click reaction with fluorochrome azides to study cell cycle and deoxyribonucleoside metabolism

被引:4
|
作者
Nosov, A. V. [1 ]
Fomenkov, A. A. [1 ]
Mamaeva, A. S. [1 ]
Solovchenko, A. E. [1 ,2 ]
Novikova, G. V. [1 ]
机构
[1] Russian Acad Sci, Timiryazev Inst Plant Physiol, Moscow 127276, Russia
[2] Moscow MV Lomonosov State Univ, Fac Biol, Moscow, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
Arabidopsis thaliana; Chlamydomonas reinhardtii; Synechocystis; Vigna radiata; cell cycle; cell culture; nucleotides; S-period; protoplasts; flow cytometry; thymidine kinase; fluorescence microscopy; THYMIDINE KINASE; DNA; PHOSPHORYLATION; REPLICATION; TRANSPORT; GROWTH;
D O I
10.1134/S1021443714060144
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Beginning with the pioneering work of Salic and Mitchison (2008), the application of thymidine analogue 5-ethynyl-2'-deoxyuridine (EdU) for the detection of cells replicating DNA is actively expanding. Being incorporated into DNA, this nucleoside after click reaction of azide-alkyne cycloaddition with azides of fluorochromes can be easily detected by fluorescence. Recently, protocols of EdU application in combination with click reaction adapted for plant cells appeared, and they are help for a monitoring S-period of the cell cycle in the root meristems and in vitro cultured cells with the help of a microscope and flow cytometer. In this work, we focused some details of developed methods and their modifications and also recommended new protocols. In particular, we suggested combining EdU incorporation into the cells replicating DNA with subsequent isolation of protoplasts from them and their preparation for the microscopic analysis and flow cytometry. In addition, the method of determination of EdU phosphorylation dynamics in the cells in vivo is suggested.
引用
收藏
页码:899 / 909
页数:11
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