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请勿打扰:通过一种新型的DNA-组蛋白相互作用检测方法揭示超活核酸探针破坏染色质结构

Please do not disturb: destruction of chromatin structure by supravital nucleic acid probes revealed by a novel assay of DNA-histone interaction.

作者信息

Wlodkowic Donald, Darzynkiewicz Zbigniew

机构信息

Department of Biological Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, United Kingdom.

出版信息

Cytometry A. 2008 Oct;73(10):877-9. doi: 10.1002/cyto.a.20622.

Abstract

The biomarkers designed to be used supravitally are expected to have minimal effect on structure and function of the cell. Unfortunately nearly all fluorochromes developed to probe live cells interact in undesired way with cellular constituents and affect functional pathways. Herein we comment on potential applications of diverse DNA binding probes in view of the recent article by Wojcik & Dobrucki on DRAQ 5 and SYTO 17. The approach used by these authors to assess DNA-histone interactions using the cells having histones tagged with fluorescent proteins offers a valuable tool to study mechanism of action of antitumor drugs targeting DNA. While the effect of many intercalating drugs may be similar to that of DRAQ5, it may be of particular interest to observe the effects induced by intra-strand and inter-strand DNA crosslinking drugs, alkylating agents, histone deacetylase inhibitors or even anti-metabolites. The cells having histones tagged with fluorescent proteins thus may serve as biomarkers to probe mechanism of action of drugs targeting DNA or affecting chromatin structure. In fact, because such gross chromatin changes as revealed by dissociation and segregation of histones from DNA are most likely incompatible with long-term cell survival, the methodology may be applied for rapid screening of investigational antitumor agents.

摘要

设计用于活体细胞染色的生物标志物应尽量减少对细胞结构和功能的影响。遗憾的是,几乎所有用于探测活细胞的荧光染料都会与细胞成分发生非预期的相互作用,进而影响细胞的功能通路。鉴于Wojcik和Dobrucki最近发表的关于DRAQ 5和SYTO 17的文章,本文将对多种DNA结合探针的潜在应用进行评论。这些作者使用带有荧光蛋白标记组蛋白的细胞来评估DNA - 组蛋白相互作用的方法,为研究靶向DNA的抗肿瘤药物的作用机制提供了一个有价值的工具。虽然许多嵌入剂药物的作用可能与DRAQ5类似,但观察链内和链间DNA交联药物、烷基化剂、组蛋白脱乙酰酶抑制剂甚至抗代谢物所诱导的效应可能会特别有意义。因此,带有荧光蛋白标记组蛋白的细胞可以作为生物标志物,用于探测靶向DNA或影响染色质结构的药物的作用机制。事实上,由于组蛋白从DNA上解离和分离所揭示的这种明显的染色质变化很可能与细胞的长期存活不相容,该方法可用于快速筛选研究性抗肿瘤药物。

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