发布: 2014年04月05日第4卷第7期 DOI: 10.21769/BioProtoc.1094 浏览次数: 12576
评审: Masahiro MoritaRu ZhangAnonymous reviewer(s)
Abstract
Somatic homologous recombination (SHR) is a major pathway of DNA double-strand break (DSB) repair, in which intact homologous regions are used as a template for the removal of lesions. Its frequency in plants is generally low, as most DSB are removed by non-homologous mechanisms in higher eukaryotes. Nevertheless, SHR frequency has been shown to increase in response to various chemical and physical agents that cause DNA damage and/or alter genome stability (reviewed in March-Díaz and Reyes, 2009). We monitor the frequency of SHR in transgenic Arabidopsis seedlings containing recombination substrates with two truncated but overlapping parts of the β-glucuronidase (GUS) reporter gene (Orel et al., 2003; Schuermann et al., 2005). Upon an SHR event, a functional version of the transgene can be restored (Figure 1A). A histochemical assay applicable to whole plantlets allows the visualization of cells in which the reporter is restored, as the encoded enzyme converts a colorless substrate into a blue compound. This type of reporter has been extensively used to identify gene products required for regulating SHR levels in plants. We analyze plants stimulated for SHR by treatments with DNA damaging agents (bleocin, mitomycin C and UV-C) and compare them to non-treated plants.
Keywords: Homologous recombination (同源重组)Materials and Reagents
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文章信息
版权信息
© 2014 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Rosa, M. and Scheid, O. M. (2014). Measuring Homologous Recombination Frequency in Arabidopsis Seedlings. Bio-protocol 4(7): e1094. DOI: 10.21769/BioProtoc.1094.
分类
植物科学 > 植物生理学 > 组织分析
植物科学 > 植物分子生物学 > DNA
分子生物学 > DNA > DNA 重组
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