首页> 外文期刊>Nucleic Acids Research >Promoter-trapping in Saccharomyces cerevisiae by radiation-assisted fragment insertion - art. no. e136
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Promoter-trapping in Saccharomyces cerevisiae by radiation-assisted fragment insertion - art. no. e136

机译:通过辐射辅助片段插入在酿酒酵母中捕获启动子-艺术。没有。 e136

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摘要

Non-homologous insertion (NHI) of DNA fragments into genomic DNA is a method widely used in insertional mutagenesis screens. In the yeast Saccharomyces cerevisiae, the efficiency of NHI is very low. Here we report that its efficiency can be increased by gamma-irradiation of recipient cells at the time of transformation. Radiation-assisted NHI depends on YKU70, but its efficiency is not improved by inactivation of RAD5 or RAD52. In a pilot study, we generated 102 transformant clones expressing a lacZ reporter gene under standard conditions (30degreesC, rich medium). The site of insertion was determined in a subset of eight clones in which lacZ expression was altered by UV-irradiation. A comparison with published data revealed that three of the eight genes identified in our screen have not been targeted by large-scale transposon-based insertion screens. This suggests that radiation-assisted NHI offers a more homogeneous coverage of the genome than methods relying on transposons or retroviral elements.
机译:DNA片段在基因组DNA中的非同源插入(NHI)是一种广泛用于插入诱变筛选的方法。在酵母酿酒酵母中,NHI的效率非常低。在这里,我们报道其转化时的受体细胞可以通过γ射线辐照来提高其效率。辐射辅助NHI依赖于YKU70,但是通过灭活RAD5或RAD52并不能提高其效率。在一项初步研究中,我们在标准条件(30℃,富培养基)下产生了表达lacZ报告基因的102个转化子克隆。在八个克隆的子集中确定插入位点,其中通过紫外线照射改变了lacZ表达。与已发表数据的比较表明,在我们的筛选中鉴定出的八个基因中的三个尚未被大规模的基于转座子的插入筛选所针对。这表明,与依赖转座子或逆转录病毒元件的方法相比,辐射辅助NHI提供了更均匀的基因组覆盖范围。

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