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利用根癌农杆菌的T-DNA在酵母中进行插入诱变。

Insertional mutagenesis in yeasts using T-DNA from Agrobacterium tumefaciens.

作者信息

Bundock Paul, van Attikum Haico, den Dulk-Ras Amke, Hooykaas Paul J J

机构信息

Institute for Molecular Plant Sciences, Wassenaarseweg 64, 2333 AL Leiden, The Netherlands.

出版信息

Yeast. 2002 Apr;19(6):529-36. doi: 10.1002/yea.858.

Abstract

Insertional mutagenesis is a powerful tool for the isolation of novel mutations. The gene delivery system of the bacterium Agrobacterium tumefaciens, which mediates transfer not only to plants but also to yeasts and fungi, could be exploited to generate collections of yeasts containing insertional mutations if there were no bias towards particular integration sites, as is the case in plants. To test this, we have analysed a small collection of Saccharomyces cerevisiae strains with T-DNA copies integrated in the S. cerevisiae genome. The position of 54 of these T-DNAs was determined. The T-DNA showed no clear preference for certain DNA sequences or genomic regions. We have isolated insertions in the coding regions of the genes YGR125w, YDR250c, YGR141w, YGR045c, YPL017c, YGR040w, YDL052c, YJL148w, YCL033c, YFL061w, YJR033c, YDR175c and YLR309c confirming that these genes are non-essential for S. cerevisiae haploid growth on minimal medium. Given the advantages of T-DNA, we propose its use as an ideal mobile DNA element for insertional mutagenesis in yeasts.

摘要

插入诱变是分离新突变的有力工具。根癌土壤杆菌的基因传递系统不仅能介导基因转移至植物,还能转移至酵母和真菌。如果不存在像在植物中那样对特定整合位点的偏好,就可以利用该系统来生成含有插入突变的酵母文库。为了验证这一点,我们分析了一小批在酿酒酵母基因组中整合有T-DNA拷贝的酿酒酵母菌株。确定了其中54个T-DNA的位置。T-DNA对某些DNA序列或基因组区域没有明显的偏好。我们在基因YGR125w、YDR250c、YGR141w、YGR045c、YPL017c、YGR040w、YDL052c、YJL148w、YCL033c、YFL061w、YJR033c、YDR175c和YLR309c的编码区分离到了插入突变,证实这些基因对于酿酒酵母在基本培养基上的单倍体生长并非必需。鉴于T-DNA的优势,我们建议将其用作酵母插入诱变的理想移动DNA元件。

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