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组织胞浆菌插入诱变的 T-DNA 整合谱。

Spectrum of T-DNA integrations for insertional mutagenesis of Histoplasma capsulatum.

机构信息

Department of Microbiology, Ohio State University, Columbus, OH 43210, USA.

出版信息

Fungal Biol. 2013 Jan;117(1):41-51. doi: 10.1016/j.funbio.2012.11.004. Epub 2012 Dec 2.

Abstract

Agrobacterium-mediated transformation is being increasingly used for insertional mutagenesis of fungi. To better evaluate its effectiveness as a mutagen for the fungal pathogen Histoplasma capsulatum, we analyzed a collection of randomly selected T-DNA insertion mutants. Testing of different T-DNA element vectors engineered for transformation of fungi showed that pBHt2 provides the highest transformation efficiency and the lowest rate of vector backbone carryover. Sixty-eight individual T-DNA integrations were characterized by recovery of T-DNA ends and flanking genomic sequences. The right border (RB) end of the T-DNA is largely preserved whereas the left border (LB) end is frequently truncated. Analysis of T-DNA insertion sites confirms the lack of any integration hotspots in the Histoplasma genome. Relative to genes, T-DNA integrations show significant bias towards promoter regions at the expense of coding sequences. With consideration for potential promoter interruption and the demonstrated efficacy of intronic insertions, 61 % of mapped T-DNA insertions should impair gene expression or function. Mapping of T-DNA flanking sequences demonstrates 67 % of T-DNA integrations are integrations at a single chromosomal site and 31 % of T-DNA integrations are associated with large-scale chromosomal rearrangements. This characterization of T-DNA insertions in mutants selected without regard to phenotype supports application of Agrobacterium-mediated transformation as an insertional mutagen for genome-based screens and functional discovery of genes in Histoplasma.

摘要

农杆菌介导的转化正越来越多地被用于真菌的插入诱变。为了更好地评估其作为真菌病原体荚膜组织胞浆菌插入诱变剂的有效性,我们分析了一组随机选择的 T-DNA 插入突变体。测试了为真菌转化设计的不同 T-DNA 元件载体,结果表明 pBHt2 提供了最高的转化效率和最低的载体骨架残留率。通过回收 T-DNA 末端和侧翼基因组序列,对 68 个单独的 T-DNA 整合进行了特征分析。T-DNA 的右边界(RB)末端大部分被保留,而左边界(LB)末端经常被截断。T-DNA 插入位点的分析证实了荚膜组织胞浆菌基因组中不存在任何整合热点。相对于基因,T-DNA 整合显示出明显偏向于启动子区域的趋势,牺牲了编码序列。考虑到潜在的启动子中断和内含子插入的有效性,映射的 T-DNA 插入中 61%应该会损害基因表达或功能。T-DNA 侧翼序列的映射表明,67%的 T-DNA 整合是在单个染色体位点的整合,31%的 T-DNA 整合与大规模染色体重排有关。这种对选择不考虑表型的突变体中 T-DNA 插入的特征支持将农杆菌介导的转化作为基因组筛选和荚膜组织胞浆菌基因功能发现的插入诱变剂的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cd/3552300/f073b14e441d/nihms426593f1.jpg

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