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烟曲霉基因间“安全避难所”区域。

An intergenic "safe haven" region in Aspergillus fumigatus.

机构信息

Department of Microbiology, University of Georgia, Athens, Georgia, USA.

出版信息

Med Mycol. 2020 Nov 10;58(8):1178-1186. doi: 10.1093/mmy/myaa009.

Abstract

Aspergillus fumigatus is the most common opportunistic human fungal pathogen responsible for invasive aspergillosis. Gene manipulation is critical for the investigation of A. fumigatus biology and pathogenesis at the molecular level, and it often requires integration of the introduced DNA into the fungal genome. Here we have searched and identified two potential "safe haven" regions, SH1 and SH2, based on A. fumigatus genome annotation and transcriptome data. When a DNA fragment carrying a fluorescent protein gene mNeonGreen (mNG) and a drug selection marker was inserted into SH1 or SH2, the expression of mNeonGreen was easily detected, indicating that SH1 and SH2 are not surpressive genetic regions. We found that insertion of this DNA fragment into SH1 did not cause any significant changes in the expression of neighboring genes. Insertion of this DNA into either SH1 or SH2 did not significantly alter any of the phenotypes that we analyzed comparing to the wild type control. By comparison, transformants with random ectopic integration of the same DNA fragment showed a wider range of variation in mNeonGreen expression and in virulence in an insect infection model. Having identified predetermined "safe-haven" regions in A. fumigatus could therefore help reduce experimental variations and increase reproducibility, as it has been for the C. neoformans field.

摘要

烟曲霉是最常见的机会性人类真菌病原体,可导致侵袭性曲霉病。基因操作对于在分子水平上研究烟曲霉的生物学和发病机制至关重要,并且通常需要将引入的 DNA 整合到真菌基因组中。在这里,我们根据烟曲霉基因组注释和转录组数据搜索并鉴定了两个潜在的“安全避难所”区域 SH1 和 SH2。当携带荧光蛋白基因 mNeonGreen (mNG) 和药物选择标记的 DNA 片段插入 SH1 或 SH2 时,很容易检测到 mNeonGreen 的表达,表明 SH1 和 SH2 不是抑制性遗传区域。我们发现,将此 DNA 片段插入 SH1 不会导致邻近基因表达发生任何显著变化。与野生型对照相比,将此 DNA 片段插入 SH1 或 SH2 中不会显著改变我们分析的任何表型。相比之下,具有相同 DNA 片段随机异位整合的转化体在昆虫感染模型中的 mNeonGreen 表达和毒力方面表现出更广泛的变化范围。因此,在烟曲霉中鉴定预定的“安全避难所”区域可以帮助减少实验变异性并提高可重复性,就像新型隐球菌领域一样。

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