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酵母中 20nm 银纳米粒子的转录组图谱。

Transcriptome profile with 20 nm silver nanoparticles in yeast.

机构信息

Department of Biology, Missouri State University, 901 S National, Springfield, MO 65807, USA.

Kickapoo High School, 3710 S. Jefferson Ave, Springfield, MO 65807, USA.

出版信息

FEMS Yeast Res. 2019 Mar 1;19(2). doi: 10.1093/femsyr/foz003.

Abstract

Engineered nanomaterials are commercially used in everyday products including zinc sunscreens and water-resistant fabrics and surfaces. Therefore, understanding the effects of engineered nanomaterials on the environment is crucial for the responsible use of these technologies. We investigated the effects of 20 nm spherical citrate-coated silver nanoparticles (AgNPs) on the budding yeast Saccharomyces cerevisiae. Our growth assay showed that AgNPs have an inhibitory effect on yeast growth with concentrations above 5 μg/mL. Hundreds of genes in AgNP-treated cells were differentially expressed according to our transcriptome analysis based on RNAseq, including genes implicated in rRNA processing, ribosome biogenesis, cell wall formation, cell membrane integrity and mitochondrial functions. In particular, genes whose functions are associated with processing of small and large subunits of ribosomes were upregulated, while genes for cell wall/plasma membrane/mitochondrial integrity were downregulated. Consistently, our cell wall stability assay confirmed that cells with AgNPs are more susceptible to cell wall damage than non-treated cells. Levels of four significantly altered genes with AgNPs, including FAF1, SDA1, TIR1 and DAN1, were validated by reproducible results with RT-qPCR assays. Our transcriptome profile leads us to conclude that the exposure of cells to sublethal amounts of AgNPs affects many cellular processes negatively.

摘要

工程纳米材料在包括锌防晒霜和防水织物和表面在内的日常产品中得到了商业应用。因此,了解工程纳米材料对环境的影响对于这些技术的负责任使用至关重要。我们研究了 20nm 球形柠檬酸盐涂层的银纳米粒子(AgNPs)对 budding 酵母 Saccharomyces cerevisiae 的影响。我们的生长测定表明,AgNPs 在浓度高于 5μg/ml 时对酵母生长具有抑制作用。根据我们基于 RNAseq 的转录组分析,AgNP 处理细胞中的数百个基因表达水平存在差异,包括与 rRNA 加工、核糖体生物发生、细胞壁形成、细胞膜完整性和线粒体功能相关的基因。特别是与核糖体小亚基和大亚基加工相关的功能基因上调,而与细胞壁/质膜/线粒体完整性相关的基因下调。同样,我们的细胞壁稳定性测定证实,含有 AgNPs 的细胞比未经处理的细胞更容易受到细胞壁损伤。用 RT-qPCR 检测验证了四个基因(FAF1、SDA1、TIR1 和 DAN1)在 AgNPs 处理下的表达水平发生了显著变化。我们的转录组图谱使我们得出结论,细胞暴露于亚致死剂量的 AgNPs 会对许多细胞过程产生负面影响。

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