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深度测序揭示了瞬时转染质粒中复杂的假转录。

Deep sequencing reveals complex spurious transcription from transiently transfected plasmids.

机构信息

Institute of Molecular Genetics AS CR, Prague, Czech Republic.

出版信息

PLoS One. 2012;7(8):e43283. doi: 10.1371/journal.pone.0043283. Epub 2012 Aug 16.

Abstract

Transient plasmid transfection is a common approach in studies in cultured mammalian cells. To examine behavior of transfected plasmids, we analyzed their transcriptional landscape by deep sequencing. We have found that the entire plasmid sequence is transcribed at different levels. Spurious transcription may have undesirable effects as some plasmids, when co-transfected, inhibited expression of luciferase reporters in a dose-dependent manner. In one case, we attributed this effect to a Kan/Neo resistance cassette, which generated a unique population of edited sense and antisense small RNAs. The unexpected complexity of expression from transiently transfected plasmids underscores the importance of appropriate experimental controls.

摘要

瞬时质粒转染是在培养的哺乳动物细胞中进行研究的常用方法。为了研究转染质粒的行为,我们通过深度测序分析了它们的转录图谱。我们发现整个质粒序列以不同的水平转录。由于一些质粒在共转染时会以剂量依赖的方式抑制荧光素酶报告基因的表达,因此这种异常转录可能会产生不良影响。在一种情况下,我们将这种效应归因于 Kan/Neo 抗性盒,该抗性盒产生了独特的编辑有义链和反义小 RNA 群体。瞬时转染质粒表达的出乎意料的复杂性突出了适当实验对照的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/3420890/2d40f277f78b/pone.0043283.g001.jpg

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