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PCR-based detection of Pol III-transcribed transposons and its application to the rodent model of ultraviolet response

机译:基于PCR的Pol III转录转座子的检测及其在啮齿类动物紫外线反应中的应用

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摘要

Cellular levels of RNAs containing transposable elements increase in response to various stresses. Polymerase III (Pol III)-dependent transcripts of transposons are different from transposon-containing RNAs generated by read-through Pol II-dependent transcription. Until now, Pol III transcripts were detected by primer extension followed by time-consuming gel electrophoresis. In this paper, we describe a more sensitive PCR-based method for the selective detection of Pol III-transcribed RNAs. The method is based on the difference in sequences at the 5′ ends of the Pol II- and Pol III-dependent transcripts. We employed this method to quantify Pol III transcripts of transposon B1 in rodent cells and revealed that their levels are affected by UV irradiation. We therefore conclude that the abundance of the Pol III-transcribed fraction of cellular RNA may serve as marker of stress response and can be conveniently quantified by the method described.
机译:包含转座因子的RNA的细胞水平响应各种压力而增加。转座子的聚合酶III(Pol III)依赖性转录物与通读Pol II依赖性转录产生的含转座子的RNA不同。到目前为止,通过引物延伸和费时的凝胶电泳来检测Pol III转录本。在本文中,我们描述了一种基于PCR的更加敏感的方法,用于选择性检测Pol III转录的RNA。该方法是基于依赖于Pol II和Pol III的转录本5'端的序列差异。我们采用这种方法来量化转基因动物B1在啮齿动物细胞中的Pol III转录本,并揭示它们的水平受紫外线辐射的影响。因此,我们得出结论,细胞RNA的Pol III转录级分的丰度可以作为应激反应的标志,可以通过所述方法方便地进行定量。

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