Myakishev Max, Polesskaya Oksana, Kulichkova Valentina, Baranova Ancha, Gause Larissa, Konstantinova Irina
Department of Dermatology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Cell Stress Chaperones. 2008 Spring;13(1):111-6. doi: 10.1007/s12192-008-0010-z. Epub 2008 Feb 13.
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.
含有转座元件的RNA的细胞水平会因各种应激而增加。转座子的聚合酶III(Pol III)依赖性转录本不同于通过通读Pol II依赖性转录产生的含转座子的RNA。到目前为止,Pol III转录本是通过引物延伸然后进行耗时的凝胶电泳来检测的。在本文中,我们描述了一种更灵敏的基于PCR的方法,用于选择性检测Pol III转录的RNA。该方法基于Pol II和Pol III依赖性转录本5'端序列的差异。我们采用这种方法对啮齿动物细胞中转座子B1的Pol III转录本进行定量,发现其水平受紫外线照射的影响。因此,我们得出结论,细胞RNA中Pol III转录部分的丰度可作为应激反应的标志物,并且可以通过所述方法方便地进行定量。