Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, KS.
Biotechniques. 2013 Nov;55(5):269-72. doi: 10.2144/000114102.
A large number of methods are available to deplete ribosomal RNA reads from high-throughput RNA sequencing experiments. Such methods are critical for sequencing Drosophila small RNAs between 20 and 30 nucleotides because size selection is not typically sufficient to exclude the highly abundant class of 30 nucleotide 2S rRNA. Here we demonstrate that pre-annealing terminator oligos complimentary to Drosophila 2S rRNA prior to 5' adapter ligation and reverse transcription efficiently depletes 2S rRNA sequences from the sequencing reaction in a simple and inexpensive way. This depletion is highly specific and is achieved with minimal perturbation of miRNA and piRNA profiles.
有大量方法可用于从高通量 RNA 测序实验中去除核糖体 RNA 读数。对于测序长度在 20 到 30 个核苷酸之间的果蝇小 RNA 而言,这类方法至关重要,因为大小选择通常不足以排除高度丰富的 30 个核苷酸 2S rRNA 这一类。在这里,我们证明了在 5' 接头连接和反转录之前,将与果蝇 2S rRNA 互补的终止子寡核苷酸预退火,以简单且廉价的方式从测序反应中有效地去除 2S rRNA 序列。这种去除是高度特异性的,并且对 miRNA 和 piRNA 谱的干扰最小。