Lambert Marine, Guellal Sara, Ho Jeffrey, Benmoussa Abderrahim, Laffont Benoit, Bélanger Richard, Provost Patrick
CHU de Québec-Université Laval Research Center/CHUL Pavilion, 2705 Blvd. Laurier, Quebec City, QC G1V 4G2, Canada.
Department of Microbiology, Infectious Diseases and Immunology, Faculty of Medicine, Université Laval, Quebec City, QC G1V 0A6, Canada.
Noncoding RNA. 2022 May 19;8(3):34. doi: 10.3390/ncrna8030034.
Small RNA sequencing (sRNA-Seq) approaches unveiled sequences derived from longer non-coding RNAs, such as transfer RNA (tRNA) and ribosomal RNA (rRNA) fragments, known as tRFs and rRFs, respectively. However, rRNAs and RNAs shorter than 16 nt are often depleted from library preparations/sequencing analyses, although they may be functional. Here, we sought to obtain a complete repertoire of small RNAs by sequencing the total RNA from 11 samples of 6 different eukaryotic organisms, from yeasts to human, in an extended 8- to 30-nt window of RNA length. The 8- to 15-nt window essentially contained fragments of longer non-coding RNAs, such as microRNAs, PIWI-associated RNAs (piRNAs), small nucleolar RNAs (snoRNAs), tRNAs and rRNAs. Notably, unusually short RNAs < 16 nt were more abundant than those >16 nt in bilaterian organisms. A new RT-qPCR method confirmed that two unusually short rRFs of 12 and 13 nt were more overly abundant (~3-log difference) than two microRNAs. We propose to not deplete rRNA and to reduce the lower threshold of RNA length to include unusually short RNAs in sRNA-Seq analyses and datasets, as their abundance and diversity support their potential role and importance as biomarkers of disease and/or mediators of cellular function.
小RNA测序(sRNA-Seq)方法揭示了源自较长非编码RNA的序列,例如分别称为tRFs和rRFs的转运RNA(tRNA)和核糖体RNA(rRNA)片段。然而,rRNA和短于16个核苷酸的RNA在文库制备/测序分析中常常被去除,尽管它们可能具有功能。在这里,我们试图通过对来自6种不同真核生物(从酵母到人类)的11个样本的总RNA进行测序,在8至30个核苷酸的扩展RNA长度窗口中获得小RNA的完整文库。8至15个核苷酸的窗口主要包含较长非编码RNA的片段,如微小RNA、PIWI相互作用RNA(piRNA)、小核仁RNA(snoRNA)、tRNA和rRNA。值得注意的是,在两侧对称生物中,长度小于16个核苷酸的异常短RNA比长度大于16个核苷酸的RNA更为丰富。一种新的RT-qPCR方法证实,两个12和13个核苷酸的异常短rRF比两个微小RNA的丰度更高(相差约3个对数)。我们建议在sRNA-Seq分析和数据集中不去除rRNA,并降低RNA长度的下限以纳入异常短的RNA,因为它们的丰度和多样性支持它们作为疾病生物标志物和/或细胞功能介质的潜在作用和重要性。