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Meta-analysis of small RNA-sequencing errors reveals ubiquitous post-transcriptional RNA modifications

机译:小RNA测序错误的荟萃分析揭示了转录后RNA的普遍修饰

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Recent advances in DNA-sequencing technology have made it possible to obtain large datasets of small RNA sequences. Here we demonstrate that not all non-perfectly matched small RNA sequences are simple technological sequencing errors, but many hold valuable biological information. Analysis of three small RNA datasets originating from Oryza sativa and Arabidopsis thaliana small RNA-sequencing projects demonstrates that many single nucleotide substitution errors overlap when aligning homologous non-identical small RNA sequences. Investigating the sites and identities of substitution errors reveal that many potentially originate as a result of post-transcriptional modifications or RNA editing. Modifications include N1-methyl modified purine nucleotides in tRNA, potential deamination or base substitutions in micro RNAs, 3' micro RNA uridine extensions and 5' micro RNA deletions. Additionally, further analysis of large sequencing datasets reveal that the combined effects of 5' deletions and 3' uridine extensions can alter the specificity by which micro RNAs associate with different Argonaute proteins. Hence, we demonstrate that not all sequencing errors in small RNA datasets are technical artifacts, but that these actually often reveal valuable biological insights to the sites of post-transcriptional RNA modifications.
机译:DNA测序技术的最新进展使得获得小RNA序列的大型数据集成为可能。在这里,我们证明并非所有非完美匹配的小RNA序列都是简单的技术测序错误,但是许多保留有价值的生物学信息。对源自稻和拟南芥小RNA测序项目的三个小RNA数据集的分析表明,在排列同源的不同小RNA序列时,许多单核苷酸取代错误会重叠。调查取代错误的位点和身份后发现,许多错误可能是由于转录后修饰或RNA编辑引起的。修饰包括tRNA中的N1-甲基修饰的嘌呤核苷酸,微小RNA中的潜在脱氨基或碱基取代,3'微小RNA尿苷延伸和5'微小RNA缺失。此外,对大型测序数据集的进一步分析表明,5'缺失和3'尿苷延伸的组合效应可以改变微RNA与不同Argonaute蛋白结合的特异性。因此,我们证明了小RNA数据集中的并非所有测序错误都是技术伪像,但实际上,这些错误通常揭示了对转录后RNA修饰位点的宝贵生物学见解。

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