马拉松 RT 模板切换反应的特征和实施,以扩展 RNA-Seq 的功能。

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2024-10-16 DOI:10.1261/rna.080032.124
Li-Tao Guo, Anastasiya Grinko, Sara Olson, Alexander M Leipold, Brenton Graveley, Antoine-Emmanuel Saliba, Anna Marie Pyle
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引用次数: 0

摘要

端到端 RNA 测序方法无需对文库进行繁琐的操作就能捕获 5'- 序列内容,这引起了人们极大的兴趣,尤其是在分析长 RNA 时。虽然模板切换方法是为分布式短读RT(如SMART-Seq方法中使用的MMLV RT酶)的RNA测序而开发的,但它们还没有适应于利用超进程RT的能力,如来自第二组自剪接内含子的RT。为了促进这一转变,我们剖析了指导 RT 酶(在本例中是由一种被称为 MarathonRT 的特性良好的酶进行的)多步骤模板切换反应的酶特异性和效率的各个过程。值得注意的是,这是首次针对任何 RT 进行此类研究。首先,我们表征并优化了 RT 酶延伸至 RNA 5'-terminus 后发生的酶促非模板加成(NTA)反应,并确定了 NTA 反应的核苷酸特异性。然后,我们评估了专用模板切换寡核苷酸的结合特异性,优化了它们的序列和化学性质,以指导高效的模板切换反应。在对这些单独步骤进行剖析和优化后,我们将它们整合到一个程序中,利用马拉松 RT 酶,使用表征良好的 RNA 参考集进行 RNA 测序。由此产生的读数在转录本浓度上跨越了六个对数的范围,并在长度和组成上准确地代表了输入 RNA 的特性。我们还从人类总 RNA 和多聚(A)富集 RNA 开始进行了 RNA-seq,用短线程和长线程测序证明,MarathonRT 提高了传统 RT 发现未知 RNA 分子的能力。总之,通过对RT酶进行机理酶学研究,并利用它们对RNA-seq技术进行改造,我们开发出了一种新的方法,可对含有长RNA转录本混合物的复杂RNA文库进行快速、准确的测序。
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Characterization and implementation of the MarathonRT template-switching reaction to expand the capabilities of RNA-seq.

End-to-end RNA-sequencing methods that capture 5'-sequence content without cumbersome library manipulations are of great interest, particularly for analysis of long RNAs. While template-switching methods have been developed for RNA sequencing by distributive short-read RTs, such as the MMLV RTs used in SMART-Seq methods, they have not been adapted to leverage the power of ultraprocessive RTs, such as those derived from group II introns. To facilitate this transition, we dissected the individual processes that guide the enzymatic specificity and efficiency of the multistep template-switching reaction carried out by RTs, in this case, by MarathonRT. Remarkably, this is the first study of its kind, for any RT. First, we characterized the nucleotide specificity of nontemplated addition (NTA) reaction that occurs when the RT extends past the RNA 5'-terminus. We then evaluated the binding specificity of specialized template-switching oligonucleotides, optimizing their sequences and chemical properties to guide efficient template-switching reaction. Having dissected and optimized these individual steps, we then unified them into a procedure for performing RNA sequencing with MarathonRT enzymes, using a well-characterized RNA reference set. The resulting reads span a six-log range in transcript concentration and accurately represent the input RNA identities in both length and composition. We also performed RNA-seq from total human RNA and poly(A)-enriched RNA, with short- and long-read sequencing demonstrating that MarathonRT enhances the discovery of unseen RNA molecules by conventional RT. Altogether, we have generated a new pipeline for rapid, accurate sequencing of complex RNA libraries containing mixtures of long RNA transcripts.

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来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
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