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Systematic sequencing of cDNA clones using the transposon Tn5

机译:使用转座子Tn5对cDNA克隆进行系统测序

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摘要

In parallel with the production of genomic sequence data, attention is being focused on the generation of comprehensive cDNA-sequence resources. Such efforts are increasingly emphasizing the production of high-accuracy sequence corresponding to the entire insert of cDNA clones, especially those presumed to reflect the full-length mRNA. The complete sequencing of cDNA clones on a large scale presents unique challenges because of the generally small, yet heterogeneous, sizes of the cloned inserts. We have developed a strategy for high-throughput sequencing of cDNA clones using the transposon Tn5. This approach has been tailored for implementation within an existing large-scale ‘shotgun-style’ sequencing program, although it could be readily adapted for use in virtually any sequencing environment. In addition, we have developed a modified version of our strategy that can be applied to cDNA clones with large cloning vectors, thereby overcoming a potential limitation of transposon-based approaches. Here we describe the details of our cDNA-sequencing pipeline, including a summary of the experience in sequencing more than 4200 cDNA clones to produce more than 8 million base pairs of high-accuracy cDNA sequence. These data provide both convincing evidence that the insertion of Tn5 into cDNA clones is sufficiently random for its effective use in large-scale cDNA sequencing as well as interesting insight about the sequence context preferred for insertion by Tn5.
机译:在产生基因组序列数据的同时,人们将注意力集中在产生全面的cDNA序列资源上。这样的努力越来越强调与cDNA克隆的整个插入片段相对应的高精度序列的产生,特别是那些推测可反映全长mRNA的序列。 cDNA克隆的大规模完整测序提出了独特的挑战,因为克隆的插入片段通常很小,但异质。我们已经开发了使用转座子Tn5对cDNA克隆进行高通量测序的策略。尽管可以很容易地将其适应于几乎任何测序环境,但该方法是为在现有大型“ shot弹枪式”测序程序中实施而量身定制的。此外,我们已经开发出策略的修改版本,可以将其应用于具有大型克隆载体的cDNA克隆,从而克服了基于转座子方法的潜在局限性。在这里,我们描述了cDNA测序流程的细节,包括对4200多个cDNA克隆进行测序以产生800万个以上的高精度cDNA序列碱基的经验总结。这些数据提供了令人信服的证据,表明将Tn5插入cDNA克隆具有足够的随机性,可以有效地在大规模cDNA测序中使用,也提供了有关Tn5优先插入的序列背景的有趣见识。

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