分析和控制非模板 DNA 聚合酶活性,引导合成千碱基级 DNA 序列

Simeon D. Castle, Adrian Woolfson, Gregory Linshiz, Blake T. Riley, Ifor D.W. Samuel, Philipp Holliger, Lauren Oldfield, Andrew Hessel, Thomas E. Gorochowski
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引用次数: 0

摘要

DNA 聚合酶是一种复杂的分子机器,能够利用模板驱动过程复制遗传物质。虽然这些酶的复制功能已得到公认,但它们进行无模板 DNA 合成的能力却没有得到很好的描述。在这里,我们探讨了 DNA 聚合酶在没有模板的情况下合成 DNA 片段的能力。我们使用长线程纳米孔测序和实时聚合酶链式反应(real-time PCR)技术,观察了不同温度和缓冲液成分下由多种天然和工程 DNA 聚合酶合成的 DNA 产物池。我们详细介绍了所生成 DNA 片段的特征、所选序列图案的富集情况,并证明合成 DNA 的序列组成可能会因环境条件的改变而改变。这项工作提供了一个广泛的数据集,以更好地辨别非模板 DNA 聚合酶的活动过程,并可能支持将其重新用作千碱基级甚至更高的 DNA 序列引导合成技术。
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Analysis and control of untemplated DNA polymerase activity for guided synthesis of kilobase-scale DNA sequences
DNA polymerases are complex molecular machines able to replicate genetic material using a template-driven process. While the copying function of these enzymes is well established, their ability to perform untemplated DNA synthesis is less well characterized. Here, we explore the ability of DNA polymerases to synthesize DNA fragments in the absence of template. We use long-read nanopore sequencing and real-time PCR to observe the synthesis of pools of DNA products derived from a diverse set of natural and engineered DNA polymerases across varying temperatures and buffer compositions. We detail the features of the DNA fragments generated, enrichment of select sequence motifs, and demonstrate that the sequence composition of the synthesized DNA may be altered by modifying environmental conditions. This work provides an extensive data set to better discern the process of untemplated DNA polymerase activity and may support its potential repurposing as a technology for the guided synthesis of DNA sequences on the kilobase-scale and beyond.
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