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Mutually Orthogonal DNA Replication Systems In Vivo

机译:体内相互正交的DNA复制系统

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摘要

The yeast cytoplasmically localized pGKL1/TP-DNAP1 plasmid/DNA polymerase pair forms an orthogonal DNA replication system whose mutation rate can be drastically increased without influencing genomic replication, thereby supporting in vivo continuous evolution. Here, we report that the pGKL2/TP-DNAP2 plasmid/DNA polymerase pair forms a second orthogonal replication system. We show that custom genes can be encoded and expressed from pGKL2, that error-prone TP-DNAP2s can be engineered, and that pGKL2 replication by TP-DNAP2 is both orthogonal to genomic replication in Saccharomyces cerevisiae and mutually orthogonal with pGKL1 replication by TP-DNAP1. This demonstration of two mutually orthogonal DNA replication systems with tunable error rates and properties should enable new applications in cell-based continuous evolution, genetic recording, and synthetic biology at large.
机译:酵母细胞质局部化的PGK1 / TP-DNAP1质粒/ DNA聚合酶对形成正交DNA复制系统,其突变率可以大大增加而不影响基因组复制,从而支撑体内连续演化。 在此,我们报告称PGK12 / TP-DNAP2质粒/ DNA聚合酶对形成第二正交复制系统。 我们表明,可以从PGK12编码和表达自定义基因,可以设计出易于易于的TP-DNAP2S,并且TP-DNAP2的PGKL2复制均正交与Saccharomyces酿酒酵母中的基因组复制,并通过TP与PGKL1复制相互正交 dnap1。 这种具有可调误差速率和性能的两个相互正交的DNA复制系统的演示应使新应用在基于单元的连续演化,遗传记录和大的合成生物中。

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