DNA synthesis technologies to close the gene writing gap

合成生物学 DNA测序 DNA DNA合成 计算生物学 计算机科学 纳米技术 生物 遗传学 材料科学
作者
Alex Hoose,Richard Vellacott,Marko Storch,Paul S. Freemont,Maxim G. Ryadnov
出处
期刊:Nature Reviews Chemistry [Nature Portfolio]
卷期号:7 (3): 144-161 被引量:264
标识
DOI:10.1038/s41570-022-00456-9
摘要

Synthetic DNA is of increasing demand across many sectors of research and commercial activities. Engineering biology, therapy, data storage and nanotechnology are set for rapid developments if DNA can be provided at scale and low cost. Stimulated by successes in next generation sequencing and gene editing technologies, DNA synthesis is already a burgeoning industry. However, the synthesis of >200 bp sequences remains unaffordable. To overcome these limitations and start writing DNA as effectively as it is read, alternative technologies have been developed including molecular assembly and cloning methods, template-independent enzymatic synthesis, microarray and rolling circle amplification techniques. Here, we review the progress in developing and commercializing these technologies, which are exemplified by innovations from leading companies. We discuss pros and cons of each technology, the need for oversight and regulatory policies for DNA synthesis as a whole and give an overview of DNA synthesis business models. There is increasing demand for synthetic DNA. However, our ability to make, or write, DNA lags behind our ability to sequence, or read, it. This Review discusses commercialized DNA synthesis technologies in the pursuit of closing the DNA writing gap.
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