Institute of Molecular Systems Biology, Department of Biology, Eidgenössische Technische Hochschule Zürich, Zürich, Switzerland.
Nat Commun. 2021 May 24;12(1):3053. doi: 10.1038/s41467-021-23362-y.
Sequence rewriting enables low-cost genome synthesis and the design of biological systems with orthogonal genetic codes. The error-free, robust rewriting of nucleotide sequences can be achieved with a complete annotation of gene regulatory elements. Here, we compare transcription in Caulobacter crescentus to transcription from plasmid-borne segments of the synthesized genome of C. ethensis 2.0. This rewritten derivative contains an extensive amount of supposedly neutral mutations, including 123'562 synonymous codon changes. The transcriptional landscape refines 60 promoter annotations, exposes 18 termination elements and links extensive transcription throughout the synthesized genome to the unintentional introduction of sigma factor binding motifs. We reveal translational regulation for 20 CDS and uncover an essential translational regulatory element for the expression of ribosomal protein RplS. The annotation of gene regulatory elements allowed us to formulate design principles that improve design schemes for synthesized DNA, en route to a bright future of iteration-free programming of biological systems.
序列重写使低成本的基因组合成和具有正交遗传密码的生物系统设计成为可能。通过对基因调控元件进行完整注释,可以实现无错误、稳健的核苷酸序列重写。在这里,我们将新月柄杆菌中的转录与合成的 C. ethensis 2.0 基因组中质粒携带片段的转录进行了比较。这个重写的衍生物包含了大量所谓的中性突变,包括 123'562 个同义密码子变化。转录景观细化了 60 个启动子注释,暴露了 18 个终止元件,并将整个合成基因组中的广泛转录与 sigma 因子结合基序的意外引入联系起来。我们为 20 个 CDS 揭示了翻译调控,并发现了核糖体蛋白 RplS 表达所必需的翻译调控元件。基因调控元件的注释使我们能够制定设计原则,从而改进合成 DNA 的设计方案,为无迭代的生物系统编程的美好未来铺平道路。