CasHRA (Cas9-facilitated Homologous Recombination Assembly) method of constructing megabase-sized DNA

• Published in: Nucleic acids research Vol. 44; no. 14; p. e124
• Main Authors: Zhou, Jianting, Wu, Ronghai, Xue, Xiaoli, Qin, Zhongjun
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 19-08-2016
• Subjects: Base Pairing - genetics; CRISPR-Associated Proteins - metabolism; DNA, Bacterial - genetics; DNA, Bacterial - metabolism; DNA, Circular; Escherichia coli - genetics; Genome, Bacterial; Homologous Recombination - genetics; Methods Online; Saccharomyces cerevisiae; Synthetic Biology - methods
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkw475

Current DNA assembly methods for preparing highly purified linear subassemblies require complex and time-consuming in vitro manipulations that hinder their ability to construct megabase-sized DNAs (e.g. synthetic genomes). We have developed a new method designated 'CasHRA (Cas9-facilitated Homologous Recombination Assembly)' that directly uses large circular DNAs in a one-step in vivo assembly process. The large circular DNAs are co-introduced into Saccharomyces cerevisiae by protoplast fusion, and they are cleaved by RNA-guided Cas9 nuclease to release the linear DNA segments for subsequent assembly by the endogenous homologous recombination system. The CasHRA method allows efficient assembly of multiple large DNA segments in vivo; thus, this approach should be useful in the last stage of genome construction. As a proof of concept, we combined CasHRA with an upstream assembly method (Gibson procedure of genome assembly) and successfully constructed a 1.03 Mb MGE-syn1.0 (Minimal Genome of Escherichia coli) that contained 449 essential genes and 267 important growth genes. We expect that CasHRA will be widely used in megabase-sized genome constructions.