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Published August 30, 2019 | Supplemental Material
Journal Article Open

Programmed chromosome fission and fusion enable precise large-scale genome rearrangement and assembly

Abstract

The design and creation of synthetic genomes provide a powerful approach to understanding and engineering biology. However, it is often limited by the paucity of methods for precise genome manipulation. Here, we demonstrate the programmed fission of the Escherichia coli genome into diverse pairs of synthetic chromosomes and the programmed fusion of synthetic chromosomes to generate genomes with user-defined inversions and translocations. We further combine genome fission, chromosome transplant, and chromosome fusion to assemble genomic regions from different strains into a single genome. Thus, we program the scarless assembly of new genomes with nucleotide precision, a key step in the convergent synthesis of genomes from diverse progenitors. This work provides a set of precise, rapid, large-scale (megabase) genome-engineering operations for creating diverse synthetic genomes.

Additional Information

© 2019 American Association for the Advancement of Science. This is an article distributed under the terms of the Science Journals Default License. Received 17 May 2019; accepted 2 August 2019. We thank J. Houseley and J. Ajioka for providing equipment for pulsed-field gel electrophoresis and J.E. Sale for helpful comments on the manuscript. Funding: This work was supported by the Medical Research Council (MRC), UK (MC_U105181009 and MC_UP_A024_1008), and an ERC Advanced Grant SGCR, all to J.W.C. Author contributions: K.W. designed and implemented the genome manipulation processes reported. K.W., D.d.l.T., and W.E.R. demonstrated scope. D.d.l.T. implemented the de novo assembly approach. J.W.C. defined the direction of research, supervised the project, and wrote the paper with the other authors. Competing interests: The authors declare no competing interests. Data and materials availability: The sequences for de novo genome assemblies and DNA sequencing data have been deposited in NCBI's GenBank and SRA databases, and their accession numbers are listed in table S4. All other data needed to evaluate the conclusions of the study are present in the paper or the supplementary materials.

Attached Files

Supplemental Material - Wang_aay0737_SM.pdf

Supplemental Material - aay0737_Wang_Data-Files-S1-S7.zip

Supplemental Material - aay0737_Wang_TableS1.xlsx

Supplemental Material - aay0737_Wang_TableS2.xlsx

Supplemental Material - aay0737_Wang_TableS6.xlsx

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August 19, 2023
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