Literature DB >> 31467221

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

Kaihang Wang1, Daniel de la Torre1, Wesley E Robertson1, Jason W Chin2.   

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.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2019        PMID: 31467221      PMCID: PMC7056355          DOI: 10.1126/science.aay0737

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  27 in total

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6.  Total synthesis of Escherichia coli with a recoded genome.

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Journal:  Microorganisms       Date:  2021-04-15

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6.  Single strain control of microbial consortia.

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7.  Twice exploration of tRNA +1 frameshifting in an elongation cycle of protein synthesis.

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9.  Enzymatic Supercoiling of Bacterial Chromosomes Facilitates Genome Manipulation.

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  9 in total

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