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  Large-scale genomic rearrangements boost SCRaMbLE in Saccharomyces cerevisiae

Cheng, L., Zhao, S., Li, T., Hou, S., Luo, Z., Xu, J., et al. (2024). Large-scale genomic rearrangements boost SCRaMbLE in Saccharomyces cerevisiae. Nature Communications, 15(1): 770. doi:10.1038/s41467-023-44511-5.

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https://doi.org/10.1038/s41467-023-44511-5 (Publisher version)
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 Creators:
Cheng, Li1, Author
Zhao, Shijun1, Author
Li, Tianyi1, Author
Hou, Sha1, Author
Luo, Zhouqing1, Author
Xu, Jinsheng1, Author
Yu, Wenfei1, Author
Jiang, Shuangying1, Author
Monti, Marco1, Author
Schindler, Daniel2, Author                 
Zhang, Weimin1, Author
Hou, Chunhui1, Author
Ma, Yingxin1, Author
Cai, Yizhi1, Author
Boeke, Jef D.1, Author
Dai, Junbiao1, Author
Affiliations:
1external, ou_persistent22              
2Manchester Institute of Biotechnology, University of Manchester, UK, ou_persistent22              

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 Abstract: Synthetic Chromosome Rearrangement and Modification by LoxP-mediated Evolution (SCRaMbLE) is a promising tool to study genomic rearrangements. However, the potential of SCRaMbLE to study genomic rearrangements is currently hindered, because a strain containing all 16 synthetic chromosomes is not yet available. Here, we construct SparLox83R, a yeast strain containing 83 loxPsym sites distributed across all 16 chromosomes. SCRaMbLE of SparLox83R produces versatile genome-wide genomic rearrangements, including inter-chromosomal events. Moreover, when combined with synthetic chromosomes, SCRaMbLE of hetero-diploids with SparLox83R leads to increased diversity of genomic rearrangements and relatively faster evolution of traits compared to hetero-diploids only with wild-type chromosomes. Analysis of the SCRaMbLEd strain with increased tolerance to nocodazole demonstrates that genomic rearrangements can perturb the transcriptome and 3D genome structure and consequently impact phenotypes. In summary, a genome with sparsely distributed loxPsym sites can serve as a powerful tool for studying the consequence of genomic rearrangements and accelerating strain engineering in Saccharomyces cerevisiae.

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Language(s): eng - English
 Dates: 2024-01-26
 Publication Status: Issued
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 Rev. Type: Peer
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 15 (1) Sequence Number: 770 Start / End Page: - Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723