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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 (Verlagsversion)
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 Urheber:
Cheng, Li1, Autor
Zhao, Shijun1, Autor
Li, Tianyi1, Autor
Hou, Sha1, Autor
Luo, Zhouqing1, Autor
Xu, Jinsheng1, Autor
Yu, Wenfei1, Autor
Jiang, Shuangying1, Autor
Monti, Marco1, Autor
Schindler, Daniel2, Autor                 
Zhang, Weimin1, Autor
Hou, Chunhui1, Autor
Ma, Yingxin1, Autor
Cai, Yizhi1, Autor
Boeke, Jef D.1, Autor
Dai, Junbiao1, Autor
Affiliations:
1external, ou_persistent22              
2Manchester Institute of Biotechnology, University of Manchester, UK, ou_persistent22              

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 Zusammenfassung: 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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Sprache(n): eng - English
 Datum: 2024-01-26
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: URI: https://doi.org/10.1038/s41467-023-44511-5
Anderer: Cheng2024
DOI: 10.1038/s41467-023-44511-5
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Titel: Nature Communications
  Kurztitel : Nat. Commun.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: London : Nature Publishing Group
Seiten: - Band / Heft: 15 (1) Artikelnummer: 770 Start- / Endseite: - Identifikator: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723