4.5 Article

Compacting a synthetic yeast chromosome arm

期刊

GENOME BIOLOGY
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-020-02232-8

关键词

Minimal genome; SCRaMbLE-based genome compaction; Essential gene array

资金

  1. National Key Research and Development Program of China [2018YFA0900100]
  2. Youth Innovation Promotion Association of the Chinese Academy of Sciences [2018396]
  3. National Natural Science Foundation of China [31725002, 31800069, 31800082]
  4. Shenzhen Key Laboratory of Synthetic Genomics [ZDSYS201802061806209]
  5. Shenzhen Science and Technology Program [KQTD20180413181837372]
  6. Guangdong Provincial Key Laboratory of Synthetic Genomics [2019B030301006]
  7. Bureau of International Cooperation, Chinese Academy of Sciences [172644KYSB20180022]
  8. BBSRC [R121730]
  9. Volkswagen Foundation the Life? Initiative Grant [94 771]

向作者/读者索取更多资源

We have developed an iterative SGC method with the aid of eArray as a generic yet effective tool to compact the synthetic yeast genome. The study demonstrates that at least 39 out of 65 nonessential genes in synXIIL can be removed collectively without affecting cell viability, and approximately 40% of the synthetic sequence is found to be dispensable for cell growth in specified conditions.
BackgroundRedundancy is a common feature of genomes, presumably to ensure robust growth under different and changing conditions. Genome compaction, removing sequences nonessential for given conditions, provides a novel way to understand the core principles of life. The synthetic chromosome rearrangement and modification by loxP-mediated evolution (SCRaMbLE) system is a unique feature implanted in the synthetic yeast genome (Sc2.0), which is proposed as an effective tool for genome minimization. As the Sc2.0 project is nearing its completion, we have begun to explore the application of the SCRaMbLE system in genome compaction.ResultsWe develop a method termed SCRaMbLE-based genome compaction (SGC) and demonstrate that a synthetic chromosome arm (synXIIL) can be efficiently reduced. The pre-introduced episomal essential gene array significantly enhances the compacting ability of SGC, not only by enabling the deletion of nonessential genes located in essential gene containing loxPsym units but also by allowing more chromosomal sequences to be removed in a single SGC process. Further compaction is achieved through iterative SGC, revealing that at least 39 out of 65 nonessential genes in synXIIL can be removed collectively without affecting cell viability at 30 degrees C in rich medium. Approximately 40% of the synthetic sequence, encoding 28 genes, is found to be dispensable for cell growth at 30 degrees C in rich medium and several genes whose functions are needed under specified conditions are identified.ConclusionsWe develop iterative SGC with the aid of eArray as a generic yet effective tool to compact the synthetic yeast genome.

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