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人工合成基因组控制的细菌细胞的创建。

Creation of a bacterial cell controlled by a chemically synthesized genome.

机构信息

The J. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850, USA.

出版信息

Science. 2010 Jul 2;329(5987):52-6. doi: 10.1126/science.1190719. Epub 2010 May 20.

Abstract

We report the design, synthesis, and assembly of the 1.08-mega-base pair Mycoplasma mycoides JCVI-syn1.0 genome starting from digitized genome sequence information and its transplantation into a M. capricolum recipient cell to create new M. mycoides cells that are controlled only by the synthetic chromosome. The only DNA in the cells is the designed synthetic DNA sequence, including "watermark" sequences and other designed gene deletions and polymorphisms, and mutations acquired during the building process. The new cells have expected phenotypic properties and are capable of continuous self-replication.

摘要

我们报告了 1.08 兆碱基对的支原体支原体 JCVI-syn1.0 基因组的设计、合成和组装,该基因组从数字化的基因组序列信息开始,并将其移植到 M. capricolum 受体细胞中,以创建仅受合成染色体控制的新支原体细胞。细胞中唯一的 DNA 是设计的合成 DNA 序列,包括“水印”序列和其他设计的基因缺失和多态性,以及在构建过程中获得的突变。新细胞具有预期的表型特性,并且能够连续自我复制。

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