| Literature DB >> 27013737 |
Clyde A Hutchison1, Ray-Yuan Chuang1, Vladimir N Noskov1, Nacyra Assad-Garcia1, Thomas J Deerinck2, Mark H Ellisman2, John Gill3, Krishna Kannan3, Bogumil J Karas1, Li Ma1, James F Pelletier4, Zhi-Qing Qi3, R Alexander Richter1, Elizabeth A Strychalski4, Lijie Sun1, Yo Suzuki1, Billyana Tsvetanova3, Kim S Wise1, Hamilton O Smith5, John I Glass1, Chuck Merryman1, Daniel G Gibson5, J Craig Venter5.
Abstract
We used whole-genome design and complete chemical synthesis to minimize the 1079-kilobase pair synthetic genome of Mycoplasma mycoides JCVI-syn1.0. An initial design, based on collective knowledge of molecular biology combined with limited transposon mutagenesis data, failed to produce a viable cell. Improved transposon mutagenesis methods revealed a class of quasi-essential genes that are needed for robust growth, explaining the failure of our initial design. Three cycles of design, synthesis, and testing, with retention of quasi-essential genes, produced JCVI-syn3.0 (531 kilobase pairs, 473 genes), which has a genome smaller than that of any autonomously replicating cell found in nature. JCVI-syn3.0 retains almost all genes involved in the synthesis and processing of macromolecules. Unexpectedly, it also contains 149 genes with unknown biological functions. JCVI-syn3.0 is a versatile platform for investigating the core functions of life and for exploring whole-genome design.Entities:
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Year: 2016 PMID: 27013737 DOI: 10.1126/science.aad6253
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728