Distinguished Professor at the J. Craig Venter InstituteView Slides
Clyde’s team 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 more than one hundred genes with unknown, or poorly defined, biological functions. Progress in defining the functions of these genes will be discussed. JCVI-syn3.0 is a versatile platform for investigating the core functions of life and for exploring whole-genome design.
Has been canceled due to the coronavirus pandemic.
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