One Step Closer To Re-writing The First Synthetic Yeast Genome And Unravelling The Fundamental Building Blocks Of Life
Researchers have combined over seven synthetic chromosomes that were made in the lab into a single yeast cell, resulting in a strain with more than 50% synthetic DNA that survives and replicates similarly to wild yeast strains.
The team present the half-synthetic yeast November 8 in the journal Cell as part of a collection of papers across Cell, Molecular Cell, and Cell Genomics that showcase the Synthetic Yeast Genome Project (Sc2.0), a global consortium working to develop the first synthetic eukaryote genome from scratch. The team has now synthesized and debugged all sixteen yeast chromosomes.
“Our motivation is to understand the first principles of genome fundamentals by building synthetic genomes,” says co-author and synthetic biologist Patrick Yizhi Cai (@caiyizhi) of the University of Manchester, who is also senior author of two other papers in the collection. “The team has now re-written the operating system of the budding yeast, which opens up a new era of engineering biology—moving from tinkering a handful of genes to de novo design and construction of entire genomes.”
Though bacterial and viral genomes have been synthesized previously, this would be the first synthetic eukaryote genome, which introduces the complication of multiple chromosomes. The synthetic yeast is also a “designer” genome that differs substantially from the natural Saccharomyces cerevisiae (brewer’s or baker’s yeast) genome on which it is based.
“We decided that it was important to produce something that was very heavily modified from nature’s design,” says senior author and Sc2.0 leader Jef Boeke (@JefBoeke), a synthetic biologist at NYU Langone Health. “Our overarching aim was to build a yeast that can teach us new biology.”
To this end, the researchers removed chunks of non-coding DNA and repetitive elements that could be considered “junk,” added new snippets of DNA to help them more easily distinguish between synthesized and native genes, and introduced a built-in diversity generator called “SCRaMbLE” that shuffles the order of genes within and between chromosomes.
Here, we report the design, construction, and characterization of a tRNA neochromosome, a designer chromosome that functions as an additional, de novo counterpart to the native complement of Saccharomyces cerevisiae.
To increase genome stability, the team also removed many of the genes that encode transfer RNA (tRNA) and relocated them to an entirely new “neochromosome” consisting only of tRNA genes. “The tRNA neochromosome is the world’s first completely de novo synthetic chromosome,” says Cai. “Nothing like this exists in nature.”
Since the yeast genome is organized into sixteen chromosomes, the researchers began by assembling each chromosome independently to create sixteen partially synthetic yeast strains that each contained 15 natural chromosomes and one synthetic chromosome. The next challenge was to begin combining these synthetic chromosomes into a single yeast cell.
To do this, Boeke’s team started by using a method reminiscent of Mendel’s peas: essentially, the researchers interbred different partially synthetic yeast strains and then searched amongst their progeny for individuals carrying both synthetic chromosomes. Though effective, this method is very slow, but the team gradually consolidated all previously synthesized chromosomes—six full chromosomes and one chromosome arm—into a single cell. The resulting yeast strain was more than 31% synthetic, had normal morphology, and showed only slight growth defects compared to wild-type yeast.
To more efficiently transfer specific chromosomes between yeast strains, the researchers developed a new method called chromosome substitution that is discussed in another paper in the new collection. As a proof of concept, they used chromosome substitution to transfer a newly synthesized chromosome (chromosome IV, the largest of all the synthetic chromosomes), resulting in a yeast cell with 7.5 synthetic chromosomes that is more than 50% synthetic.
When the synthetic chromosomes were consolidated into a single yeast strain, the team detected several genetic defects or “bugs” that were invisible in yeast strains that only carried one synthetic chromosome. “We knew in principle that this might happen—that we might have a huge number of things that had tiny little effects and that, when you put them all together, it might result in death by a thousand cuts,” says Boeke.
Some of these bugs were simply due to the additive impact of having many tiny defects within the genome, while others involved genetic interactions between genes on the different synthetic chromosomes. The researchers were able to map and fix several of these bugs and increase the synthetic yeast’s fitness by using a method based on CRISPR/Cas9.
“We’ve now shown that we can consolidate essentially half of the genome with good fitness, which suggests that this is not going to be a big problem,” says Boeke. “And from debugging, we learn new twists on the rules of life.”
The next step will be to integrate the remaining synthetic chromosomes. “Now we’re just this far from the finish line of having all 16 chromosomes in a single cell,” says Boeke. “I like to call this the end of the beginning, not the beginning of the end, because that’s when we’re really going to be able to start shuffling that deck and producing yeast that can do things that we’ve never seen before.”
This research was supported by the National Science Foundation, the National Institutes of Health, the Laura and Isaac Perlmutter Cancer Center, and Volkswagen Stiftung.
Cell, Zhao et al., “Debugging and consolidating multiple synthetic chromosomes reveals combinatorial genetic interactions” https://cell.com/cell/fulltext/S092-8674(23)01079-6 DOI: 10.1016/j.cell.2023.09.025
Additional papers in the collection:
Cell, Schindler et al., “Design, Construction, and Functional Characterization of a tRNA Neochromosome in Yeast” https://www.cell.com/cell/fulltext/S0092-8674(23)01130-3 DOI: 10.1016/j.cell.2023.10.015
Cell Genomics, Shen et al., “Dissecting aneuploidy phenotypes by constructing Sc2.0 chromosome VII and SCRaMbLEing synthetic disomic yeast” https://www.cell.com/cell-genomics/fulltext/S2666-979X(23)00147-7 DOI: 10.1016/j.xgen.2023.100364
Cell Genomics, McCulloch et al., “Consequences of a telomerase-related fitness defect and chromosome substitution technology in yeast synIX strains” https://www.cell.com/cell-genomics/fulltext/S2666-979X(23)00245-8 DOI: 10.1016/j.xgen.2023.100419
Associated Preview article:
Cell Genomics, Taghon et al., “Rise of synthetic yeast: Charting courses to new applications” https://www.cell.com/cell-genomics/fulltext/S2666-979X(23)00273-2 DOI: 10.1016/j.xgen.2023.100438
Associated Voices article:
Cell Genomics, Nicholson et al., “A spotlight on global collaboration in the Sc2.0 yeast consortium” https://www.cell.com/cell-genomics/fulltext/S2666-979X(23)00276-8 DOI: 10.1016/j.xgen.2023.100441
Cell Genomics (@CellGenomics) is a new Gold open access journal from Cell Press. Publishing multidisciplinary research at the forefront of genetics and genomics, the journal aims to bring together diverse communities to advance genomics and its impact on biomedical science, precision medicine, and global and ecological health. Visit https://www.cell.com/cell-genomics/home. To receive Cell Press media alerts, please contact [email protected].
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