bioRxivSynthetic BiologyPreprint
Verification of genetic engineering in yeasts with nanopore whole genome sequencing
Joseph H. Collins, Kevin W. KeatingiD, Trent R. Jones, Shravani Balaji, Celeste B. Marsan, Marina Çomo, Zachary J. Newlon, Tom MitchelliD, Bryan BartleyiD, Aaron AdleriD, Nicholas RoehneriD, Eric M. YoungiD
Abstract
Yeast genomes can be assembled from sequencing data, but genome integrations and episomal plasmids often fail to be resolved with accuracy, completeness, and contiguity. Resolution of these features is critical for many synthetic biology applications, including strain quality control and identifying engineering in unknown samples. Here, we report an integrated workflow, named Prymetime, that uses sequencing reads from inexpensive NGS platforms, assembly and error correction software, and a list of synthetic biology parts to achieve accurate whole genome sequences of yeasts with engineering annotated. To build the workflow, we first determined which sequencing methods and software packages returned an accurate, complete, and contiguous genome of an engineered S. cerevisiae strain with two similar plasmids and an integrated pathway. We then developed a sequence feature annotation step that labels synthetic biology parts from a standard list of yeast engineering sequences or from a custom sequence list. We validated the workflow by sequencing a collection of 15 engineered yeasts built from different parent S. cerevisiae and nonconventional yeast strains. We show that each integrated pathway and episomal plasmid can be correctly assembled and annotated, even in strains that have part repeats and multiple similar plasmids. Interestingly, Prymetime was able to identify deletions and unintended integrations that were subsequently confirmed by other methods. Furthermore, the whole genomes are accurate, complete, and contiguous. To illustrate this clearly, we used a publicly available S. cerevisiae CEN.PK113 reference genome and the accompanying reads to show that a Prymetime genome assembly is equivalent to the reference using several standard metrics. Finally, we used Prymetime to resequence the nonconventional yeasts Y. lipolytica Po1f and K. phaffii CBS 7435, producing an improved genome assembly for each strain. Thus, our workflow can achieve accurate, complete, and contiguous whole genome sequences of yeast strains before and after engineering. Therefore, Prymetime enables NGS-based strain quality control through assembly and identification of engineering features.
- organism: yeast
- assay: whole-genome sequencing
- research focus: genome assembly
- research focus: variant calling
- research focus: benchmarking
- research focus: database / resource
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer
Benjamin Istace, Anne Friedrich, … Jean-Marc Aury·bioRxiv·Jul 28, 2016
- Combining fusion of cells with CRISPR-Cas9 editing for the cloning of large DNA fragments or complete bacterial genomes in yeast.
Gabrielle Guesdon, Géraldine Gourgues, … Carole Lartigue·ACS Synthetic BiologyPeer-reviewed·Oct 16, 2023
- CReasPy-cloning: a method for simultaneous cloning and engineering of megabase-sized genomes in yeast using the CRISPR-Cas9 system
E. Ruiz, V. Talenton, … C. Lartigue·bioRxiv·May 29, 2019
- Fast and inexpensive whole genome sequencing library preparation from intact yeast cells
Sibylle Chantal Vonesch, Shengdi Li, … and Lars M Steinmetz·G3 Genes Genomes GeneticsPeer-reviewed·Nov 27, 2020
- Nanopore sequencing enables near-complete de novo assembly of Saccharomyces cerevisiae reference strain CEN.PK113-7D
Alex Salazar, Arthur R. Gorter de Vries, … Thomas Abeel·FEMS Yeast ResearchPeer-reviewed·Sep 11, 2017
- ACtivE: Assembly and CRISPR-targeted in vivo Editing for Yeast Genome Engineering Using Minimum Reagents and Time
Koray Malcı, Nestor Jonguitud‐Borrego, … Leonardo Rios‐Solis·ACS Synthetic BiologyPeer-reviewed·Oct 17, 2022