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Engineered yeast genomes accurately assembled from pure and mixed samples.
Collins, Joseph H; Keating, Kevin W; Jones, Trent R; Balaji, Shravani; Marsan, Celeste B; Çomo, Marina; Newlon, Zachary J; Mitchell, Tom; Bartley, Bryan; Adler, Aaron; Roehner, Nicholas; Young, Eric M.
Affiliation
  • Collins JH; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Keating KW; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Jones TR; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Balaji S; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Marsan CB; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Çomo M; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Newlon ZJ; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Mitchell T; Synthetic Biology, Raytheon BBN Technologies, Cambridge, MA, USA.
  • Bartley B; Synthetic Biology, Raytheon BBN Technologies, Cambridge, MA, USA.
  • Adler A; Synthetic Biology, Raytheon BBN Technologies, Cambridge, MA, USA.
  • Roehner N; Synthetic Biology, Raytheon BBN Technologies, Cambridge, MA, USA.
  • Young EM; Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA. emyoung@wpi.edu.
Nat Commun ; 12(1): 1485, 2021 03 05.
Article in En | MEDLINE | ID: mdl-33674578
ABSTRACT
Yeast whole genome sequencing (WGS) lacks end-to-end workflows that identify genetic engineering. Here we present Prymetime, a tool that assembles yeast plasmids and chromosomes and annotates genetic engineering sequences. It is a hybrid workflow-it uses short and long reads as inputs to perform separate linear and circular assembly steps. This structure is necessary to accurately resolve genetic engineering sequences in plasmids and the genome. We show this by assembling diverse engineered yeasts, in some cases revealing unintended deletions and integrations. Furthermore, the resulting whole genomes are high quality, although the underlying assembly software does not consistently resolve highly repetitive genome features. Finally, we assemble plasmids and genome integrations from metagenomic sequencing, even with 1 engineered cell in 1000. This work is a blueprint for building WGS workflows and establishes WGS-based identification of yeast genetic engineering.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Genetic Engineering / Genome, Fungal / Whole Genome Sequencing Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Genetic Engineering / Genome, Fungal / Whole Genome Sequencing Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2021 Document type: Article Affiliation country: