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  Design, construction, and functional characterization of a tRNA neochromosome in yeast

Schindler, D., Walker, R. S., Jiang, S., Brooks, A. N., Wang, Y., Müller, C. A., et al. (2022). Design, construction, and functional characterization of a tRNA neochromosome in yeast. bioRxiv: the preprint server for biology, 2022.10.03.510608.

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Preprint
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 Creators:
Schindler, Daniel1, 2, Author                 
Walker, Roy S.K.3, Author
Jiang, Shuangying3, Author
Brooks, Aaron N.3, Author
Wang, Yun3, Author
Müller, Carolin A.3, Author
Cockram, Charlotte3, Author
Luo, Yisha3, Author
García, Alicia3, Author
Schraivogel, Daniel3, Author
Mozziconacci, Julien3, Author
Blount, Benjamin A.3, Author
Cai, Jitong3, Author
Ogunlana, Lois3, Author
Liu, Wei3, Author
Jönsson, Katarina3, Author
Abramczyk, Dariusz3, Author
Garcia-Ruiz, Eva3, Author
Turowski, Tomasz W.3, Author
Swidah, Reem3, Author
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Affiliations:
1Core Facility MPG MAXGenesys DNAfoundry, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266268              
2Manchester Institute of Biotechnology, University of Manchester, UK, ou_persistent22              
3external, ou_persistent22              

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 Abstract: 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. Intending to address one of the central design principles of the Sc2.0 project, the ∼190 kb tRNA neochromosome houses all 275 relocated nuclear tRNA genes. To maximize stability, the design incorporated orthogonal genetic elements from non-S. cerevisiae yeast species. Furthermore, the presence of 283 rox recombination sites enable an orthogonal SCRaMbLE system capable of adjusting tRNA abundance. Following construction, we obtained evidence of a potent selective force once the neochromosome was introduced into yeast cells, manifesting as a spontaneous doubling in cell ploidy. Furthermore, tRNA sequencing, transcriptomics, proteomics, nucleosome mapping, replication profiling, FISH and Hi-C were undertaken to investigate questions of tRNA neochromosome behavior and function. Its construction demonstrates the remarkable tractability of the yeast model and opens up new opportunities to directly test hypotheses surrounding these essential non-coding RNAs.HighlightsDe novo design, construction and functional characterization of a neochromosome containing all 275 nuclear tRNA genes of Saccharomyces cerevisiae.Increasing the copy number of the 275 highly expressed tRNA genes causes cellular burden, which the host cell likely buffers either by selecting for partial tRNA neochromosome deletions or by increasing its ploidy.The tRNA neochromosome can be chemically extracted and transformed into new strain backgrounds, enabling its transplantation into multi-synthetic chromosome strains to finalize the Sc2.0 strain.Comprehensive functional characterization does not pinpoint a singular cause for the cellular burden caused by the tRNA neochromosome, but does reveal novel insights into its tRNA and structural chromosome biology.Competing Interest StatementJef D. Boeke is a Founder and Director of CDI Labs, Inc., a Founder of and consultant to Neochromosome, Inc, a Founder, SAB member of and consultant to ReOpen Diagnostics, LLC and serves or served on the Scientific Advisory Board of the following: Sangamo, Inc., Modern Meadow, Inc., Rome Therapeutics, Inc., Sample6, Inc., Tessera Therapeutics, Inc. and the Wyss Institute.

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Language(s): eng - English
 Dates: 2022-01
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: No review
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Title: bioRxiv : the preprint server for biology
  Abbreviation : bioRxiv
Source Genre: Journal
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Pages: - Volume / Issue: - Sequence Number: 2022.10.03.510608 Start / End Page: - Identifier: ZDB: 2766415-6
CoNE: https://pure.mpg.de/cone/journals/resource/2766415-6