About

Log in?

DTU users get better search results including licensed content and discounts on order fees.

Anyone can log in and get personalized features such as favorites, tags and feeds.

Log in as DTU user Log in as non-DTU user No thanks

DTU Findit

Journal article

Absolute Quantification of Protein and mRNA Abundances Demonstrate Variability in GeneSpecific Translation Efficiency in Yeast

From

Chalmers University of Technology1

University of Tartu2

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark3

Yeast Cell Factories, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark4

Protein synthesis is the most energy-consuming process in a proliferating cell, and understanding what controls protein abundances represents a key question in biology and biotechnology. We quantified absolute abundances of 5,354 mRNAs and 2,198 proteins in Saccharomyces cerevisiae under ten environmental conditions and protein turnover for 1,384 proteins under a reference condition.

The overall correlation between mRNA and protein abundances across all conditions was low (0.46), but for differentially expressed proteins (n = 202), the median mRNA-protein correlation was 0.88. We used these data to model translation efficiencies and found that they vary more than 400-fold between genes.

Non-linear regression analysis detected that mRNA abundance and translation elongation were the dominant factors controlling protein synthesis, explaining 61% and 15% of its variance. Metabolic flux balance analysis further showed that only mitochondrial fluxes were positively associated with changes at the transcript level.

The present dataset represents a crucial expansion to the current resources for future studies on yeast physiology.

Language: English
Year: 2017
Pages: 495-504
ISSN: 24054712 and 24054720
Types: Journal article
DOI: 10.1016/j.cels.2017.03.003
ORCIDs: Elsemman, Ibrahim

DTU users get better search results including licensed content and discounts on order fees.

Log in as DTU user

Access

Analysis