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Asymmetric distribution of glucose transporter mRNA provides a growth advantage in yeast
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4500457
Author(s) Stahl, Timo; Hümmer, Stefan; Ehrenfeuchter, Nikolaus; Mittal, Nitish; Fucile, Geoffrey; Spang, Anne
Author(s) at UniBasel Ehrenfeuchter, Nikolaus
Spang, Anne
Year 2019
Year: comment 2019
Title Asymmetric distribution of glucose transporter mRNA provides a growth advantage in yeast
Journal The EMBO journal
Volume 38
Number 10
Pages / Article-Number e100373
Keywords cellular fitness, glucose transporter, mRNA localization, signaling, stress response
Abstract Asymmetric localization of mRNA is important for cell fate decisions in eukaryotes and provides the means for localized protein synthesis in a variety of cell types. Here, we show that hexose transporter mRNAs are retained in the mother cell of; S. cerevisiae; until metaphase-anaphase transition (MAT) and then are released into the bud. The retained mRNA was translationally less active but bound to ribosomes before MAT Importantly, when cells were shifted from starvation to glucose-rich conditions, HXT2 mRNA, but none of the other HXT mRNAs, was enriched in the bud after MAT This enrichment was dependent on the Ras/cAMP/PKA pathway, the APC ortholog Kar9, and nuclear segregation into the bud. Competition experiments between strains that only expressed one hexose transporter at a time revealed that; HXT2; only cells grow faster than their counterparts when released from starvation. Therefore, asymmetric distribution of HXT2 mRNA provides a growth advantage for daughters, who are better prepared for nutritional changes in the environment. Our data provide evidence that asymmetric mRNA localization is an important factor in determining cellular fitness.
Publisher EMBO Press
ISSN/ISBN 0261-4189 ; 1460-2075
URL https://www.biorxiv.org/content/early/2018/07/30/380279.full.pdf
edoc-URL https://edoc.unibas.ch/69924/
Full Text on edoc Available
Digital Object Identifier DOI 10.15252/embj.2018100373
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/30910878
ISI-Number WOS:000467961400011
Document type (ISI) Journal Article
 
   

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