Mitochondrial volume fraction and translation duration impact mitochondrial mRNA localization and protein synthesis

Autor: Evelina Tutucci, Fan Xu, Susanne M. Rafelski, Joonhyuk Choi, Ximena G. Arceo, Brian M. Zid, Raghav Chanchani, Robert H. Singer, Jingwen Yu, Yang S. Chen, Matheus P. Viana, Tatsuhisa Tsuboi
Přispěvatelé: Systems Bioinformatics, AIMMS
Rok vydání: 2020
Předmět:
protein synthesis
RNA
Mitochondrial

Messenger
Cell
S. cerevisiae
Mitochondrion
Ribosome
cell biology
Gene expression
Protein biosynthesis
Biology (General)
0303 health sciences
Chemistry
General Neuroscience
030302 biochemistry & molecular biology
Translation (biology)
General Medicine
Chromosomes and Gene Expression
Mitochondrial
Cell biology
mitochondria
Fungal
medicine.anatomical_structure
Medicine
mRNA localization
Research Article
chromosomes
QH301-705.5
1.1 Normal biological development and functioning
Science
Saccharomyces cerevisiae
General Biochemistry
Genetics and Molecular Biology

Fungal Proteins
Mitochondrial Proteins
03 medical and health sciences
Underpinning research
Genetics
medicine
RNA
Messenger

030304 developmental biology
Messenger RNA
General Immunology and Microbiology
RNA
Fungal

Cell Biology
Cytoplasm
Protein Biosynthesis
gene expression
RNA
Generic health relevance
Mitochondrial Size
Biochemistry and Cell Biology
Zdroj: eLife, Vol 9 (2020)
Tsuboi, T, Viana, M P, Xu, F, Yu, J, Chanchani, R, Arceo, X G, Tutucci, E, Choi, J, Chen, Y S, Singer, R H, Rafelski, S M & Zid, B M 2020, ' Mitochondrial volume fraction and translation duration impact mitochondrial mRNA localization and protein synthesis ', eLife, vol. 9, e57814, pp. 1-24 . https://doi.org/10.7554/eLife.57814, https://doi.org/10.7554/ELIFE.57814
eLife, 9:e57814, 1-24. eLife Sciences Publications
eLife
ISSN: 2050-084X
Popis: Mitochondria are dynamic organelles that must precisely control their protein composition according to cellular energy demand. Although nuclear-encoded mRNAs can be localized to the mitochondrial surface, the importance of this localization is unclear. As yeast switch to respiratory metabolism, there is an increase in the fraction of the cytoplasm that is mitochondrial. Our data point to this change in mitochondrial volume fraction increasing the localization of certain nuclear-encoded mRNAs to the surface of the mitochondria. We show that mitochondrial mRNA localization is necessary and sufficient to increase protein production to levels required during respiratory growth. Furthermore, we find that ribosome stalling impacts mRNA sensitivity to mitochondrial volume fraction and counterintuitively leads to enhanced protein synthesis by increasing mRNA localization to mitochondria. This points to a mechanism by which cells are able to use translation elongation and the geometric constraints of the cell to fine-tune organelle-specific gene expression through mRNA localization.
Databáze: OpenAIRE