TY - JOUR
T1 - Core Fermentation (CoFe) granules focus coordinated glycolytic mRNA localization and translation to fuel glucose fermentation
AU - Morales Polanco, Fabián
AU - Bates, Christian
AU - Lui, Jennifer
AU - Casson, Joe
AU - Solari, Clara
AU - Pizzinga, Mariavittoria
AU - Forte, Gabbie
AU - Griffin, Claire
AU - Garner, Kirsten
AU - Burt, Harriet
AU - Dixon, Hannah
AU - Hubbard, Simon
AU - Portela, Paula
AU - Ashe, Mark
N1 - Funding Information:
We thank L. Berchowitz, J. Gerst, J. Chao, and R. Singer for reagents; P. March and S. Marsden for microscopy advice; and E. Linney for comments on the manuscript. FMP was supported by a CONICYT Becas Chile studentship ( 72140307 ). CB and MP were supported by Wellcome Trust (WT) PhD studentships ( 210002/Z/17/Z and 099732/Z/12/Z ). JL, CG, and GF were supported by a Biotechnology and Biological Sciences Research Council ( BBSRC ) project grant ( BB/K005979/1 ). JC and KG were supported by a BBSRC project grant ( BB/P018270/1 ). The Bioimaging microscopes used in this study were funded by grants from BBSRC , WT , and the University of Manchester Strategic Fund.
Publisher Copyright:
© 2021
PY - 2021/2/19
Y1 - 2021/2/19
N2 - Glycolysis is a fundamental metabolic pathway for glucose catabolism across biology, and glycolytic enzymes are among the most abundant proteins in cells. Their expression at such levels provides a particular challenge. Here we demonstrate that the glycolytic mRNAs are localized to granules in yeast and human cells. Detailed live cell and smFISH studies in yeast show that the mRNAs are actively translated in granules, and this translation appears critical for the localization. Furthermore, this arrangement is likely to facilitate the higher level organization and control of the glycolytic pathway. Indeed, the degree of fermentation required by cells is intrinsically connected to the extent of mRNA localization to granules. On this basis, we term these granules, core fermentation (CoFe) granules; they appear to represent translation factories, allowing high-level coordinated enzyme synthesis for a critical metabolic pathway.
AB - Glycolysis is a fundamental metabolic pathway for glucose catabolism across biology, and glycolytic enzymes are among the most abundant proteins in cells. Their expression at such levels provides a particular challenge. Here we demonstrate that the glycolytic mRNAs are localized to granules in yeast and human cells. Detailed live cell and smFISH studies in yeast show that the mRNAs are actively translated in granules, and this translation appears critical for the localization. Furthermore, this arrangement is likely to facilitate the higher level organization and control of the glycolytic pathway. Indeed, the degree of fermentation required by cells is intrinsically connected to the extent of mRNA localization to granules. On this basis, we term these granules, core fermentation (CoFe) granules; they appear to represent translation factories, allowing high-level coordinated enzyme synthesis for a critical metabolic pathway.
KW - cell biology
KW - molecular biology
UR - http://www.scopus.com/inward/record.url?scp=85100115181&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2021.102069
DO - 10.1016/j.isci.2021.102069
M3 - Article
C2 - 33554071
SN - 2589-0042
VL - 24
SP - 1
EP - 18
JO - iScience
JF - iScience
IS - 2
M1 - 102069
ER -