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Signaling Pathways Involved in the Regulation of mRNA Translation
- Source :
- Molecular and Cellular Biology
- Publication Year :
- 2018
- Publisher :
- Informa UK Limited, 2018.
-
Abstract
- Translation is a key step in the regulation of gene expression and one of the most energy-consuming processes in the cell. In response to various stimuli, multiple signaling pathways converge on the translational machinery to regulate its function. To date, the roles of phosphoinositide 3-kinase (PI3K)/AKT and the mitogen-activated protein kinase (MAPK) pathways in the regulation of translation are among the best understood. Both pathways engage the mechanistic target of rapamycin (mTOR) to regulate a variety of components of the translational machinery. While these pathways regulate protein synthesis in homeostasis, their dysregulation results in aberrant translation leading to human diseases, including diabetes, neurological disorders, and cancer. Here we review the roles of the PI3K/AKT and MAPK pathways in the regulation of mRNA translation. We also highlight additional signaling mechanisms that have recently emerged as regulators of the translational apparatus.
- Subjects :
- 0301 basic medicine
MAPK/ERK pathway
mRNA translation
MNK
mRNA
Eukaryotic Initiation Factor-2
Mechanistic Target of Rapamycin Complex 1
Biology
Phosphatidylinositol 3-Kinases
03 medical and health sciences
Animals
Humans
RNA, Messenger
Molecular Biology
Protein kinase B
Mechanistic target of rapamycin
PI3K/AKT/mTOR pathway
Regulation of gene expression
TOR Serine-Threonine Kinases
RSK
EIF4E
translational control
Translation (biology)
Cell Biology
MAPK
protein phosphorylation
Cell biology
030104 developmental biology
Gene Expression Regulation
Protein Biosynthesis
eIF4E
mitogen-activated protein kinases
mTOR
biology.protein
Minireview
Signal transduction
Proto-Oncogene Proteins c-akt
signal transduction
Subjects
Details
- ISSN :
- 10985549
- Volume :
- 38
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Biology
- Accession number :
- edsair.doi.dedup.....89de21410110543d51f09b85c000e44f
- Full Text :
- https://doi.org/10.1128/mcb.00070-18