Control of Translation Initiation through Integration of Signals Generated by Hormones, Nutrients, and Exercise

• Published in: The Journal of biological chemistry Vol. 285; no. 38; pp. 29027 - 29032
• Main Authors: Kimball, Scot R., Jefferson, Leonard S.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 17.09.2010; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid; Animals; Exercise - physiology; Hormones - metabolism; Humans; Insulin; Mechanistic Target of Rapamycin Complex 1; Minireviews; Models, Biological; mTOR Complex (mTORC); Multiprotein Complexes; Muscle, Skeletal - metabolism; Protein Synthesis and Degradation; Proteins; Ribosome Subunits, Small, Eukaryotic - metabolism; RNA, Transfer, Met - metabolism; Signal Transduction - physiology; Skeletal Muscle; TOR Serine-Threonine Kinases; Transcription Factors - metabolism; Translation Initiation Factors; Translation Regulation; Amino Acid; mTOR Complex (mTORC); Skeletal Muscle; Translation Regulation; Insulin; Translation Initiation Factors
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.R110.137208

Control of translation initiation in a tissue of an intact mammalian organism is a highly complex process requiring the continuous integration of multiple positive and negative stimuli. For a tissue such as skeletal muscle, which has the capacity to undergo dramatic changes in size and protein content, translation initiation contributes importantly to the regulation of global rates of protein synthesis and is controlled by numerous stimuli, including those arising from nutrients and hormones in the circulating blood, as well as from contraction-induced signaling within the tissue. Many of the pathways conveying signals generated by these stimuli converge on mTORC1, a serine-threonine protein kinase that has been termed the nutrient and energy sensor of the cell and that plays a prominent role in the regulation of cell growth. Control of translation initiation by mTORC1 is mediated through phosphorylation of downstream targets that modulate the binding of mRNA to the 43 S preinitiation complex. Control of translation initiation is also mediated through modulation of binding of initiator methionyl-tRNA to the 40 S ribosomal subunit. Together, modulation of these two regulatory steps in translation initiation accounts in large part for changes in protein synthesis in skeletal muscle produced by the integration of inputs from hormones, nutrients, and exercise.