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Cell Signaling in Protein Synthesis: Ribosome Biogenesis and Translation Initiation and Elongation
被引:64
|作者:
Mahoney, Sarah J.
[1
,2
]
Dempsey, Jamie M.
[1
,2
]
Blenis, John
[1
]
机构:
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA
来源:
TRANSLATIONAL CONTROL IN HEALTH AND DISEASE
|
2009年
/
90卷
关键词:
RNA-POLYMERASE-III;
CASEIN KINASE-II;
CAP-BINDING PROTEIN;
GUANINE-NUCLEOTIDE EXCHANGE;
PHORBOL ESTERS STIMULATE;
GLYCOGEN-SYNTHASE KINASE;
TUMOR-SUPPRESSOR PDCD4;
MR 100,000 SUBSTRATE;
DOUBLE-STRANDED-RNA;
RICH AKT SUBSTRATE;
D O I:
10.1016/S1877-1173(09)90002-3
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Protein synthesis is a highly energy-consuming process that must be tightly regulated. Signal transduction cascades respond to extracellular and intracellular cues to phosphorylate proteins involved in ribosomal biogenesis and translation initiation and elongation. These phosphorylation events regulate the timing and rate of translation of both specific and total mRNAs. Alterations in this regulation can result in dysfunction and disease. While many signaling pathways intersect to control protein synthesis, the mTOR and MAPK pathways appear to be key players. This chapter briefly reviews the mTOR and MAPK pathways and then focuses on individual phosphorylation events that directly control ribosome biogenesis and translation.
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页码:53 / 107
页数:55
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