4E-BP1 and S6K1: translational integration sites for nutritional and hormonal information in muscle

被引:232
作者
Shah, OJ [1 ]
Anthony, JC [1 ]
Kimball, SR [1 ]
Jefferson, LS [1 ]
机构
[1] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2000年 / 279卷 / 04期
关键词
eukaryotic initiation factor 4E binding protein; 70-kDa ribosomal protein S6 kinase; translation initiation;
D O I
10.1152/ajpendo.2000.279.4.E715
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maintenance of cellular protein stores in skeletal muscle depends on a tightly regulated synthesis-degradation equilibrium that is conditionally modulated under an extensive range of physiological and pathophysiological circumstances. Recent studies have established the initiation phase of mRNA translation as a pivotal site of regulation for global rates of protein synthesis, as well as a site through which the synthesis of specific proteins is controlled. The protein synthetic pathway is exquisitely sensitive to the availability of hormones and nutrients and employs a comprehensive integrative strategy to interpret the information provided by hormonal and nutritional cues. The translational repressor, eukaryotic initiation factor 4E binding protein 1 (4E-BP1), and the 70-kDa ribosomal protein S6 kinase (S6K1) have emerged as important components of this strategy, and together they coordinate the behavior of both eukaryotic initiation factors and the ribosome. This review discusses the role of 4E-BP1 and S6K1 in translational control and outlines the mechanisms through which hormones and nutrients effect changes in mRNA translation through the influence of these translational effectors.
引用
收藏
页码:E715 / E729
页数:15
相关论文
共 134 条
[1]   Atypical protein kinase Cλ binds and regulates p70 S6 kinase [J].
Akimoto, K ;
Nakaya, M ;
Yamanaka, T ;
Tanaka, J ;
Matsuda, S ;
Weng, QP ;
Avruch, J ;
Ohno, S .
BIOCHEMICAL JOURNAL, 1998, 335 :417-424
[2]   3 Phosphoinositide-dependent protein kinase 1 (PDK1) phosphorylates and activates the p70 S6 kinase in vivo and in vitro [J].
Alessi, DR ;
Kozlowski, MT ;
Weng, QP ;
Morrice, N ;
Avruch, J .
CURRENT BIOLOGY, 1998, 8 (02) :69-81
[3]   Translocation of PDK-1 to the plasma membrane is important in allowing PDK-1 to activate protein kinase B [J].
Anderson, KE ;
Coadwell, J ;
Stephens, LR ;
Hawkins, PT .
CURRENT BIOLOGY, 1998, 8 (12) :684-691
[4]   Orally administered leucine stimulates protein synthesis in skeletal muscle of postabsorptive rats in association with increased elF4F formation [J].
Anthony, JC ;
Anthony, TG ;
Kimball, SR ;
Vary, TC ;
Jefferson, LS .
JOURNAL OF NUTRITION, 2000, 130 (02) :139-145
[5]   PHAS-I phosphorylation in response to foetal bovine serum (FBS) is regulated by an ERK1/ERK2-independent and rapamycin-sensitive pathway in 3T3-L1 adipocytes [J].
Arnott, CH ;
Atkinson, PGP ;
Sale, EM ;
Sale, GJ .
FEBS LETTERS, 1997, 406 (1-2) :179-183
[6]   Insulin signal transduction through protein kinase cascades [J].
Avruch, J .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 182 (1-2) :31-48
[7]  
Azpiazu I, 1996, J BIOL CHEM, V271, P5033
[8]   PDK1 acquires PDK2 activity in the presence of a synthetic peptide derived from the carboxyl terminus of PRK2 [J].
Balendran, A ;
Casamayor, A ;
Deak, M ;
Paterson, A ;
Gaffney, P ;
Currie, R ;
Downes, CP ;
Alessi, DR .
CURRENT BIOLOGY, 1999, 9 (08) :393-404
[9]   TOR controls translation initiation and early G1 progression in yeast [J].
Barbet, NC ;
Schneider, U ;
Helliwell, SB ;
Stansfield, I ;
Tuite, MF ;
Hall, MN .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (01) :25-42
[10]   An abundant supply of amino acids enhances the metabolic effect of exercise on muscle protein [J].
Biolo, G ;
Tipton, KD ;
Klein, S ;
Wolfe, RR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (01) :E122-E129