Transcriptional regulation of E2F-1 and eIF-2 genes by α-Pal:: a potential mechanism for coordinated regulation of protein synthesis, growth, and the cell cycle

被引:16
作者
Efiok, BJS [1 ]
Safer, B [1 ]
机构
[1] NHLBI, Lab Mol Hematol, Sect Prot & RNA Biosynth, NIH, Bethesda, MD 20892 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2000年 / 1495卷 / 01期
关键词
alpha-Pal; E2F-1; apoptosis; cell-cycle;
D O I
10.1016/S0167-4889(99)00138-X
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
alpha-Pal regulates the basal transcription of the alpha and beta subunits of eukaryotic initiation factor two (eIF-2), a rate-limiting enzyme for the initiation of protein biosynthesis. We recently showed that its global function may be to modulate the expression of key metabolic genes in response to cellular proliferation. In this paper, we examined a potential molecular mechanism by which alpha-Pal may achieve this function. When overexpressed, alpha-Pal upregulated protein synthesis and growth, but downregulated the cell cycle. The mechanism for the increased protein synthesis and growth appeared to be a transcriptional upregulation of the eIF-2 alpha and eIF-2 beta genes. The mechanism for the cell cycle downregulation appeared to be a transcriptional downregulation of E2F-1, a transcription factor that regulates genes required for cell cycle progression beyond the G1/S interphase. Specifically, an apparently modified species of alpha-Pal bound to the eIF-2 promoters and induced transcriptional upregulation, whereas, an apparently unmodified species of the alpha-Pal bound to the E2F-1 promoter and induced transcriptional downregulation, By this mechanism, alpha-Pal may participate in coordinating the regulation of global protein synthesis, growth and the cell cycle; a regulation that is essential to cellular differentiation. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 68
页数:18
相关论文
共 57 条
[1]  
Adams PD, 1996, CURR TOP MICROBIOL, V208, P79
[2]  
Alberts B, 1994, MOL BIOL CELL, P864
[3]   BOTH P16 AND P21 FAMILIES OF CYCLIN-DEPENDENT KINASE (CDK) INHIBITORS BLOCK THE PHOSPHORYLATION OF CYCLIN-DEPENDENT KINASES BY THE CDK-ACTIVATING KINASE [J].
APRELIKOVA, O ;
XIONG, Y ;
LIU, ET .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (31) :18195-18197
[4]  
Ausubel FA, 1995, CURRENT PROTOCOLS MO
[5]  
CALZONE FJ, 1991, DEVELOPMENT, V112, P335
[6]   Genomic cloning and characterization of the human eukaryotic initiation factor-2β promoter [J].
Chiorini, JA ;
Miyamoto, S ;
Harkin, SJ ;
Safer, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (07) :4195-4201
[7]   Requirement of p27(Kip1) for restriction point control of the fibroblast cell cycle [J].
Coats, S ;
Flanagan, WM ;
Nourse, J ;
Roberts, JM .
SCIENCE, 1996, 272 (5263) :877-880
[8]  
Cobrinik D, 1996, CURR TOP MICROBIOL, V208, P31
[9]   INCREASED ELF-2-ALPHA EXPRESSION IN MITOGEN-ACTIVATED PRIMARY LYMPHOCYTES-T [J].
COHEN, RB ;
BOAL, TR ;
SAFER, B .
EMBO JOURNAL, 1990, 9 (12) :3831-3837
[10]  
CORBEIL HB, 1995, ONCOGENE, V11, P909