The role of c-myc in regulation of translation initiation

被引:130
作者
Schmidt, EV
机构
[1] Massachusetts Gen Hosp, Canc Res Ctr, Boston, MA 02114 USA
[2] MassGen Hosp Children, Boston, MA 02114 USA
关键词
translational; control; eIF4E; ribosomal synthesis; rDNA transcription;
D O I
10.1038/sj.onc.1207548
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
Translation initiation is important for the regulation of both cell growth and cell division. It is uniquely poised to coordinate overall cell proliferation by its effects on both growth and division. A number of translation initiation factors are transcriptional targets of c-myc in a variety of assays. In particular, the mRNA cap-binding protein eIF4E has a myc-binding sequence in its promoter that is myc responsive in reporter assays and contains a high-affinity myc-binding site in chromosome immunoprecipitation experiments. Several differential expression screens have demonstrated altered levels of eIF4E, along with several other translation initiation factors, in response to alterations of c-myc levels. The potential for eIF4E and other translational control elements to mediate myc's transforming functions is particularly important because eIF4E is itself a known oncogenic factor. The ability of translation initiation factors to affect both cell division control and cell growth control coincides with myc's remarkable effects on both cell growth and cell division.
引用
收藏
页码:3217 / 3221
页数:5
相关论文
共 66 条
[1]  
Amati B., 2001, BIOCHIM BIOPHYS ACTA, V1471, P135
[2]  
Baserga R, 1985, BIOL CELL REPROD
[3]   THE ORNITHINE DECARBOXYLASE GENE IS A TRANSCRIPTIONAL TARGET OF C-MYC [J].
BELLOFERNANDEZ, C ;
PACKHAM, G ;
CLEVELAND, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7804-7808
[4]   SEQUENCE-SPECIFIC DNA-BINDING BY THE C-MYC PROTEIN [J].
BLACKWELL, TK ;
KRETZNER, L ;
BLACKWOOD, EM ;
EISENMAN, RN ;
WEINTRAUB, H .
SCIENCE, 1990, 250 (4984) :1149-1151
[5]   N-myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis [J].
Boon, K ;
Caron, HN ;
van Asperen, R ;
Valentijn, L ;
Hermus, MC ;
van Sluis, P ;
Roobeek, I ;
Weis, I ;
Voûte, PA ;
Schwab, M ;
Versteeg, R .
EMBO JOURNAL, 2001, 20 (06) :1383-1393
[6]   Mammalian unfolded protein response inhibits cyclin D1 translation and cell-cycle progression [J].
Brewer, JW ;
Hendershot, LM ;
Sherr, CJ ;
Diehl, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8505-8510
[7]   c-myc null cells misregulate cad and gadd45 but not other proposed c-Myc targets [J].
Bush, A ;
Mateyak, M ;
Dugan, K ;
Obaya, A ;
Adachi, S ;
Sedivy, J ;
Cole, M .
GENES & DEVELOPMENT, 1998, 12 (24) :3797-3802
[8]   Expression analysis with oligonucleotide microarrays reveals that MYC regulates genes involved in growth, cell cycle, signaling, and adhesion [J].
Coller, HA ;
Grandori, C ;
Tamayo, P ;
Colbert, T ;
Lander, ES ;
Eisenman, RN ;
Golub, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3260-3265
[9]   c-Myc is required for the glucose-mediated induction of metabolic enzyme genes [J].
Collier, JJ ;
Doan, TTT ;
Daniels, MC ;
Schurr, JR ;
Kolls, JK ;
Scott, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6588-6595
[10]  
DUNCAN R, 1985, J BIOL CHEM, V260, P5486