Control of cellular senescence by CPEB

被引:79
作者
Groisman, Irina
Ivshina, Maria
Marin, Veronica
Kennedy, Norman J.
Davis, Roger J.
Richter, Joel D. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
关键词
senescence; CPEB; translational control;
D O I
10.1101/gad.1438906
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytoplasmic polyadenylation element-binding protein (CPEB) is a sequence-specific RNA-binding protein that promotes polyadenylation-induced translation. While a CPEB knockout (KO) mouse is sterile but overtly normal, embryo fibroblasts derived from this mouse (MEFs) do not enter senescence in culture as do wild-type MEFs, but instead are immortal. Exogenous CPEB restores senescence in the KO MEFs and also induces precocious senescence in wild-type MEFs. CPEB cannot stimulate senescence in MEFs lacking the tumor suppressors p53, p19(ARF), or p16(INK4A); however, the mRNAs encoding these proteins are unlikely targets of CPEB since their expression is the same in wild-type and KO MEFs. Conversely, Ras cannot induce senescence in MEFs lacking CPEB, suggesting that it may lie upstream of CPEB. One target of CPEB regulation is myc mRNA, whose unregulated translation in the KO MEFs may cause them to bypass senescence. Thus, CPEB appears to act as a translational repressor protein to control myc translation and resulting cellular senescence.
引用
收藏
页码:2701 / 2712
页数:12
相关论文
共 54 条
[21]   Specificity of RNA binding by CPEB: Requirement for RNA recognition motifs and a novel zinc finger [J].
Hake, LE ;
Mendez, R ;
Richter, JD .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) :685-693
[22]   Translational control by neuroguidin, a eukaryotic initiation factor 4E and CPEB binding protein [J].
Jung, Mi-Young ;
Lorenz, Lori ;
Richter, Joel D. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (11) :4277-4287
[23]   Mammalian poly(A)-binding protein is a eukaryotic translation initiation factor, which acts via multiple mechanisms [J].
Kahvejian, A ;
Svitkin, YV ;
Sukarieh, R ;
M'Boutchou, MN ;
Sonenberg, N .
GENES & DEVELOPMENT, 2005, 19 (01) :104-113
[24]  
KARN J, 1989, ONCOGENE, V4, P773
[25]   Mammalian GLD-2 homologs are poly(A) polymerases [J].
Kwak, JE ;
Wang, LT ;
Ballantyne, S ;
Kimble, J ;
Wickens, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4407-4412
[26]   Contributions of myc to tumorigenesis [J].
Lutz, W ;
Leon, J ;
Eilers, M .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2002, 1602 (01) :61-71
[27]   Mammalian cyclin-dependent kinases [J].
Malumbres, M ;
Barbacid, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (11) :630-641
[28]  
Mateyak MK, 1999, MOL CELL BIOL, V19, P4672
[29]   Differential rnRNA translation and rneiotic progression require Cdc2-mediated CPEB destruction [J].
Mendez, R ;
Barnard, D ;
Richter, JD .
EMBO JOURNAL, 2002, 21 (07) :1833-1844
[30]   Phosphorylation of CPE binding factor by Eg2 regulates translation of c-mos mRNA [J].
Mendez, R ;
Hake, LE ;
Andresson, T ;
Littlepage, LE ;
Ruderman, JV ;
Richter, JD .
NATURE, 2000, 404 (6775) :302-307