Translational control during mitosis

被引:43
作者
Le Breton, M [1 ]
Cormier, P [1 ]
Bellé, R [1 ]
Mulner-Lorillon, O [1 ]
Morales, J [1 ]
机构
[1] Stn Biol Roscoff, UPMC, CNRS, UMR 7150,Equipe Cycle Cellulaire & Dev, F-29682 Roscoff, France
关键词
translation; mitosis; CDK1; cyclin B complex;
D O I
10.1016/j.biochi.2005.04.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Translation is now recognized as an important process in the regulation of gene expression. During the cell cycle, translation is tightly regulated. Protein synthesis is necessary for entry into and progression through mitosis and conversely, modifications of translational activity are observed during the cell cycle. This review focuses on translational control during mitosis (or M-phase) and the role of CDK1/cyclin B, the universal cell cycle regulator implicated in the G2/M transition, in protein synthesis regulation. (C) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:805 / 811
页数:7
相关论文
共 68 条
[1]
Symplekin and xGLD-2 are required for CPEB-mediated cytoplasmic polyadenylation [J].
Barnard, DC ;
Ryan, K ;
Manley, JL ;
Richter, JD .
CELL, 2004, 119 (05) :641-651
[2]
BONNEAU AM, 1987, J BIOL CHEM, V262, P11134
[3]
Sea urchin elongation factor 1δ (EF1δ) and evidence for cell cycle-directed localization changes of a sub-fraction of the protein at M phase [J].
Boulben, S ;
Monnier, A ;
Le Breton, M ;
Morales, J ;
Cormier, P ;
Bellé, R ;
Mulner-Lorillon, O .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (10) :2178-2188
[4]
INCREASED PHOSPHORYLATION OF ELONGATION FACTOR-II DURING MITOSIS IN TRANSFORMED HUMAN AMNION CELLS CORRELATES WITH A DECREASED RATE OF PROTEIN-SYNTHESIS [J].
CELIS, JE ;
MADSEN, P ;
RYAZANOV, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4231-4235
[5]
Cytoplasmic polyadenylation element (CPE)- and CPE-binding protein (CPEB)-independent mechanisms regulate early class maternal mRNA translational activation in Xenopus oocytes [J].
Charlesworth, A ;
Cox, LL ;
MacNicol, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (17) :17650-17659
[6]
Insulin and prolactin synergistically stimulate β-casein messenger ribonucleic acid translation by cytoplasmic polyadenylation [J].
Choi, KM ;
Barash, I ;
Rhoads, RE .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (07) :1670-1686
[7]
Targets and mechanisms for the regulation of translation in malignant transformation [J].
Clemens, MJ .
ONCOGENE, 2004, 23 (18) :3180-3188
[8]
Inhibition of poly(A) polymerase requires p34cdc2/cyclin B phosphorylation of multiple consensus and non-consensus sites [J].
Colgan, DF ;
Murthy, KG ;
Zhao, W ;
Prives, C ;
Manley, JL .
EMBO JOURNAL, 1998, 17 (04) :1053-1062
[9]
Cormier Patrick, 2003, Prog Cell Cycle Res, V5, P469
[10]
Identification and characterization of a novel cell cycle-regulated internal ribosome entry site [J].
Cornelis, S ;
Bruynooghe, Y ;
Denecker, G ;
Van Huffel, S ;
Tinton, S ;
Beyaert, R .
MOLECULAR CELL, 2000, 5 (04) :597-605