Cell-cycle-dependent regulation of the human and mouse Tome-1 promoters

被引:30
作者
Yoshida, K [1 ]
机构
[1] Meiji Univ, Fac Agr, Dept Life Sci, Tama Ku, Kawasaki, Kanagawa 2148571, Japan
来源
FEBS LETTERS | 2005年 / 579卷 / 06期
关键词
Tome-1; promoter; cell-cycle-dependent element; gene transcription;
D O I
10.1016/j.febslet.2005.01.055
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
Tome-1, which refers to a trigger of mitotic entry 1, mediates the destruction of the mitosis-inhibitory kinase, Wee1, via the E3 ligase, SCF. In turn, Tome-1 itself is targeted for degradation by APC in the G1 phase of the cell cycle. In the present study, we analyzed the human and mouse Tome-1 promoter regions. Using synchronized cultures of NIH3T3 cells transfected with Tome-1 promoter/luciferase constructs, we showed that the promoter activity of Tome-1 is activated at the G2/M phase. Using various Tome-1 promoter/luciferase constructs, we showed that the CCAAT box located upstream of the transcription initiation site is important for the basal promoter activity. We identified a repressor element (cell-cycle-dependent element/cell cycle gene homology region) in the vicinity of the transcription start site, and mutations within this element diminished the cell-cycle-dependent transcriptional regulation of Tome-1. (C) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1488 / 1492
页数:5
相关论文
共 21 条
[1]   Tome-1, a trigger of mitotic entry, is degraded during G1 via the APC [J].
Ayad, NG ;
Rankin, S ;
Murakami, M ;
Jebanathirajah, J ;
Gygi, S ;
Kirschner, MW .
CELL, 2003, 113 (01) :101-113
[2]  
Bennett JD, 1996, ONCOGENE, V13, P1073
[3]   A CDE/CHR tandem element regulates cell cycle-dependent repression of cyclin B2 transcription [J].
Dohna, CLZ ;
Brandeis, M ;
Berr, F ;
Mössner, J ;
Engeland, K .
FEBS LETTERS, 2000, 484 (02) :77-81
[4]   A single cell cycle genes homology region (CHR) controls cell cycle-dependent transcription of the cdc25C phosphatase gene and is able to cooperate with E2F or Sp1/3 sites [J].
Haugwitz, U ;
Wasner, M ;
Wiedmann, M ;
Spiesbach, K ;
Rother, K ;
Mössner, J ;
Engeland, K .
NUCLEIC ACIDS RESEARCH, 2002, 30 (09) :1967-1976
[5]  
Huet X, 1996, MOL CELL BIOL, V16, P3789
[6]   Mitotic entry: Tipping the balance [J].
Kraft, C .
CURRENT BIOLOGY, 2003, 13 (11) :R445-R446
[7]  
Li FZ, 1999, CANCER RES, V59, P3143
[8]   Tome-1, wee1, and the onset of mitosis: Coupled destruction for timely entry [J].
Lim, HH ;
Surana, U .
MOLECULAR CELL, 2003, 11 (04) :845-846
[9]   Cell cycle-regulated repression of B-myb transcription: Cooperation of an E2F site with a contiguous corepressor element [J].
Liu, NS ;
Lucibello, FC ;
Zwicker, J ;
Engeland, K ;
Muller, R .
NUCLEIC ACIDS RESEARCH, 1996, 24 (15) :2905-2910
[10]   PERIODIC CDC25C TRANSCRIPTION IS MEDIATED BY A NOVEL CELL-CYCLE-REGULATED REPRESSOR ELEMENT (CDE) [J].
LUCIBELLO, FC ;
TRUSS, M ;
ZWICKER, J ;
EHLERT, F ;
BEATO, M ;
MULLER, R .
EMBO JOURNAL, 1995, 14 (01) :132-142