Synthesis and turn-over of the replicative Cdc6 protein during the HeLa cell cycle

被引:9
作者
Biermann, E [1 ]
Baack, M [1 ]
Kreitz, S [1 ]
Knippers, R [1 ]
机构
[1] Univ Konstanz, Dept Biol, D-78457 Constance, Germany
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2002年 / 269卷 / 03期
关键词
cell cycle; DNA replication; hCdc6; phosphorylation; turn-over;
D O I
10.1046/j.0014-2956.2001.02746.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
The human replication protein Cdc6p is translocated from its chromatin sites to the cytoplasm during the replication phase (S phase) of the cell cycle. However, the amounts of Cdc6p on chromatin remain high during S phase implying either that displaced Cdc6p can rebind to chromatin. or that Cdc6p is synthesized de novo. We have performed metabolic labeling experiments and determined that [S-35]methionine is incorporated into Cdc6p at similar rates during the G1 phase and the S phase of the cell cycle. Newly synthesized Cdc6p associates with chromatin. Pulse-chase experiments show that chromatin-bound newly synthesized Cdc6p has a half life of 2 4 h. The results indicate that, once bound to chromatin, pulse-labeled nook Cdc6p behaves just as old Cdc6p: it dissociates and eventually disappears from the nucleus. The data Suggest a surprisingly dynamic behaviour of Cdc6p in the HeLa cell cycle.
引用
收藏
页码:1040 / 1046
页数:7
相关论文
共 41 条
[31]   CDC6 IS AN UNSTABLE PROTEIN WHOSE DE-NOVO SYNTHESIS IN G(1) IS IMPORTANT FOR THE ONSET OF S-PHASE AND FOR PREVENTING A REDUCTIONAL ANAPHASE IN THE BUDDING YEAST SACCHAROMYCES-CEREVISIAE [J].
PIATTI, S ;
LENGAUER, C ;
NASMYTH, K .
EMBO JOURNAL, 1995, 14 (15) :3788-3799
[32]   Activation of S-phase-promoting CDKs in late G(1) defines a ''point of no return'' after which Cdc6 synthesis cannot promote DNA replication in yeast [J].
Piatti, S ;
Bohm, T ;
Cocker, JH ;
Diffley, JFX ;
Nasmyth, K .
GENES & DEVELOPMENT, 1996, 10 (12) :1516-1531
[33]  
QUINTANA DG, 1999, FRONT BIOSCI, V4, P805, DOI DOI 10.2741/QUINTANA
[34]  
ROSE SM, 1984, J BIOL CHEM, V259, P8534
[35]   Human CDC6/Cdc18 associates with Orc1 and cyclin-cdk and is selectively eliminated from the nucleus at the onset of S phase [J].
Saha, P ;
Chen, JJ ;
Thome, KC ;
Lawlis, SJ ;
Hou, ZH ;
Hendricks, M ;
Parvin, JD ;
Dutta, A .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2758-2767
[36]   The Cdc6 protein is ubiquitinated in vivo for proteolysis in Saccharomyces cerevisiae [J].
Sánchez, M ;
Calzada, A ;
Bueno, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :9092-9097
[37]   Cdc6 protein causes premature entry into S phase in a mammalian cell-free system [J].
Stoeber, K ;
Mills, AD ;
Kubota, Y ;
Krude, T ;
Romanowski, P ;
Marheineke, K ;
Laskey, RA ;
Williams, GH .
EMBO JOURNAL, 1998, 17 (24) :7219-7229
[38]   The Cdc6p nucleotide-binding motif is required for loading Mcm proteins onto chromatin [J].
Weinreich, M ;
Liang, C ;
Stillman, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (02) :441-446
[39]   A human protein related to yeast Cdc6p [J].
Williams, RS ;
Shohet, RV ;
Stillman, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (01) :142-147
[40]   Inhibition of eukaryotic DNA replication by geminin binding to Cdt1 [J].
Wohlschlegel, JA ;
Dwyer, BT ;
Dhar, SK ;
Cvetic, C ;
Walter, JC ;
Dutta, A .
SCIENCE, 2000, 290 (5500) :2309-+