Perspectives on the DNA damage and replication checkpoint responses in Saccharomyces cerevisiae

被引:63
作者
Putnam, Christopher D. [1 ]
Jaehnig, Eric J.
Kolodner, Richard D.
机构
[1] Univ Calif San Diego, Ludwig Inst Canc Res, Dept Med, Sch Med, La Jolla, CA 92093 USA
关键词
Cell cycle checkpoint; DNA damage; DNA repair; Genome stability; Positive feedback; Transcriptional response; S-PHASE CHECKPOINT; DOUBLE-STRAND BREAKS; CELL-CYCLE; BUDDING YEAST; POSITIVE FEEDBACK; TYROSINE PHOSPHORYLATION; HOMOLOGOUS RECOMBINATION; H2A PHOSPHORYLATION; PHOSPHATASE COMPLEX; DOMAIN INTERACTION;
D O I
10.1016/j.dnarep.2009.04.021
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The DNA damage and replication checkpoints are believed to primarily slow the progression of the cell cycle to allow DNA repair to occur. Here we summarize known aspects of the Saccharomyces cerevisiae checkpoints including how these responses are integrated into downstream effects on the cell cycle, chromatin, DNA repair, and cytoplasmic targets. Analysis of the transcriptional response demonstrates that it is far more complex and less relevant to the repair of DNA damage than the bacterial SOS response. We also address more speculative questions regarding potential roles of the checkpoint during the normal S-phase and how current evidence hints at a checkpoint activation mechanism mediated by positive feedback that amplifies initial damage signals above a minimum threshold. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:974 / 982
页数:9
相关论文
共 137 条
[1]   Two distinct pathways for inhibiting Pds1 ubiquitination in response to DNA damage [J].
Agarwal, R ;
Tang, ZY ;
Yu, HT ;
Cohen-Fix, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (45) :45027-45033
[2]   The non-homologous end-joining protein Nej1p is a target of the DNA damage checkpoint [J].
Ahnesorg, Peter ;
Jackson, Stephen P. .
DNA REPAIR, 2007, 6 (02) :190-201
[3]   Mrc1 transduces signals of DNA replication stress to activate Rad53 [J].
Alcasabas, AA ;
Osborn, AJ ;
Bachant, J ;
Hu, FH ;
Werler, PJH ;
Bousset, K ;
Furuya, K ;
Diffley, JFX ;
Carr, AM ;
Elledge, SJ .
NATURE CELL BIOLOGY, 2001, 3 (11) :958-965
[4]   THE SAD1/RAD53 PROTEIN-KINASE CONTROLS MULTIPLE CHECKPOINTS AND DNA DAMAGE-INDUCED TRANSCRIPTION IN YEAST [J].
ALLEN, JB ;
ZHOU, Z ;
SIEDE, W ;
FRIEDBERG, EC ;
ELLEDGE, SJ .
GENES & DEVELOPMENT, 1994, 8 (20) :2401-2415
[5]   REGULATION OF P34CDC28 TYROSINE PHOSPHORYLATION IS NOT REQUIRED FOR ENTRY INTO MITOSIS IN SACCHAROMYCES-CEREVISIAE [J].
AMON, A ;
SURANA, U ;
MUROFF, I ;
NASMYTH, K .
NATURE, 1992, 355 (6358) :368-371
[6]   DPB11, WHICH INTERACTS WITH DNA-POLYMERASE II(EPSILON) IN SACCHAROMYCES-CEREVISIAE, HAS A DUAL ROLE IN S-PHASE PROGRESSION AND AT A CELL-CYCLE CHECKPOINT [J].
ARAKI, H ;
LEEM, SH ;
PHONGDARA, A ;
SUGINO, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11791-11795
[7]   Strength in numbers: preventing rereplication via multiple mechanisms in eukaryotic cells [J].
Arias, Emily E. ;
Walter, Johannes C. .
GENES & DEVELOPMENT, 2007, 21 (05) :497-518
[8]   The functions of budding yeast Sae2 in the DNA damage response require Mec1- and Tel1-dependent phosphorylation [J].
Baroni, E ;
Viscardi, V ;
Cartagena-Lirola, H ;
Lucchini, G ;
Longhese, MP .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (10) :4151-4165
[9]   Evidence of meiotic crossover control in Saccharomyces cerevisiae through Mec1-mediated phosphorylation of replication protein A [J].
Bartrand, AJ ;
Iyasu, D ;
Marinco, SM ;
Brush, GS .
GENETICS, 2006, 172 (01) :27-39
[10]   Direct kinase-to-kinase signaling mediated by the FHA phosphoprotein recognition domain of the Dun1 DNA damage checkpoint kinase [J].
Bashkirov, VI ;
Bashkirova, EV ;
Haghnazari, E ;
Heyer, WD .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (04) :1441-1452