Eukaryotic MCM proteins: Beyond replication initiation

被引:457
作者
Forsburg, SL [1 ]
机构
[1] Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1128/MMBR.68.1.109-131.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The minichromosome maintenance (or MCM) protein family is composed of six related proteins that are conserved in all eukatyotes. They were first identified by genetic screens in yeast and subsequently analyzed in other experimental systems using molecular and biochemical methods. Early data led to the identification of MCMs as central players in the initiation of DNA replication. More recent studies have shown that MCM proteins also function in replication elongation, probably as a DNA helicase. This is consistent with structural analysis showing that the proteins interact together in a heterohexameric ling. However, MCMs are strikingly abundant and far exceed the stoichiometry of replication origins; they are widely distributed on unreplicated chromatin. Analysis of mcm mutant phenotypes and interactions with other factors have now implicated the MCM proteins in other chromosome transactions including damage response, transcription, and chromatin structure. These experiments indicate that the MCMs are central players in many aspects of genome stability.
引用
收藏
页码:109 / +
页数:24
相关论文
共 363 条
[1]   Structure, expression, and chromosomal localization of the human gene encoding a germinal center-associated nuclear protein (GANP) that associates with MCM3 involved in the initiation of DNA replication [J].
Abe, E ;
Kuwahara, K ;
Yoshida, M ;
Suzuki, M ;
Terasaki, H ;
Matsuo, Y ;
Takahashi, E ;
Sakaguchi, N .
GENE, 2000, 255 (02) :219-227
[2]   A globular complex formation by Nda1 and the other five members of the MCM protein family in fission yeast [J].
Adachi, Y ;
Usukura, J ;
Yanagida, M .
GENES TO CELLS, 1997, 2 (07) :467-479
[3]   Minichromosome maintenance (MCM) proteins may be pre-cancer markers [J].
Alison, MR ;
Hunt, T ;
Forbes, SJ .
GUT, 2002, 50 (03) :290-291
[4]   Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication [J].
Aparicio, OM ;
Stout, AM ;
Bell, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9130-9135
[5]   Components and dynamics of DNA replication complexes in S-cerevisiae: Redistribution of MCM proteins and Cdc45p during S phase [J].
Aparicio, OM ;
Weinstein, DM ;
Bell, SP .
CELL, 1997, 91 (01) :59-69
[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]   Cdk2-dependent and -independent pathways in E2F-mediated S phase induction [J].
Arata, Y ;
Fujita, M ;
Ohtani, K ;
Kijima, S ;
Kato, JY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6337-6345
[8]   A ROLE FOR CDC7 IN REPRESSION OF TRANSCRIPTION AT THE SILENT MATING-TYPE LOCUS HMR IN SACCHAROMYCES-CEREVISIAE [J].
AXELROD, A ;
RINE, J .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :1080-1091
[9]   Hsk1-Dfp1 is required for heterochromatin-mediated cohesion at centromeres [J].
Bailis, JM ;
Bernard, P ;
Antonelli, R ;
Allshire, RC ;
Forsburg, SL .
NATURE CELL BIOLOGY, 2003, 5 (12) :1111-1116
[10]   It's All in the Timing Linking S Phase to Chromatin Structure and Chromosome Dynamics [J].
Bailis, Julie M. ;
Forsburg, Susan L. .
CELL CYCLE, 2003, 2 (04) :303-306