共 68 条
Insights into the Initiation of Eukaryotic DNA Replication
被引:17
作者:
Bruck, Irina
[1
]
Perez-Arnaiz, Patricia
[1
]
Colbert, Max K.
[1
]
Kaplan, Daniel L.
[1
]
机构:
[1] Florida State Univ, Coll Med, Dept Biomed Sci, Tallahassee, FL 32306 USA
来源:
基金:
美国国家科学基金会;
关键词:
cancer;
DNA replication;
eukaryotic;
helicase;
initiation;
S-PHASE;
SACCHAROMYCES-CEREVISIAE;
FORK HELICASE;
BUDDING YEAST;
POLYMERASE-ALPHA;
CHROMATIN BINDING;
MCM2-7;
HELICASE;
MCM10;
PLAYS;
HUMAN-CELLS;
ORIGIN DNA;
D O I:
10.1080/19491034.2015.1115938
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The initiation of DNA replication is a highly regulated event in eukaryotic cells to ensure that the entire genome is copied once and only once during S phase. The primary target of cellular regulation of eukaryotic DNA replication initiation is the assembly and activation of the replication fork helicase, the 11-subunit assembly that unwinds DNA at a replication fork. The replication fork helicase, called CMG for Cdc45-Mcm2-7, and GINS, assembles in S phase from the constituent Cdc45, Mcm2-7, and GINS proteins. The assembly and activation of the CMG replication fork helicase during S phase is governed by 2 S-phase specific kinases, CDK and DDK. CDK stimulates the interaction between Sld2, Sld3, and Dpb11, 3 initiation factors that are each required for the initiation of DNA replication. DDK, on the other hand, phosphorylates the Mcm2, Mcm4, and Mcm6 subunits of the Mcm2-7 complex. Sld3 recruits Cdc45 to Mcm2-7 in a manner that depends on DDK, and recent work suggests that Sld3 binds directly to Mcm2-7 and also to single-stranded DNA. Furthermore, recent work demonstrates that Sld3 and its human homolog Treslin substantially stimulate DDK phosphorylation of Mcm2. These data suggest that the initiation factor Sld3/Treslin coordinates the assembly and activation of the eukaryotic replication fork helicase by recruiting Cdc45 to Mcm2-7, stimulating DDK phosphorylation of Mcm2, and binding directly to single-stranded DNA as the origin is melted.
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页码:449 / 454
页数:6
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