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Replication of G Quadruplex DNA
被引:113
|作者:
Lerner, Leticia Koch
[1
]
Sale, Julian E.
[1
]
机构:
[1] MRC Lab Mol Biol, Francis Crick Ave, Cambridge CB2 0QH, England
来源:
关键词:
G quadruplex;
DNA replication;
DNA helicases;
DNA secondary structure;
WERNER-SYNDROME HELICASE;
EUKARYOTIC CMG HELICASE;
DOUBLE-STRANDED DNA;
ATAXIA GAA REPEATS;
PROTEIN-A;
TELOMERIC DNA;
SECONDARY STRUCTURES;
GENE-PRODUCT;
BIOCHEMICAL-CHARACTERIZATION;
TETRAMOLECULAR QUADRUPLEX;
D O I:
10.3390/genes10020095
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
A cursory look at any textbook image of DNA replication might suggest that the complex machine that is the replisome runs smoothly along the chromosomal DNA. However, many DNA sequences can adopt non-B form secondary structures and these have the potential to impede progression of the replisome. A picture is emerging in which the maintenance of processive DNA replication requires the action of a significant number of additional proteins beyond the core replisome to resolve secondary structures in the DNA template. By ensuring that DNA synthesis remains closely coupled to DNA unwinding by the replicative helicase, these factors prevent impediments to the replisome from causing genetic and epigenetic instability. This review considers the circumstances in which DNA forms secondary structures, the potential responses of the eukaryotic replisome to these impediments in the light of recent advances in our understanding of its structure and operation and the mechanisms cells deploy to remove secondary structure from the DNA. To illustrate the principles involved, we focus on one of the best understood DNA secondary structures, G quadruplexes (G4s), and on the helicases that promote their resolution.
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