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DNA Replication through G-Quadruplex Motifs Is Promoted by the Saccharomyces cerevisiae Pif1 DNA Helicase
被引:451
|作者:
Paeschke, Katrin
[1
]
Capra, John A.
[2
]
Zakian, Virginia A.
[1
]
机构:
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Univ Calif San Francisco, Gladstone Inst, San Francisco, CA 94158 USA
来源:
关键词:
FALSE DISCOVERY RATE;
TELOMERE ELONGATION;
FORK PROGRESSION;
YEAST;
RRM3P;
INSTABILITY;
SEQUENCES;
PROTEIN;
GENES;
PAUSE;
D O I:
10.1016/j.cell.2011.04.015
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:
G-quadruplex (G4) DNA structures are extremely stable four-stranded secondary structures held together by noncanonical G-G base pairs. Genome-wide chromatin immunoprecipitation was used to determine the in vivo binding sites of the multifunctional Saccharomyces cerevisiae Pif1 DNA helicase, a potent unwinder of G4 structures in vitro. G4 motifs were a significant subset of the high-confidence Pif1-binding sites. Replication slowed in the vicinity of these motifs, and they were prone to breakage in Pif1-deficient cells, whereas non-G4 Pif1-binding sites did not show this behavior. Introducing many copies of G4 motifs caused slow growth in replication-stressed Pif1-deficient cells, which was relieved by spontaneous mutations that eliminated their ability to form G4 structures, bind Pif1, slow DNA replication, and stimulate DNA breakage. These data suggest that G4 structures form in vivo and that they are resolved by Pif1 to prevent replication fork stalling and DNA breakage.
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页码:678 / 691
页数:14
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