oriD structure controls RepD initiation during rolling-circle replication

被引:6
|
作者
Toleikis, Algirdas [1 ,2 ]
Webb, Martin R. [1 ]
Molloy, Justin E. [1 ]
机构
[1] Francis Crick Inst, 1 Midland Rd, London NW1 1AT, England
[2] Univ Warwick, WMS Cell & Dev Biol, Coventry CV4 7AL, W Midlands, England
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
英国惠康基金; 英国医学研究理事会;
关键词
PLASMID REPLICATION; PT181; PLASMID; CRUCIFORM EXTRUSION; DNA; PROTEIN; ORIGIN; SPECIFICITY; PCRA; ELASTICITY;
D O I
10.1038/s41598-017-18817-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bacterial antibiotic resistance is often carried by circular DNA plasmids that are copied separately from the genomic DNA and can be passed to other bacteria, spreading the resistance. The chloramphenicol-resistance plasmid pC221 from Staphylococcus aureus is duplicated by a process called asymmetric rolling circle replication. It is not fully understood how the replication process is regulated but its initiation requires a plasmid-encoded protein called RepD that nicks one strand of the parent plasmid at the double-stranded origin of replication (oriD). Using magnetic tweezers to control the DNA linking number we found RepD nicking occurred only when DNA was negatively supercoiled and that binding of a non-nicking mutant (RepDY188F) stabilized secondary structure formation at oriD. Quenched-flow experiments showed the inverted complementary repeat sequence, ICRII, within oriD was most important for rapid nicking of intact plasmids. Our results show that cruciform formation at oriD is an important control for initiation of plasmid replication.
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页数:12
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