The Escherichia coli Tus-Ter replication fork barrier causes site-specific DNA replication perturbation in yeast

被引:31
作者
Larsen, Nicolai B. [1 ]
Sass, Ehud [1 ,2 ]
Suski, Catherine [2 ]
Mankouri, Hocine W. [1 ,2 ]
Hickson, Ian D. [1 ,2 ]
机构
[1] Univ Copenhagen, Panum Inst, Dept Cellular & Mol Med, Nordea Ctr Healthy Aging, DK-2200 Copenhagen, Denmark
[2] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DS, England
基金
欧洲研究理事会;
关键词
S-PHASE CHECKPOINT; SACCHAROMYCES-CEREVISIAE; GENOME INSTABILITY; PROTEIN; RECOMBINATION; HELICASE; TERMINATION; RRM3P; PROGRESSION; MECHANISM;
D O I
10.1038/ncomms4574
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
Replication fork (RF) pausing occurs at both ` programmed' sites and non-physiological barriers (for example, DNA adducts). Programmed RF pausing is required for site-specific DNA replication termination in Escherichia coli, and this process requires the binding of the polar terminator protein, Tus, to specific DNA sequences called Ter. Here, we demonstrate that Tus-Ter modules also induce polar RF pausing when engineered into the Saccharomyces cerevisiae genome. This heterologous RF barrier is distinct from a number of previously characterized, protein-mediated, RF pause sites in yeast, as it is neither Tof1-dependent nor counteracted by the Rrm3 helicase. Although the yeast replisome can overcome RF pausing at Tus-Ter modules, this event triggers site-specific homologous recombination that requires the RecQ helicase, Sgs1, for its timely resolution. We propose that Tus-Ter can be utilized as a versatile, site-specific, heterologous DNA replication-perturbing system, with a variety of potential applications.
引用
收藏
页数:10
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