Duigou Stéphane, Yamaichi Yoshiharu, Waldor Matthew K
Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School and Howard Hughes Medical Institute, 181 Longwood Avenue, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10577-82. doi: 10.1073/pnas.0803904105. Epub 2008 Jul 22.
Vibrio cholerae, the agent of cholera, has two circular chromosomes. In bacteria that contain a single chromosome, initiation of chromosome DNA replication is mediated by DnaA, a AAA+ ATPase that unwinds the origin of replication. There is little knowledge regarding initiation of chromosome replication in bacteria with more than one chromosome. Here, we purified V. cholerae DnaA and RctB, which have been implicated in the replication of V. cholerae chromosome II, and characterized their activities in vitro. We found that RctB has origin-specific unwinding activity and can melt the origin of chromosome II (oriCIIvc) but not the origin of chromosome I (oriCIvc); conversely, DnaA promoted the unwinding of oriCIvc and not oriCIIvc. The activity of DnaA and several plasmid initiator proteins is stimulated by ATP binding. We found that RctB bound and hydrolyzed ATP even though RctB lacks any apparent ATP-binding motifs. However, we unexpectedly found that ATP inhibited the oriCIIvc binding activity of RctB, suggesting that the ATP-bound form of RctB cannot initiate replication of chromosome II. Supporting this idea, we identified an RctB mutant that does not bind ATP and found that expression of this ATP-blind RctB mutant in V. cholerae leads to significant overinitiation of chromosome II and marked inhibition of V. cholerae growth. These observations suggest that the rules that license the replication of the two V. cholerae chromosomes differ.
霍乱弧菌是霍乱的病原体,有两条环状染色体。在含有单条染色体的细菌中,染色体DNA复制的起始由DnaA介导,DnaA是一种能解开复制起点的AAA + ATP酶。对于具有多条染色体的细菌中染色体复制的起始了解甚少。在这里,我们纯化了与霍乱弧菌染色体II复制有关的霍乱弧菌DnaA和RctB,并在体外对它们的活性进行了表征。我们发现RctB具有特定于起点的解旋活性,能解开染色体II的起点(oriCIIvc),但不能解开染色体I的起点(oriCIvc);相反,DnaA促进oriCIvc的解旋,而不是oriCIIvc的解旋。DnaA和几种质粒起始蛋白的活性受ATP结合的刺激。我们发现RctB能结合并水解ATP,尽管RctB缺乏任何明显的ATP结合基序。然而,我们意外地发现ATP抑制了RctB与oriCIIvc的结合活性,这表明ATP结合形式的RctB不能启动染色体II的复制。支持这一观点的是,我们鉴定出一个不结合ATP的RctB突变体,并发现该ATP不敏感的RctB突变体在霍乱弧菌中的表达导致染色体II的过度起始,并显著抑制霍乱弧菌的生长。这些观察结果表明,许可霍乱弧菌两条染色体复制的规则是不同的。