Universite de Versailles Saint-Quentin, 45 Avenue des Etats-Unis, Versailles 78000, France.
Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, Gif-sur-Yvette 91198, France.
Nat Commun. 2016 Nov 10;7:13271. doi: 10.1038/ncomms13271.
Delivery of the replicative helicase onto DNA is an essential step in the initiation of replication. In bacteria, DnaC (in Escherichia coli) and DnaI (in Bacillus subtilis) are representative of the two known mechanisms that assist the replicative helicase at this stage. Here, we establish that these two strategies cannot be regarded as prototypical of the bacterial domain since dnaC and dnaI (dna[CI]) are present in only a few bacterial phyla. We show that dna[CI] was domesticated at least seven times through evolution in bacteria and at the expense of one gene, which we rename dciA (dna[CI] antecedent), suggesting that DciA and Dna[CI] share a common function. We validate this hypothesis by establishing in Pseudomonas aeruginosa that DciA possesses the attributes of the replicative helicase-operating proteins associated with replication initiation.
将复制解旋酶递送到 DNA 上是复制起始的一个关键步骤。在细菌中,DnaC(大肠杆菌)和 DnaI(枯草芽孢杆菌)是协助复制解旋酶在该阶段发挥作用的两种已知机制的代表。在这里,我们确定这两种策略不能被视为细菌域的典型代表,因为 dnaC 和 dnaI(dna[CI])仅存在于少数细菌门中。我们表明,dna[CI] 在细菌中至少经过了七次进化的驯化,牺牲了一个基因,我们将其重新命名为 dciA(dna[CI] 前体),表明 DciA 和 dna[CI] 具有共同的功能。我们通过在铜绿假单胞菌中证实了这一假设,即 DciA 具有与复制起始相关的复制解旋酶作用蛋白的属性。