Terzano S, Christian R, Espinoza F H, Calendar R, Dehò G, Ghisotti D
Dipartimento di Genetica e di Biologia dei Microrganismi, Università di Milano, Italy.
J Bacteriol. 1994 Oct;176(19):6059-65. doi: 10.1128/jb.176.19.6059-6065.1994.
Bacteriophage P4 replication may result in either a lytic cycle or plasmid maintenance, depending on the presence or absence, respectively, of helper phase P2 genome. Bacteriophage P4 DNA replication depends on the product of gene alpha, which has origin recognition, primase, and helicase activities. An open reading frame with the coding capacity for a protein of 106 amino acids (orf106) is located upstream of the alpha gene. Genes orf106 and alpha are transcriptionally coregulated. Three amber mutations and an internal deletion (del51) were introduced into orf106. All of the amber mutations exhibited a polar effect on transcription of the downstream alpha gene. The P4 del51 mutant was slightly defective in lytic growth and could not be propagated in the plasmid state. In this latter condition, P4 DNA overreplication was observed. Overexpression of Orf106 severely inhibited P4 DNA replication, preventing P4 lytic growth and plasmid maintenance. The inhibitory effect of Orf106 on P4 replication was not observed when both orf106 and alpha were overexpressed. We suggest that orf106 is involved in P4 replication and that a balanced expression of orf106 relative to alpha may be necessary for proper P4 DNA replication. In particular, orf106 appears to be essential for the control of P4 genome replication in the plasmid state. We propose that orf106 be named cnr, for copy number regulation.
噬菌体P4的复制可能导致裂解循环或质粒维持,这分别取决于辅助噬菌体P2基因组的存在与否。噬菌体P4的DNA复制依赖于α基因的产物,该产物具有起始识别、引发酶和解旋酶活性。一个编码106个氨基酸的蛋白质的开放阅读框(orf106)位于α基因的上游。orf106和α基因在转录上是共调控的。三个琥珀突变和一个内部缺失(del51)被引入到orf106中。所有的琥珀突变对下游α基因的转录都表现出极性效应。P4 del51突变体在裂解生长方面略有缺陷,并且不能以质粒状态繁殖。在后一种情况下,观察到P4 DNA过度复制。Orf106的过表达严重抑制了P4 DNA的复制,阻止了P4的裂解生长和质粒维持。当orf106和α基因都过表达时,未观察到Orf106对P4复制的抑制作用。我们认为orf106参与了P4的复制,并且相对于α基因,orf106的平衡表达可能是P4 DNA正确复制所必需的。特别是,orf106似乎对于控制质粒状态下的P4基因组复制至关重要。我们建议将orf106命名为cnr,即拷贝数调节。