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Vol 44(2010) N 2 p. 262-267;
A.V. Mardanov1, D. Lane2, N.V. Ravin1*

Sop Proteins Can Cause Transcriptional Silencing of Genes Located Close to the Centromere Sites of Linear Plasmid N15

1Bioengineering Center, Russian Academy of Sciences, Moscow, 117312, Russia
2Laboratoire de Microbiologie et Génétique Moléculaire, CNRS, Toulouse, France, 31062

*nravin@biengi.ac.ru
Received - 2009-07-21; Accepted - 2009-08-03

Stable inheritance of bacterial chromosomes and low copy number plasmids is ensured by accurate partitioning of replicated molecules between the daughter cells at division. Partitioning of the prophage of the temperate bacteriophage N15, which exists as a linear plasmid molecule with covalently closed ends, depends on the sop locus, comprising genes sopA and sopB, as well as four centromere sites in different regions of the N15 genome essential for replication and the control of lysogeny. We found that binding of SopB to the centromere could silence centromere-proximal promoters, presumably due to subsequent polymerization of SopB along the DNA. Close to the IR4 centromere site we identified a promoter, P59, which was able to drive the expression of phage late genes encoding structural proteins of virion. We found that, following binding to IR4, the N15 Sop proteins could induce repression of this promoter. The repression depended on SopB and was enhanced in the presence of SopA. Sop-dependent silencing of centromere-proximal promoters may control gene expression in phage N15, particularly preventing undesired expression of late genes in the N15 prophage. Thus, the phage N15 sop system not only ensures plasmid partitioning but is also involved in the genetic network controlling prophage replication and the maintenance of lysogeny.

bacteriophage N15, plasmid, sop/par genes, partitioning, promoter



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