name: Actinobacteriophage_706 version: 1 date: 2016-02-25 owner: name: Graham Hatfull email: gfh@pitt.edu url: https://www.biology.pitt.edu/person/graham-hatfull description: > This database contains the 706 manually annotated Actinobacteriophages analyzed in Dedrick et al 2016. publications: 1: doi: 10.1111/mmi.13414 pmid: 27146086 title: > Function, expression, specificity, diversity, and incompatibility of actinobacteriophage parABS systems authors: > Rebekah M Dedrick, Travis N Mavrich, Wei L Ng, Juan C Cervantes Reyes, Matthew R Olm, Rachael E Rush, Deborah Jacobs-Sera, Daniel A Russel, Graham F Hatfull abstract: > More than 180 individual phages infecting hosts in the phylum Actinobacteria have been sequenced and grouped into Cluster A because of their similar overall nucleotide sequences and genome architectures. These Cluster A phages are either temperate or derivatives of temperate parents, and most have an integration cassette near the center of the genome containing an integrase gene and attP. However, about 20% of the phages lack an integration cassette, which is replaced by a 1.4 kbp segment with predicted partitioning functions, including plasmid-like parA and parB genes. Phage RedRock forms stable lysogens in Mycobacterium smegmatis in which the prophage replicates at 2.4 copies/chromosome and the partitioning system confers prophage maintenance. The parAB genes are expressed upon RedRock infection of M. smegmatis, but are down-regulated once lysogeny is established by binding of RedRock ParB to parS-L, one of two centromere-like sites flanking the parAB genes. The RedRock parS-L and parS-R sites are composed of eight directly repeated copies of an 8 bp motif that is recognized by ParB. The actinobacteriophage parABS cassettes span considerable sequence diversity and specificity, providing a suite of tools for use in mycobacterial genetics. resources: ~