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Genetic organization of the psbAD region in phages infecting marine Synechococcus strains
Author(s) -
Andrew Millard,
Martha R. J. Clokie,
David A. Shub,
Nicholas H. Mann
Publication year - 2004
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0401478101
Subject(s) - biology , prochlorococcus , horizontal gene transfer , gene , genetics , synechococcus , bacteriophage , genome , lineage (genetic) , phylogenetic tree , evolutionary biology , cyanobacteria , bacteria , escherichia coli
The discovery of the genespsbA andpsbD , encoding the D1 and D2 core components of the photosynthetic reaction center PSII (photosystem II), in the genome of the bacteriophage S-PM2 (a cyanomyovirus) that infects marine cyanobacteria begs the question as to how these genes were acquired. In an attempt to answer this question, it was established that the occurrence of the genes is widespread among marine cyanomyovirus isolates and may even extend to podoviruses. The phagepsbA genes fall into a clade that includes thepsbA genes from their potentialSynechococcus andProchlorococcus hosts, and thus, this phylogenetic analysis provides evidence to support the idea of the acquisition of these genes by horizontal gene transfer from their cyanobacterial hosts. However, the phagepsbA genes form distinct subclades within this lineage, which suggests that their acquisition was not very recent. ThepsbA genes of two phages contain identical 212-bp insertions that exhibit all of the canonical structural features of a group I self-splicing intron. The different patterns of genetic organization of thepsbAD region are consistent with the idea that thepsbA andpsbD genes were acquired more than once by cyanomyoviruses and that their horizontal transfer between phages via a common phage gene pool, as part of mobile genetic modules, may be a continuing process. In addition, genes were discovered encoding a high-light inducible protein and a putative key enzyme of dark metabolism, transaldolase, extending the areas of host-cell metabolism that may be affected by phage infection.

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