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Switching Protein-DNA Recognition Specificity by Single-Amino-Acid Substitutions in the P1 par Family of Plasmid Partition Elements

  1. Author:
    Dabrazhynetskaya, A.
    Brendler, T.
    Ji, X. H.
    Austin, S.
  2. Author Address

    Dabrazhynetskaya, Alena, Brendler, Therese, Austin, Stuart] NCI Frederick, CCR, Gene Regulat & Chromosome Biol Lab, Natl Canc Inst, Frederick, MD 21702 USA. [Ji, Xinhua] NCI Frederick, CCR, Macromol Crystallog Lab, Natl Canc Inst, Frederick, MD 21702 USA.
    1. Year: 2009
  1. Journal: Journal of Bacteriology
    1. 191
    2. 4
    3. Pages: 1126-1131
  2. Type of Article: Article
  1. Abstract:

    The P1, P7, and pMT1 par systems are members of the P1 par family of plasmid partition elements. Each has a ParA ATPase and a ParB protein that recognizes the parS partition site of its own plasmid type to promote the active segregation of the plasmid DNA to daughter cells. ParB contacts two parS motifs known as BoxA and BoxB, the latter of which determines species specificity. We found that the substitution of a single orthologous amino acid in ParB for that of a different species has major effects on the specificity of recognition. A single change in ParB can cause a complete switch in recognition specificity to that of another species or can abolish specificity. Specificity changes do not necessarily correlate with changes in the gross DNA binding properties of the protein. Molecular modeling suggests that species specificity is determined by the capacity to form a hydrogen bond between ParB residue 288 and the second base in the BoxB sequence. As changes in just one ParB residue and one BoxB base can alter species specificity, plasmids may use such simple changes to evolve new species rapidly.

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External Sources

  1. PMID: 19028896

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