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Nucleic Acids Res. 2013 Mar 1;41(5):3094-103. doi: 10.1093/nar/gkt018. Epub 2013 Jan 23.

Insight into centromere-binding properties of ParB proteins: a secondary binding motif is essential for bacterial genome maintenance.

Author information

1
Laboratoire de Microbiologie et Génétique Moléculaires, Centre National de la Recherche Scientifique, F-31000 Toulouse, France.

Abstract

ParB proteins are one of the three essential components of partition systems that actively segregate bacterial chromosomes and plasmids. In binding to centromere sequences, ParB assembles as nucleoprotein structures called partition complexes. These assemblies are the substrates for the partitioning process that ensures DNA molecules are segregated to both sides of the cell. We recently identified the sopC centromere nucleotides required for binding to the ParB homologue of plasmid F, SopB. This analysis also suggested a role in sopC binding for an arginine residue, R219, located outside the helix-turn-helix (HTH) DNA-binding motif previously shown to be the only determinant for sopC-specific binding. Here, we demonstrated that the R219 residue is critical for SopB binding to sopC during partition. Mutating R219 to alanine or lysine abolished partition by preventing partition complex assembly. Thus, specificity of SopB binding relies on two distinct motifs, an HTH and an arginine residue, which define a split DNA-binding domain larger than previously thought. Bioinformatic analysis over a broad range of chromosomal ParBs generalized our findings with the identification of a non-HTH positively charged residue essential for partition and centromere binding, present in a newly identified highly conserved motif. We propose that ParB proteins possess two DNA-binding motifs that form an extended centromere-binding domain, providing high specificity.

PMID:
23345617
PMCID:
PMC3597684
DOI:
10.1093/nar/gkt018
[Indexed for MEDLINE]
Free PMC Article

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