Abstract

The genomes of the spirochetes of the genus Borrelia are unique among prokaryotes; all member species possess a linear chromosome as well as linear plasmids terminated by covalently closed DNA hairpins, or hairpin telomeres. The usual “end-replication problem” for linear replicons is overcome by the hairpin telomeres presenting to the cellular replication machinery an uninterrupted DNA chain. DNA replication initiates internally and proceeds bidirectionally. Replication through the hairpin turnaround at the telomeres produces replication intermediates that possess inverted repeat replicated telomere junctions, which act as the substrates for a specialized DNA breakage and reunion enzyme referred to as a telomere resolvase. The telomere resolvase converts each replicated telomere into two hairpin telomeres, thereby liberating linear daughter chromosomes from the replicated intermediates. The telomere resolution reaction has mechanistic similarities to those catalysed by type IB topoisomerases and tyrosine recombinases. Details of the replication and telomere resolution processes have been revealed by recent molecular biology and biochemical studies in Borrelia burgdorferi, the causative agent of Lyme disease.

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