Abstract

Agrobacterium tumefaciens C58, the pathogenic bacteria that causes crown gall disease in plants, harbors one circular and one linear chromosome and two circular plasmids. The telomeres of its unusual linear chromosome are covalently closed hairpins. The circular and linear chromosomes co-segregate and are stably maintained in the organism. We have determined the sequence of the two ends of the linear chromosome thus completing the previously published genome sequence of A. tumefaciens C58. We found that the telomeres carry nearly identical 25-bp sequences at the hairpin ends that are related by dyad symmetry. We further showed that its Atu2523 gene encodes a protelomerase (resolvase) and that the purified enzyme can generate the linear chromosomal closed hairpin ends in a sequence-specific manner. Agrobacterium protelomerase, whose presence is apparently limited to biovar 1 strains, acts via a cleavage-and-religation mechanism by making a pair of transient staggered nicks invariably at 6-bp spacing as the reaction intermediate. The enzyme can be significantly shortened at both the N and C termini and still maintain its enzymatic activity. Although the full-length enzyme can uniquely bind to its product telomeres, the N-terminal truncations cannot. The target site can also be shortened from the native 50-bp inverted repeat to 26 bp; thus, the Agrobacterium hairpin-generating system represents the most compact activity of all hairpin linear chromosome- and plasmid-generating systems to date. The biochemical analyses of the protelomerase reactions further revealed that the tip of the hairpin telomere may be unusually polymorphically capable of accommodating any nucleotide.

Highlights

  • Protelomerase is an enzyme that generates closed hairpin ends in bacterial linear chromosomes

  • Telomeres of A. tumefaciens C58—The two published genomic sequences of A. tumefaciens C58 did not reach the telomeric ends of the linear chromosome, as the closed terminal fragments are expected to be absent from the collection of clones used in the sequencing projects

  • We set out to determine the terminal sequences of the linear chromosome using a different strategy by first identifying the two terminal fragments of the linear chromosome and opening the closed ends by single strand-specific nucleases, thereby making them accessible to ligation. This approach has been used successfully to determine the telomeres of the B. burgdorferi linear chromosome and some linear plasmids [1]

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Summary

Introduction

Protelomerase is an enzyme that generates closed hairpin ends in bacterial linear chromosomes. We further showed that its Atu2523 gene encodes a protelomerase (resolvase) and that the purified enzyme can generate the linear chromosomal closed hairpin ends in a sequencespecific manner.

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