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Journal of Bacteriology, March 1999, p. 1562-1568, Vol. 181, No. 5
Department of Plant Pathology, Cornell
University, Ithaca, New York 14853
Received 2 October 1998/Accepted 11 December 1998
Streptomycetes are common soil inhabitants, yet few described
species are plant pathogens. While the
pathogenicity mechanisms remain unclear, previous work
identified a gene, nec1, which encodes a putative
pathogenicity or virulence factor. nec1 and
a neighboring transposase pseudogene, ORFtnp, are conserved
among unrelated plant pathogens and absent from nonpathogens. The
atypical GC content of nec1 suggests that it was acquired
through horizontal transfer events. Our investigation of the genetic
organization of regions adjacent to the 3' end of nec1 in
Streptomyces scabies 84.34 identified a new insertion
sequence (IS) element, IS1629, with homology to other IS
elements from prokaryotic animal pathogens. IS1629 is 1,462 bp with 26-bp terminal inverted repeats and encodes a putative
431-amino-acid (aa) transposase. Transposition of
IS1629 generates a 10-bp target site duplication.
A 77-nucleotide (nt) sequence encompassing the start codon and upstream
region of the transposase was identified which could function in the
posttranscritpional regulation of transposase synthesis. A functional
copy of IS1629 from S. turgidiscabies 94.09 (Hi-C-13) was selected in
the transposon trap pCZA126, through its insertion into the
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Characterization of an Insertion Sequence Element
Associated with Genetically Diverse Plant Pathogenic
Streptomyces spp.
cI857 repressor. IS1629 is present in multiple
copies in some S. scabies strains and is present in
all S. acidiscabies and S. turgidiscabies strains examined. A second copy of
IS1629 was identified between ORFtnp and
nec1 in S. acidiscabies
strains. The diversity of IS1629 hybridization profiles was
greatest within S. scabies. IS1629 was
absent from the 27 nonpathogenic Streptomyces strains
tested. The genetic organization and nucleotide sequence of the
nec1-IS1629 region was conserved and identical
among representatives of S. acidiscabies and S. turgidiscabies. These findings
support our current model for the unidirectional transfer of
the ORFtnp-nec1-IS1629 locus from
IS1629-containing S. scabies (type II) to
S. acidiscabies and S. turgidiscabies.
*
Corresponding author. Mailing address: Department of
Plant Pathology, Cornell University, Ithaca, NY 14853. Phone: (607)
255-7831. Fax: (607) 255-4471. E-mail: rl21{at}cornell.edu.
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