Affiliation:
1. Division of Infectious Disease, Wadsworth Center, New York State Department of Health
2. Department of Biomedical Sciences, University at Albany, Albany, New York 12201
Abstract
ABSTRACT
Surprisingly little is known about the role of host factors in regulating transposition, despite the potentially deleterious rearrangements caused by the movement of transposons. An extensive mutant screen was therefore conducted to identify
Escherichia coli
host factors that regulate transposition. An
E. coli
mutant library was screened using a papillation assay that allows detection of IS
903
transposition events by the formation of blue papillae on a colony. Several host mutants were identified that exhibited a unique papillation pattern: a predominant ring of papillae just inside the edge of the colony, implying that transposition was triggered within these cells based on their spatial location within the colony. These mutants were found to be in
pur
genes, whose products are involved in the purine biosynthetic pathway. The transposition ring phenotype was also observed with Tn
552
, but not Tn
10
, establishing that this was not unique to IS
903
and that it was not an artifact of the assay. Further genetic analyses of purine biosynthetic mutants indicated that the ring of transposition was consistent with a GTP requirement for IS
903
and Tn
552
transposition. Together, our observations suggest that transposition occurs during late stages of colony growth and that transposition occurs inside the colony edge in response to both a gradient of exogenous purines across the colony and the developmental stage of the cells.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
16 articles.
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