Affiliation:
1. Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany
Abstract
ABSTRACT
Transcriptional silencing by
trans
inactivation can contribute to the regulation of gene expression in eukaryotic cells. In the human intestinal protozoan parasite
Entamoeba histolytica
,
trans
inactivation of the amoebapore-A gene (
AP-A
) was recently achieved by episomal transfection of
E. histolytica
trophozoites with the plasmid psAP1. The mechanism of
AP-A trans
inactivation is largely unknown, though it was suggested that a partial short interspersed transposable element (SINE) is required. By systematic assessment of various
E. histolytica
isolates transfected with psAP1 derivates,
trans
inactivation of
AP-A
was restricted to the strain HM-1:IMSS (2411) but could not be achieved in other standard laboratory strains. Importantly, sequences of an
E. histolytica
tRNA array that were located on psAP1 in close proximity to the
AP-A
upstream region and comprising the glutamic acid (TTC) (E) and tyrosine (GTA) (Y) tRNA genes were indispensable for
AP-A
silencing. In contrast to the case described in previous reports, SINE was not required for
AP-A trans
inactivation.
AP-A
expression could be regained in silenced cells by episomal transfection under the control of a heterologous
E. histolytica
promoter, opening a way toward future silencing of individual genes of interest in
E. histolytica
. Our results indicate that tRNA gene-mediated silencing is not restricted to
Saccharomyces cerevisiae
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
10 articles.
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