Affiliation:
1. Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Abstract
ABSTRACT
Transcriptional silencing of the gene coding for amoebapore A (AP-A) was observed when trophozoites of
Entamoeba histolytica
were transfected with a hybrid plasmid construct containing the
ap-a
gene flanked by the upstream and downstream segments of the original
Ehap-a
gene. Transfectants were totally devoid of
ap-a
transcript and AP-A protein. An identical silencing effect was observed upon transfection with a plasmid that contained only the 5′ upstream region of
ap-a
. Removal of the selecting antibiotic enabled the isolation of plasmidless clones, which retained in their progeny the silenced phenotype.
E. histolytica
cells were able to overexpress
ap-a
when transfected with a plasmid containing the gene flanked by the 5′ and 3′ regions of the
EhRP-L21
gene. This plasmid, however, could not express
ap-a
in the retransfected, cloned trophozoites lacking AP-A. This is the first report of gene silencing in
E. histolytica
, and the mechanism appears to belong to transcriptional gene silencing and not to posttranscriptional gene silencing. This conclusion is based on the following results: (i) silencing was achieved by transfection of homologous 5′ flanking sequences (470 bp of the
Ehap-a
gene), (ii) transcription initiation of
Ehap-a
was found to be blocked, and (iii) short double-stranded RNA fragments of the
ap-a
coding and noncoding sequences were not detected. Trophozoites lacking AP-A are nonpathogenic and impaired in their bacteriolytic capability.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
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