EhPgp5 mRNA stability is a regulatory event in the entamoeba histolytica multidrug resistance phenotype

César López-Camarillo, Juan Pedro Luna-Arias, Laurence A. Marchat, Esther Orozco

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38 Scopus citations

Abstract

The multidrug resistance (MDR) phenotype in Entamoeba histolytica is characterized by the overexpression of the EhPgp5 gene in trophozoites grown in high drug concentrations. Here we evaluated the role of EhPgp5 mRNA stability on MDR using actinomycin D. EhPgp5 mRNA from trophozoites growing without emetine had a half-life of 2.1 h, which augmented to 3.1 h in cells cultured with 90 μm and to 7.8 h with 225 μm emetine. Polyadenylation sites were detected at 118-, 156-, and 189-nucleotide (nt) positions of the EhPgp5 mRNA 3′untranslated region. Interestingly, trophozoites grown with 225 μM emetine exhibited an extra polyadenylation site at 19 nt. The 3′-untranslated region sequence is AU-rich and has putative consensus sequences for RNAbinding proteins. We detected a RNA-protein complex in a region that contains a polypyrimidine tract (142-159 nt) and a cytoplasmic polyadenylation element (146-154 nt). A longer poly(A) tail in the EhPgp5 mRNA was seen in trophozoites grown with 225 μm emetine. Emetine stress may affect factors involved in mRNA turnover, including polyadenylation/deadenylation proteins, which could induce changes in the EhPgp5 mRNA half-life and poly(A) tail length. Novel evidence on mechanisms participating in E. histolytica MDR phenotype is provided.

Original languageEnglish
Pages (from-to)11273-11280
Number of pages8
JournalJournal of Biological Chemistry
Volume278
Issue number13
DOIs
StatePublished - 28 Mar 2003
Externally publishedYes

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