López-Camarillo César, Luna-Arias Juan Pedro, Marchat Laurence A, Orozco Esther
Programa de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatia del Instituto Politécnico Nacional, CP 07300, México, Distrito Federal.
J Biol Chem. 2003 Mar 28;278(13):11273-80. doi: 10.1074/jbc.M211757200. Epub 2003 Jan 28.
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 microM and to 7.8 h with 225 microM 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 microM emetine exhibited an extra polyadenylation site at 19 nt. The 3'-untranslated region sequence is AU-rich and has putative consensus sequences for RNA-binding 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 microM 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.
溶组织内阿米巴的多药耐药(MDR)表型的特征是,在高药物浓度下生长的滋养体中EhPgp5基因过度表达。在此,我们使用放线菌素D评估了EhPgp5 mRNA稳定性对MDR的作用。未用吐根碱培养的滋养体中的EhPgp5 mRNA半衰期为2.1小时,在用90微摩尔培养的细胞中增至3.1小时,在用225微摩尔吐根碱培养的细胞中增至7.8小时。在EhPgp5 mRNA 3'非翻译区的118、156和189个核苷酸(nt)位置检测到多聚腺苷酸化位点。有趣的是,用225微摩尔吐根碱培养的滋养体在19 nt处表现出一个额外的多聚腺苷酸化位点。3'非翻译区序列富含AU,并且具有RNA结合蛋白的推定共有序列。我们在一个包含多嘧啶序列(142 - 159 nt)和细胞质多聚腺苷酸化元件(146 - 154 nt)的区域检测到一种RNA - 蛋白质复合物。在用225微摩尔吐根碱培养的滋养体中观察到EhPgp5 mRNA的多聚(A)尾更长。吐根碱应激可能影响参与mRNA周转的因子,包括多聚腺苷酸化/去腺苷酸化蛋白,这可能导致EhPgp5 mRNA半衰期和多聚(A)尾长度的变化。提供了关于参与溶组织内阿米巴MDR表型机制的新证据。