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Microbiology (Reading) ; 163(9): 1329-1342, 2017 09.
Artículo en Inglés | MEDLINE | ID: mdl-28100304

RESUMEN

In Entamoeba histolytica, iron modulates virulence and gene expression via unknown regulatory mechanisms. The existence of a posttranscriptional iron regulatory system parallel with the iron-responsive element (IRE)/iron regulatory protein (IRP) system in the protozoan Trichomonas vaginalis has recently been reported. Due to their evolutionary closeness and the importance of iron for growth and virulence in these protozoa, we hypothesized the existence of an IRE/IRP-like mechanism in E. histolytica. To determine the presence of IRE-like elements in some mRNAs from this parasite, we performed in silico analyses of the 5'- and 3'-UTRs of mRNAs encoding virulence factors and cytoskeleton, ribosomal and metabolism proteins. The Zuker mfold software predicted IRE-like secondary structures in 52 of the 135 mRNAs analysed. However, only nine structures shared sequence similarity with the apical loop sequence (CAGUGN) of the previously reported human IRE-ferritin, whereas the GUU/UUG protozoan-specific motif was detected in 23 stem-loop structures. A new motif, AUU/AUUU, was also observed in 23 structures, suggesting the possible existence of an amoeba-specific motif. Additionally, cross-linking and RNA electrophoretic mobility shift assays showed specific RNA-protein interactions, using as a model two amoebic IRE-like elements from iron-regulated mRNAs and HeLa, T. vaginalis and E. histolytica cytoplasmic proteins. Our data suggest the presence of a posttranscriptional iron regulatory IRE/IRP-like mechanism in E. histolytica.


Asunto(s)
Entamoeba histolytica/genética , Entamoeba histolytica/metabolismo , Regulación de la Expresión Génica , Hierro/metabolismo , Elementos de Respuesta , Células Cultivadas , Entamebiasis/metabolismo , Entamebiasis/parasitología , Células HeLa , Interacciones Huésped-Parásitos , Humanos , Secuencias Invertidas Repetidas , Conformación de Ácido Nucleico , Unión Proteica , ARN Mensajero/química , ARN Mensajero/genética
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