The small GTPase EhRabB of Entamoeba histolytica is differentially expressed during phagocytosis

被引:0
|
作者
Mario Hernandes-Alejandro
Mercedes Calixto-Gálvez
Israel López-Reyes
Andrés Salas-Casas
Javier Cázares-Ápatiga
Esther Orozco
Mario A. Rodríguez
机构
[1] Centro de Investigación y de Estudios Avanzados del IPN,Departamento de Infectómica y Patogénesis Molecular
[2] Instituto de Ciencia y Tecnología del Distrito Federal,Centro de Diagnóstico y Vigilancia Epidemiológica del Distrito Federal
[3] Universidad Autónoma del Estado de Hidalgo,Instituto de Ciencias de la Salud
来源
Parasitology Research | 2013年 / 112卷
关键词
Amebiasis; Entamoeba Histolytica; Chloramphenicol Acetyltransferase; Isopeptide Bond; Electrophoretic Mobility Shift Assay Experiment;
D O I
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中图分类号
学科分类号
摘要
It has been described that the pathogenicity of Entamoeba histolytica is influenced by environmental conditions and that transcription profile changes occur during invasion, suggesting that gene expression may be involved in the virulence of this parasite. However, the molecular mechanisms that are implicated in the control of gene expression in this microorganism are poorly understood. Here, we showed that the expression of the EhRabB protein, a small GTPase involved in phagocytosis, is modified through the interaction with red blood cells. By ELISA, Western blot, and immunofluorescence assays, we observed that the expression of EhRabB diminished after 5 min of the interaction of trophozoites with red blood cells, but protein level was recovered at subsequent times. In the EhRabB amino acid sequence, we found two lysine residues that could be target for ubiquitin modification and trigger the degradation of this GTPase at early times of phagocytosis. The analysis of the expression of the EhrabB mRNA showed that the interaction of trophozoites with red blood cells produces a drastic diminishing in its half-life. In addition, promoter assays using the chloramphenicol acetyltransferase reporter gene and electrophoretic mobility shift assays experiments showed that the URE1 motif located in the promoter region of EhrabB is involved in the expression regulation of this gene during phagocytosis. Moreover, the immunolocalization of the URE1-binding protein during phagocytosis indicated that the transcription of the EhrabB gene is determined, at least in part, by the translocation of this transcription factor to nuclei. These results suggested that the expression of particular genes of this parasite is controlled at several stages.
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页码:1631 / 1640
页数:9
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