Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9442976 | Experimental Parasitology | 2005 | 6 Pages |
Abstract
The Entamoeba histolytica Ehcp112 and Ehadh112 genes that encode the EhCPADH complex are separated by a non-coding 188Â pb region. Their proximity suggests a coordinated expression regulation for both genes. Here, we studied the structure and function of 996Â bp (p996CAT) upstream the ATG start codon of the Ehadh112 gene. The p996CAT plasmid drove CAT transcription with a 78% of the activity showed by actin promoter. Deletion of 330Â bp at the 5â² end of p966CAT to produce the p776CAT plasmid, decreased activity to 40% in relation to actin promoter and to 50% of p996CAT, suggesting the presence of a silencer in this region. Interestingly, deletion of other 297Â bp to the p776CAT to generate the p469CAT plasmid, augmented activity in 2.5-fold compared with p776CAT construction, showing the presence of a proximal enhancer promoter. Transcription initiation sites (â69 and â150Â bp), TATA like box, GAAC, and Inr elements, as well as putative DNA binding motifs, were mapped in the â1 to â469Â bp core promoter region.
Keywords
Related Topics
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Immunology and Microbiology
Parasitology
Authors
E. Azuara-Liceaga, E. Flores-Soto, C. López-Camarillo, E. Orozco,