Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9442977 | Experimental Parasitology | 2005 | 6 Pages |
Abstract
Ehcp112 encodes the Entamoeba histolytica EhCP112 cysteine protease that is part of the EhCPADH complex. By in silico analysis we identified putative transcription factor-binding sites along 837Â bp upstream the Ehcp112 gene ATG codon. A TATA-like motif (TATATAAA) was located at â36 to â29Â bp, a GAAC box (GAACC) was found at â10 to â14Â bp and an Inr sequence (TTCAAC) at â8 to â2Â bp. These tripartite promoter elements are in non-canonical positions, downstream the transcription initiation site (â280Â bp). We cloned four Ehcp112 promoter fragments in pBSCAT-ACT plasmid to obtain pI (355Â bp), pII (681Â bp), pIII (833Â bp), and pIV (554Â bp) constructs. In transfected trophozoites, only pIII drove CAT activity with 44% efficiency in relation to actin promoter activity. Our results showed the presence of a distal and weak promoter in the Ehcp112 gene. The active DNA region is inside the open reading frame of the Ehrab B gene, suggesting that expression of both genes could be coordinately regulated.
Keywords
Related Topics
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Immunology and Microbiology
Parasitology
Authors
E. Flores-Soto, E. Azuara-Liceaga, C. López-Camarillo, E. Orozco,