Cloning and Partial Characterization of the Proteasome S4 ATPase from Plasmodium falciparum
Identifieur interne : 002684 ( Main/Exploration ); précédent : 002683; suivant : 002685Cloning and Partial Characterization of the Proteasome S4 ATPase from Plasmodium falciparum
Auteurs : Gabriela Certad [Canada] ; Abrahem Abrahem [Canada] ; Elias Georges [Canada]Source :
- Experimental Parasitology [ 0014-4894 ] ; 1999.
English descriptors
- Teeft :
- Abrahem, Academic press, Amino, Amino acid residues, Amino acid sequence, Amino acids, Annual review, Antimalarial drugs, Antisense primers, Atpase, Atpase homologue, Atpase subunits, Atpases, Biological chemistry, Cdna, Cdna encoding, Cell biology, Certad, Clone, Control antibody, Control cdna, Cytotoxicity assays, Degradation, Different clones, Encoding, Entamoeba histolytica, Eukaryotic cells, Experimental medicine, Experimental parasitology, Falciparum, High sequence identity, Immunoprecipitated, Immunoprecipitation, Irrelevant antibody, Lactacystin, Mammalian cells, Mcgill university, Molecular mass, Nitrocellulose membrane, Northern blot analysis, Open reading frame, Parasite, Parasitized, Parasitized rbcs, Partial characterization, Pathway, Pfs4, Pfs4 antiserum, Pfs4 cdna, Pfs4 cdna sequence, Pfs4 gene, Pfs4 proteins, Pfs4 sequence, Plasmodial proteins, Plasmodium, Plasmodium falciparum, Polypeptide, Positive control, Primer, Protease, Proteasome, Proteasome activities, Protein degradation, Reticulocyte lysate, Room temperature, Sequence identity, Similar molar concentrations, Southern blot analysis, Specific inhibitor, Specific interactions, Substrate specificity, Subunit, Ubiquinated proteins, Unique inserts.
Abstract
Abstract: Certad, G., Abrahem, A., and Georges, E. 1999. Cloning and Partial characterization of the proteasome S4 ATPase from Plasmodium falciparum. Experimental Parasitology93, 123–131. The ATP-ubiquitin-proteasome pathway mediates the nonlysosomal degradation of cytosolic proteins in eukaryotic cells. The activities of this pathway have been shown to regulate cell growth and differentiation through modulation of regulatory proteins. The proteasome is a large complex consisting of two multisubunit structures, the 20S and 19S(PA700) or P28 complexes, that combine to form the 26S particles. In this study, we describe the cloning of a cDNA encoding the proteasome subunit 4 ATPase homologue from Plasmodium falciparum (PFS4). Analysis of the PFS4 cDNA sequence shows an open reading frame encoding a deduced protein of 455 amino acids. Moreover, comparison of PFS4 cDNA sequence to that of genomic fragments encoding PFS4 showed identical sequences with no detectable introns. Database searches revealed a high sequence identity to those of rice, yeast, mouse, Drosophila, and human S4 ATPases. However, PFS4 contains two unique inserts of nine and seven amino acid residues in the N-terminal domain. Interestingly, only the rice S4 contains the latter (seven amino acids) insert with four identical amino acids. In vitro expression of the full-length cDNA encoding the PFS4, using a transcription-translation-coupled reticulocyte lysate, shows a 50-kDa [35S]methionine-labeled protein which was immunoprecipitated with PFS4 anti-peptide antiserum. Southern blot analysis of genomic DNA digests shows a single gene copy of PFS4 in P. falciparum. Of interest was the effect of the proteasome-specific natural product, lactacystin, on the growth of the parasite, with IC50 values of 0.6–0.92 μM. The latter IC50 values of lactacystin for different clones of P. falciparum are comparable to those obtained for mammalian cell lines (0.65 μM), suggesting the presence of a conserved proteasome complex. Moreover, lactacystin was equally toxic to drug-sensitive and resistant parasites.
Url:
DOI: 10.1006/expr.1999.4442
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: Certad, G., Abrahem, A., and Georges, E. 1999. Cloning and Partial characterization of the proteasome S4 ATPase from Plasmodium falciparum. Experimental Parasitology93, 123–131. The ATP-ubiquitin-proteasome pathway mediates the nonlysosomal degradation of cytosolic proteins in eukaryotic cells. The activities of this pathway have been shown to regulate cell growth and differentiation through modulation of regulatory proteins. The proteasome is a large complex consisting of two multisubunit structures, the 20S and 19S(PA700) or P28 complexes, that combine to form the 26S particles. In this study, we describe the cloning of a cDNA encoding the proteasome subunit 4 ATPase homologue from Plasmodium falciparum (PFS4). Analysis of the PFS4 cDNA sequence shows an open reading frame encoding a deduced protein of 455 amino acids. Moreover, comparison of PFS4 cDNA sequence to that of genomic fragments encoding PFS4 showed identical sequences with no detectable introns. Database searches revealed a high sequence identity to those of rice, yeast, mouse, Drosophila, and human S4 ATPases. However, PFS4 contains two unique inserts of nine and seven amino acid residues in the N-terminal domain. Interestingly, only the rice S4 contains the latter (seven amino acids) insert with four identical amino acids. In vitro expression of the full-length cDNA encoding the PFS4, using a transcription-translation-coupled reticulocyte lysate, shows a 50-kDa [35S]methionine-labeled protein which was immunoprecipitated with PFS4 anti-peptide antiserum. Southern blot analysis of genomic DNA digests shows a single gene copy of PFS4 in P. falciparum. Of interest was the effect of the proteasome-specific natural product, lactacystin, on the growth of the parasite, with IC50 values of 0.6–0.92 μM. The latter IC50 values of lactacystin for different clones of P. falciparum are comparable to those obtained for mammalian cell lines (0.65 μM), suggesting the presence of a conserved proteasome complex. Moreover, lactacystin was equally toxic to drug-sensitive and resistant parasites.</div>
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