Identification and bioinformatic characterization of a multidrug resistance associated protein (ABCC) gene in Plasmodium berghei

BackgroundThe ATP-binding cassette (ABC) superfamily is one of the largest evolutionarily conserved families of proteins. ABC proteins play key roles in cellular detoxification of endobiotics and xenobiotics. Overexpression of certain ABC proteins, among them the multidrug resistance associated protein (MRP), contributes to drug resistance in organisms ranging from human neoplastic cells to parasitic protozoa. In the present study, the Plasmodium berghei mrp gene (pbmrp) was partially characterized and the predicted protein was classified using bioinformatics in order to explore its putative involvement in drug resistance.MethodsThe pbmrp gene from the P. berghei drug sensitive, N clone, was sequenced using a PCR strategy. Classification and domain organization of pbMRP were determined with bioinformatics. The Plasmodium spp. MRPs were aligned and analysed to study their conserved motifs and organization. Gene copy number and organization were determined via Southern blot analysis in both N clone and the chloroquine selected line, RC. Chromosomal Southern blots and RNase protection assays were employed to determine the chromosomal location and expression levels of pbmrp in blood stages.ResultsThe pbmrp gene is a single copy, intronless gene with a predicted open reading frame spanning 5820 nucleotides. Bioinformatic analyses show that this protein has distinctive features characteristic of the ABCC sub-family. Multiple sequence alignments reveal a high degree of conservation in the nucleotide binding and transmembrane domains within the MRPs from the Plasmodium spp. analysed. Expression of pbmrp was detected in asexual blood stages. Gene organization, copy number and mRNA expression was similar in both lines studied. A chromosomal translocation was observed in the chloroquine selected RC line, from chromosome 13/14 to chromosome 8, when compared to the drug sensitive N clone.ConclusionIn this study, the pbmrp gene was sequenced and classified as a member of the ABCC sub-family. Multiple sequence alignments reveal that this gene is homologous to the Plasmodium y. yoelii and Plasmodium knowlesi mrp, and the Plasmodium vivax and Plasmodium falciparum mrp2 genes. There were no differences in gene organization, copy number, or mRNA expression between N clone and the RC line, but a chromosomal translocation of pbmrp from chromosome 13/14 to chromosome 8 was detected in RC.

[1]  M. Ouellette,et al.  Co‐amplification of the γ‐glutamylcysteine synthetase gene gsh1 and of the ABC transporter gene pgpA in arsenite‐resistant Leishmania tarentolae , 1997, The EMBO journal.

[2]  A. Cowman,et al.  Plasmodium falciparum: chloroquine selection of a cloned line and DNA rearrangements. , 1996, Experimental parasitology.

[3]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[4]  Karl Kuchler,et al.  ABC proteins : from bacteria to man , 2003 .

[5]  S. Cole,et al.  Substrate recognition and transport by multidrug resistance protein 1 (ABCC1) , 2006, FEBS letters.

[6]  K. Kirk,et al.  Pgh1 modulates sensitivity and resistance to multiple antimalarials in Plasmodium falciparum , 2000, Nature.

[7]  Benjamin A. Shoemaker,et al.  CDD: a database of conserved domain alignments with links to domain three-dimensional structure , 2002, Nucleic Acids Res..

[8]  K. Linton,et al.  The ATP switch model for ABC transporters , 2004, Nature Structural &Molecular Biology.

[9]  S. Cole,et al.  Characterization of vincristine transport by the M(r) 190,000 multidrug resistance protein (MRP): evidence for cotransport with reduced glutathione. , 1998, Cancer research.

[10]  Li Li,et al.  PlasmoDB: the Plasmodium genome resource. An integrated database providing tools for accessing, analyzing and mapping expression and sequence data (both finished and unfinished) , 2002, Nucleic Acids Res..

[11]  J. Molez,et al.  Enzyme typing of Plasmodium falciparum from African and some other Old World countries. , 1981, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[12]  T. Tiffert,et al.  Plasmodium falciparum expresses a multidrug resistance-associated protein. , 2004, Biochemical and biophysical research communications.

[13]  D. Fidock,et al.  Decreasing pfmdr1 copy number in plasmodium falciparum malaria heightens susceptibility to mefloquine, lumefantrine, halofantrine, quinine, and artemisinin. , 2006, The Journal of infectious diseases.

[14]  D. Keppler,et al.  The apical conjugate efflux pump ABCC2 (MRP2) , 2007, Pflügers Archiv - European Journal of Physiology.

[15]  K. Nicholas,et al.  GeneDoc: Analysis and visualization of genetic variation , 1997 .

[16]  I. Pastan,et al.  MRP9, an unusual truncated member of the ABC transporter superfamily, is highly expressed in breast cancer , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Broeks,et al.  Homologues of the human multidrug resistance genes MRP and MDR contribute to heavy metal resistance in the soil nematode Caenorhabditis elegans. , 1996, The EMBO journal.

[18]  Bindu Gajria,et al.  PlasmoDB: The Plasmodium Genome Resource , 2005 .

[19]  A Elofsson,et al.  Prediction of transmembrane alpha-helices in prokaryotic membrane proteins: the dense alignment surface method. , 1997, Protein engineering.

[20]  M. Ouellette,et al.  Contribution of the Leishmania P-glycoprotein-related gene ltpgpA to oxyanion resistance. , 1994, The Journal of biological chemistry.

[21]  A. Serrano,et al.  Plasmodium berghei: analysis of the γ-glutamylcysteine synthetase gene in drug-resistant lines ☆ , 2002 .

[22]  Wei Qian,et al.  Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. , 2000, Molecular biology and evolution.

[23]  W. Peters The chemotherapy of rodent malaria, XXII. The value of drug-resistant strains of P. berghei in screening for blood schizontocidal activity. , 1975, Annals of tropical medicine and parasitology.

[24]  S. Cole,et al.  Transmembrane transport of endo- and xenobiotics by mammalian ATP-binding cassette multidrug resistance proteins. , 2006, Physiological reviews.

[25]  Neil Hall,et al.  A Plasmodium Whole-Genome Synteny Map: Indels and Synteny Breakpoints as Foci for Species-Specific Genes , 2005, PLoS pathogens.

[26]  N. Saitou,et al.  The neighbor-joining method: a new method for reconstructing phylogenetic trees. , 1987, Molecular biology and evolution.

[27]  C. Clayton,et al.  Overexpression of the putative thiol conjugate transporter TbMRPA causes melarsoprol resistance in Trypanosoma brucei , 2002, Molecular microbiology.

[28]  Patricia De la Vega,et al.  Discovery of Gene Function by Expression Profiling of the Malaria Parasite Life Cycle , 2003, Science.

[29]  J. Felsenstein Evolutionary trees from DNA sequences: A maximum likelihood approach , 2005, Journal of Molecular Evolution.

[30]  J. Carlton,et al.  Genetics of Mefloquine Resistance in the Rodent Malaria Parasite Plasmodium chabaudi , 2003, Antimicrobial Agents and Chemotherapy.

[31]  T. Horii,et al.  Big bang in the evolution of extant malaria parasites. , 2008, Molecular biology and evolution.

[32]  Plasmodium berghei: analysis of the gamma-glutamylcysteine synthetase gene in drug-resistant lines. , 2002, Experimental parasitology.

[33]  Momiao Xiong,et al.  Multiple transporters associated with malaria parasite responses to chloroquine and quinine , 2003, Molecular microbiology.

[34]  D. Bell,et al.  Isolation of MOAT-B, a widely expressed multidrug resistance-associated protein/canalicular multispecific organic anion transporter-related transporter. , 1998, Cancer research.

[35]  P. A. Rea,et al.  The Yeast Cadmium Factor Protein (YCF1) Is a Vacuolar Glutathione S-Conjugate Pump (*) , 1996, The Journal of Biological Chemistry.

[36]  C. Wilson,et al.  Amplification of a gene related to mammalian mdr genes in drug-resistant Plasmodium falciparum. , 1989, Science.

[37]  A. Krogh,et al.  Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. , 2001, Journal of molecular biology.

[38]  E. Martinoia,et al.  An ABC-transporter of Arabidopsis thaliana has both glutathione-conjugate and chlorophyll catabolite transport activity. , 1998, The Plant journal : for cell and molecular biology.

[39]  D. Fidock,et al.  Transporters involved in resistance to antimalarial drugs. , 2006, Trends in pharmacological sciences.

[40]  K. Diederichs,et al.  Crystal structure of MalK, the ATPase subunit of the trehalose/maltose ABC transporter of the archaeon Thermococcus litoralis , 2000, The EMBO journal.

[41]  C. Janse,et al.  Generation of chromosome size polymorphism during in vivo mitotic multiplication of Plasmodium berghei involves both loss and addition of subtelomeric repeat sequences. , 1990, Molecular and biochemical parasitology.

[42]  W. Peters,et al.  Chemotherapy and drug resistance in malaria. , 1970 .

[43]  K. Kohno,et al.  A human canalicular multispecific organic anion transporter (cMOAT) gene is overexpressed in cisplatin-resistant human cancer cell lines with decreased drug accumulation. , 1996, Cancer research.

[44]  G. Kruh,et al.  The MRP family of drug efflux pumps , 2003, Oncogene.

[45]  J. Wootton,et al.  Mutations in the P. falciparum digestive vacuole transmembrane protein PfCRT and evidence for their role in chloroquine resistance. , 2000, Molecular cell.

[46]  W. Peters Drug resistance in Plasmodium berghei Vincke and Lips, 1948. I. Chloroquine resistance. , 1965, Experimental parasitology.

[47]  F. Nosten,et al.  Are Transporter Genes Other than the Chloroquine Resistance Locus (pfcrt) and Multidrug Resistance Gene (pfmdr) Associated with Antimalarial Drug Resistance? , 2005, Antimicrobial Agents and Chemotherapy.

[48]  I. Pastan,et al.  MRP8, A New Member of ABC Transporter Superfamily, Identified by EST Database Mining and Gene Prediction Program, Is Highly Expressed in Breast Cancer , 2001, Molecular medicine.

[49]  M. Ouellette,et al.  Efflux systems and increased trypanothione levels in arsenite-resistant Leishmania. , 1997, Experimental parasitology.

[50]  A. Cowman,et al.  Chromosomal rearrangements and point mutations in the DHFR-TS gene of Plasmodium chabaudi under antifolate selection. , 1990, Molecular and biochemical parasitology.

[51]  P. A. Rea,et al.  AtMRP1 gene of Arabidopsis encodes a glutathione S-conjugate pump: isolation and functional definition of a plant ATP-binding cassette transporter gene. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[52]  G. Tusnády,et al.  Membrane Topology and Glycosylation of the Human Multidrug Resistance-associated Protein (*) , 1996, The Journal of Biological Chemistry.

[53]  J. Testa,et al.  Characterization of MOAT-C and MOAT-D, new members of the MRP/cMOAT subfamily of transporter proteins. , 1998, Journal of the National Cancer Institute.

[54]  Ashutosh,et al.  Molecular mechanisms of antimony resistance in Leishmania. , 2007, Journal of medical microbiology.

[55]  S. Zakeri,et al.  Quinoline resistance associated polymorphisms in the pfcrt, pfmdr1 and pfmrp genes of Plasmodium falciparum in Iran. , 2006, Acta tropica.

[56]  R. Barker,et al.  Specific DNA probe for the diagnosis of Plasmodium falciparum malaria. , 1986, Science.

[57]  K. Linton Structure and function of ABC transporters. , 2007, Physiology.

[58]  T. Uchiumi,et al.  A canalicular multispecific organic anion transporter (cMOAT) antisense cDNA enhances drug sensitivity in human hepatic cancer cells. , 1997, Cancer research.

[59]  K. Trujillo,et al.  Plasmodium berghei: identification of an mdr-like gene associated with drug resistance. , 1999, Experimental parasitology.

[60]  Rolf Apweiler,et al.  InterProScan: protein domains identifier , 2005, Nucleic Acids Res..

[61]  R. Allikmets,et al.  Complete Characterization of the Human ABC Gene Family , 2001, Journal of bioenergetics and biomembranes.

[62]  A. Cowman,et al.  Selection for mefloquine resistance in Plasmodium falciparum is linked to amplification of the pfmdr1 gene and cross-resistance to halofantrine and quinine. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[63]  David W. Deerfield,et al.  Software Development GeneDoc Analysis and Visualization of Genetic Variation , 1997 .

[64]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[65]  D. Keppler,et al.  Transport of leukotriene C4 and structurally related conjugates. , 2002, Vitamins and hormones.

[66]  P. A. Rea,et al.  AtMRP2, an Arabidopsis ATP Binding Cassette Transporter Able to Transport Glutathione S-Conjugates and Chlorophyll Catabolites: Functional Comparisons with AtMRP1 , 1998, Plant Cell.

[67]  Christopher M Waters,et al.  Dexamethasone increases expression and activity of multidrug resistance transporters at the rat blood-brain barrier. , 2008, American journal of physiology. Cell physiology.

[68]  D. Keppler,et al.  Conjugate export pumps of the multidrug resistance protein (MRP) family: localization, substrate specificity, and MRP2-mediated drug resistance. , 1999, Biochimica et biophysica acta.

[69]  S. Beverley,et al.  Functional genetic identification of PRP1, an ABC transporter superfamily member conferring pentamidine resistance in Leishmania major. , 2003, Molecular and biochemical parasitology.

[70]  E. Pizzi,et al.  The putative gene for the first enzyme of glutathione biosynthesis in Plasmodium berghei and Plasmodium falciparum. , 1999, Molecular and biochemical parasitology.

[71]  M. Ouellette,et al.  Role of the ABC Transporter PRP1 (ABCC7) in Pentamidine Resistance in Leishmania Amastigotes , 2007, Antimicrobial Agents and Chemotherapy.

[72]  K. Linton,et al.  The Escherichia coli ATP‐binding cassette (ABC) proteins , 1998, Molecular microbiology.

[73]  Michael J. Hartshorn,et al.  Structural model of ATP-binding proteing associated with cystic fibrosis, multidrug resistance and bacterial transport , 1990, Nature.

[74]  D. Keppler,et al.  Drug resistance and ATP-dependent conjugate transport mediated by the apical multidrug resistance protein, MRP2, permanently expressed in human and canine cells. , 1999, Molecular pharmacology.

[75]  D. Keppler,et al.  CHAPTER 20 – MRP2, THE APICAL EXPORT PUMP FOR ANIONIC CONJUGATES , 2003 .

[76]  A. Serrano,et al.  Identification and expression analysis of ABC genes in Plasmodium yoelii and P. berghei , 2004, Parasitology Research.

[77]  P. Leprohon,et al.  Role of the ABC Transporter MRPA (PGPA) in Antimony Resistance in Leishmania infantum Axenic and Intracellular Amastigotes , 2005, Antimicrobial Agents and Chemotherapy.

[78]  J. Testa,et al.  Analysis of the structure and expression pattern of MRP7 (ABCC10), a new member of the MRP subfamily. , 2001, Cancer letters.

[79]  A. Serrano,et al.  Plasmodium berghei and Plasmodium yoelii: molecular karyotypes of drug-resistant lines. , 1999, Experimental parasitology.