RMgmDB - Rodent Malaria genetically modified Parasites

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Summary

RMgm-1173
Malaria parasiteP. yoelii
Genotype
TaggedGene model (rodent): PY17X_1339000; Gene model (P.falciparum): PF3D7_1471100; Gene product: exported protein 2 (EXP2)
Name tag: triple-HA
Phenotype Asexual bloodstage;
Last modified: 30 July 2015, 16:20
  *RMgm-1173
Successful modificationThe parasite was generated by the genetic modification
The mutant contains the following genetic modification(s) Gene tagging
Reference (PubMed-PMID number) Reference 1 (PMID number) : 25662767
MR4 number
Parent parasite used to introduce the genetic modification
Rodent Malaria ParasiteP. yoelii
Parent strain/lineP. y. yoelii 17X
Name parent line/clone Not applicable
Other information parent line
The mutant parasite was generated by
Name PI/ResearcherMeibalan, E; Burns, J.M.
Name Group/DepartmentCenter for Molecular Parasitology
Name InstituteDepartment of Microbiology and Immunology
CityDrexel University, Philadelphia PA
CountryUSA
Name of the mutant parasite
RMgm numberRMgm-1173
Principal namePyExp2-3HA
Alternative name
Standardized name
Is the mutant parasite cloned after genetic modificationYes
Phenotype
Asexual blood stageEXP2 was found to be localized to the Parasitophorous Vacuole Membrane (PVM) of blood stgaes. In addition evidence is presented for a location to (spherical) vesicles in the reticulocyte cytoplasm that appeared to be distinct from the PVM.
Gametocyte/GameteNot tested
Fertilization and ookineteNot tested
OocystNot tested
SporozoiteNot tested
Liver stageNot tested
Additional remarks phenotype

Mutant/mutation
The mutant expresses a C-terminal 3x-HA-tagged version of EXP2.

Protein (function)
Plasmodium parasites remodel their vertebrate host cells by translocating hundreds of proteins across an encasing membrane into the host cell cytosol via a putative export machinery termed PTEX (Plasmodium Translocon of EXported protein). EXP2 has have been identified as a member of the PTEX complex.
Attempts to disrupt the exp2 gene of P. berghei and P. yoeili were unsuccessful, indicating an essential role of EXP2 in blood stages

Phenotype
EXP2 was found to be localized to the Parasitophorous Vacuole Membrane (PVM) of blood stgaes. In addition evidence is presented for a location to (spherical) vesicles in the reticulocyte cytoplasm that appeared to be distinct from the PVM.

Additional information

Other mutants


  Tagged: Mutant parasite with a tagged gene
Details of the target gene
Gene Model of Rodent Parasite PY17X_1339000
Gene Model P. falciparum ortholog PF3D7_1471100
Gene productexported protein 2
Gene product: Alternative nameEXP2
Details of the genetic modification
Name of the tagtriple-HA
Details of taggingC-terminal
Additional remarks: tagging
Commercial source of tag-antibodies
Type of plasmid/construct(Linear) plasmid single cross-over
PlasmoGEM (Sanger) construct/vector usedNo
Modified PlasmoGEM construct/vector usedNo
Plasmid/construct map
Plasmid/construct sequence
Restriction sites to linearize plasmid
Selectable marker used to select the mutant parasitetgdhfr
Promoter of the selectable markerpbdhfr
Selection (positive) procedurepyrimethamine
Selection (negative) procedureNo
Additional remarks genetic modificationTo tag the pyexp2 gene, a single cross-over recombination strategy was used. The pSE02-3HA plasmid containing pyrimethamine resistant Tg-dhfr-ts as a selectable marker was used to generate the tagging construct. A 495 bp fragment from the 3’ end of the pyexp2 gene was amplified from P. yoelii 17X genomic DNA and cloned into pSE02-3HA preceding the triple HA sequence resulting in the construct pSE02-3’Exp2-3HA. Plasmid DNA was isolated as above and linearized by digestion with EcoRI prior to transfection.
Additional remarks selection procedure
Primer information: Primers used for amplification of the target sequences  Click to view information
Primer information: Primers used for amplification of the target sequences  Click to hide information
Sequence Primer 1
Additional information primer 1
Sequence Primer 2
Additional information primer 2
Sequence Primer 3
Additional information primer 3
Sequence Primer 4
Additional information primer 4
Sequence Primer 5
Additional information primer 5
Sequence Primer 6
Additional information primer 6