RMgmDB - Rodent Malaria genetically modified Parasites

Summary

RMgm-4722
Malaria parasiteP. yoelii
Genotype
TaggedGene model (rodent): py17X_1354300; Gene model (P.falciparum): Not available; Gene product: conserved Plasmodium protein, unknown function
Name tag: GFP
Phenotype Sporozoite;
Last modified: 6 February 2020, 12:54
  *RMgm-4722
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) : 31673027
MR4 number
Parent parasite used to introduce the genetic modification
Rodent Malaria ParasiteP. yoelii
Parent strain/lineP. y. yoelii 17XNL
Name parent line/clone Not applicable
Other information parent line
The mutant parasite was generated by
Name PI/ResearcherLindner, SE, Kappe SHI
Name Group/DepartmentDepartment of Global Health
Name InstituteUniversity of Washington
CitySeattle
CountryUS
Name of the mutant parasite
RMgm numberRMgm-4722
Principal namepy17X_1354300-GFP
Alternative name
Standardized name
Is the mutant parasite cloned after genetic modificationYes
Phenotype
Asexual blood stageNot tested
Gametocyte/GameteNot tested
Fertilization and ookineteNot tested
OocystNot tested
SporozoitePY17X_1354300, is one of the most abundant mRNAs in P. yoelii salivary gland sporozoites (99.5th percentile) but was among the least abundant proteins detected in sporozoites, indicating translational repression. In agreement with the proteomic data, we did not detect the presence of PY17X_1354300::GFP protein using anti-GFP antibodies in sporozoites.
Liver stageNot tested
Additional remarks phenotype

Mutant/mutation
The mutant expresses a C-terminal GFP-tagged version of py17X_1354300

Protein (function)

PY17X_1354300, is one of the most abundant mRNAs in P. yoelii salivary gland sporozoites (99.5th percentile) but was among the least abundant proteins detected in sporozoites, indicating translational repression.

Phenotype
PY17X_1354300, is one of the most abundant mRNAs in P. yoelii salivary gland sporozoites (99.5th percentile) but was among the least abundant proteins detected in sporozoites, indicating translational repression.
In agreement with the proteomic data, we did not detect the presence of PY17X_1354300::GFP protein using anti-GFP antibodies in sporozoites.

Additional information

Other mutants


  Tagged: Mutant parasite with a tagged gene
Details of the target gene
Gene Model of Rodent Parasite py17X_1354300
Gene Model P. falciparum ortholog Not available
Gene productconserved Plasmodium protein, unknown function
Gene product: Alternative name
Details of the genetic modification
Name of the tagGFP
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 parasitehdhfr
Promoter of the selectable markereef1a
Selection (positive) procedurepyrimethamine
Selection (negative) procedureNo
Additional remarks genetic modificationReverse genetic modification of P. yoelii parasites. Plasmodium yoelii (17XNL strain) was genetically modified using conventional, double homologous recombination approaches with the pDEF plasmid vector. The 3′ end of py17X_1354300 or pyuis12 (PY17X_0507300) was modified by the addition of the GFPmut2 coding sequence prior to the stop codon. Transgenic parasites were identified by genotyping PCR, with independent transgenic clones being isolated by limiting dilution cloning. Clonal parasites were transmitted to A. stephensi mosquitoes to produce salivary gland sporozoites.
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