SummaryRMgm-1132
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Successful modification | The parasite was generated by the genetic modification |
The mutant contains the following genetic modification(s) | Gene disruption |
Reference (PubMed-PMID number) | Not published (yet) |
MR4 number | |
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Parent parasite used to introduce the genetic modification | |
Rodent Malaria Parasite | P. berghei |
Parent strain/line | P. berghei ANKA |
Name parent line/clone | Not applicable |
Other information parent line | |
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The mutant parasite was generated by | |
Name PI/Researcher | Koussis K; Thanasis L |
Name Group/Department | Institute of Molecular Biology and Biotechnology |
Name Institute | FORTH |
City | Heraklion |
Country | Greece |
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Name of the mutant parasite | |
RMgm number | RMgm-1132 |
Principal name | pbmemp1 - |
Alternative name | |
Standardized name | |
Is the mutant parasite cloned after genetic modification | Yes |
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Phenotype | |
Asexual blood stage | Not tested |
Gametocyte/Gamete | Not tested |
Fertilization and ookinete | Not tested |
Oocyst | Increase in oocyst numbers |
Sporozoite | Not tested |
Liver stage | Not tested |
Additional remarks phenotype | Mutant/mutation This mutant has been reported on the 2014 (25th) Annual Molecular Parasitology Meeting, Woodshole (see link for the Abstract describing this mutant). In the abstract only limited data is provided on the generation of the mutant, genotype and phenotype analyses. When this mutant is published, additional information will be added to this mutant-entry. The generation of this mutant indicates that the protein is not essential for blood stage development/multiplication. Phenotype analyses indicate that this protein has a role during mosquitoe development. !! From the Abstract: |
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Details of the target gene | |||||||||||||||||||||||||
Gene Model of Rodent Parasite | PBANKA_1362500 | ||||||||||||||||||||||||
Gene Model P. falciparum ortholog | PF3D7_1305600 | ||||||||||||||||||||||||
Gene product | site-2 protease S2P, putative | ||||||||||||||||||||||||
Gene product: Alternative name | MEMP1 | ||||||||||||||||||||||||
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Details of the genetic modification | |||||||||||||||||||||||||
Inducable system used | No | ||||||||||||||||||||||||
Additional remarks inducable system | |||||||||||||||||||||||||
Type of plasmid/construct used | not known | ||||||||||||||||||||||||
PlasmoGEM (Sanger) construct/vector used | No | ||||||||||||||||||||||||
Modified PlasmoGEM construct/vector used | No | ||||||||||||||||||||||||
Plasmid/construct map | |||||||||||||||||||||||||
Plasmid/construct sequence | |||||||||||||||||||||||||
Restriction sites to linearize plasmid | |||||||||||||||||||||||||
Partial or complete disruption of the gene | Unknown | ||||||||||||||||||||||||
Additional remarks partial/complete disruption | This mutant has been reported on the 2014 (25th) Annual Molecular Parasitology Meeting, Woodshole. In the abstract only limited data is provided on the generation of the mutant, genotype and phenotype analysis. When this mutant is published, additional information will be added to this mutant-entry. | ||||||||||||||||||||||||
Selectable marker used to select the mutant parasite | not known | ||||||||||||||||||||||||
Promoter of the selectable marker | not known | ||||||||||||||||||||||||
Selection (positive) procedure | not known | ||||||||||||||||||||||||
Selection (negative) procedure | not known | ||||||||||||||||||||||||
Additional remarks genetic modification | This mutant has been reported on the 2014 (25th) Annual Molecular Parasitology Meeting, Woodshole. In the abstract only limited data is provided on the generation of the mutant, genotype and phenotype analysis. When this mutant is published, additional information will be added to this mutant-entry. | ||||||||||||||||||||||||
Additional remarks selection procedure | |||||||||||||||||||||||||
Primer information: Primers used for amplification of the target sequences
Primer information: Primers used for amplification of the target sequences
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