Summary

RMgm-90
Malaria parasiteP. berghei
Genotype
DisruptedGene model (rodent): PBANKA_0209200; Gene model (P.falciparum): PF3D7_0103900; Gene product: parasite-infected erythrocyte surface protein (PIESP15, parasite infected erythrocyte surface protein 15)
PhenotypeNo phenotype has been described
Last modified: 19 February 2009, 20:57
  *RMgm-90
Successful modificationThe parasite was generated by the genetic modification
The mutant contains the following genetic modification(s) Gene disruption
Reference (PubMed-PMID number) Reference 1 (PMID number) : 18761621
MR4 number
Parent parasite used to introduce the genetic modification
Rodent Malaria ParasiteP. berghei
Parent strain/lineP. berghei ANKA
Name parent line/clone P. berghei ANKA 2.34
Other information parent lineP. berghei ANKA 2.34 is a cloned, gametocyte producer line of the ANKA strain (PubMed: PMID: 15137943).
The mutant parasite was generated by
Name PI/ResearcherA. Ecker; R.E. Sinden
Name Group/DepartmentDivision of Cell and Molecular Biology
Name InstituteImperial College
CityLondon
CountryUnited Kingdom
Name of the mutant parasite
RMgm numberRMgm-90
Principal name∆piesp15
Alternative name
Standardized name
Is the mutant parasite cloned after genetic modificationYes
Phenotype
Asexual blood stageNot different from wild type
Gametocyte/GameteNot different from wild type
Fertilization and ookineteNot different from wild type
OocystNot different from wild type
SporozoiteNot different from wild type
Liver stageNot different from wild type
Additional remarks phenotype

Mutant/mutation
The mutant lacks expression of PIESP15 (parasite infected erythrocyte surface protein 15; Florens, L., 2004, Mol. Biochem. Parasitol. 135, 1-11).

Protein (function)
Unknown. The protein is detected in a proteome analyses of ookinetes and the surface of infected red blood cells and contains a concanavalin A-like lectin/glucanase domain (carbohydrate binding).

Phenotype
The lack of expression of PIESP15 does not result in a clear phenotype. In this study no in depht analysis of the phenotype of the different life cycle stages has been performed. Numbers of oocysts and salivary gland sporozoites in Anopheles stephensi are normal. The mutant could 'easily be transmitted' by A. stephensi.


  Disrupted: Mutant parasite with a disrupted gene
Details of the target gene
Gene Model of Rodent Parasite PBANKA_0209200
Gene Model P. falciparum ortholog PF3D7_0103900
Gene productparasite-infected erythrocyte surface protein
Gene product: Alternative namePIESP15, parasite infected erythrocyte surface protein 15
Details of the genetic modification
Inducable system usedNo
Additional remarks inducable system
Type of plasmid/construct usedPlasmid double cross-over
PlasmoGEM (Sanger) construct/vector usedNo
Modified PlasmoGEM construct/vector usedNo
Plasmid/construct map
Plasmid/construct sequence
Restriction sites to linearize plasmid
Partial or complete disruption of the genePartial
Additional remarks partial/complete disruption Gene disruption (fragment encoding C-term. 119(Py) amino acids retained
Selectable marker used to select the mutant parasitetgdhfr
Promoter of the selectable markerpbdhfr
Selection (positive) procedurepyrimethamine
Selection (negative) procedureNo
Additional remarks genetic modification
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 1GGGGTACCACTGCCGTTTTGCACATATTGAC
Additional information primer 1AE18a (KpnI); 5'
Sequence Primer 2TTGGGCCCACACTATGGAGCTTTCACAGGTG
Additional information primer 2AE18b (ApaI); 5'
Sequence Primer 3TGAATTCATATTCATAATATGCAAGATGAG
Additional information primer 3AE18c (EcoRI); 3'
Sequence Primer 4TCCCCGCGGAATATGTTTTTTTTCAACATCTC
Additional information primer 4AE18d (Sac II); 3'
Sequence Primer 5
Additional information primer 5
Sequence Primer 6
Additional information primer 6