Disruptability [+]

Species Disruptability Reference Submitter
P. berghei ANKA
Possible
RMgm-5209 Imported from RMgmDB
P. falciparum 3D7
Possible
USF piggyBac screen (Insert. mut.) USF PiggyBac Screen
P. falciparum 3D7
Possible
31559936
"PfDPY19 gene disruption was not associated with a growth phenotype, not even under endoplasmic reticulum (ER)-stressing conditions that could impair protein folding. The data presented in this work strongly suggests that PfDPY19 is unlikely to play a critical role in the asexual blood stages of the parasite, at least under in vitro conditions. "
Theo Sanderson, Francis Crick Institute
P. falciparum 3D7
Possible
35906227
\'We further show that genetic disruption of DPY19 in P. falciparum is necessary and sufficient to prevent C-mannosylation in the parasite, impair egress following gametocyte activation and abrogate ookinete infection of the mosquito midgut. Complementation of DPY19 restored the transmission defect and re-instated C-mannosylation activity, definitively validating tryptophan C-mannosylation as essential for P. falciparum infection of the mosquito, which is critical for onward transmission of the parasite.\'
Theo Sanderson, Francis Crick Institute

Mutant phenotypes [+]

Species Stage Phenotype Reference Submitter
P. berghei ANKA Asexual
No difference
RMgm-5209 Imported from RMgmDB
P. berghei ANKA Gametocyte
No difference
RMgm-5209 Imported from RMgmDB
P. berghei ANKA Ookinete
Difference from wild-type
RMgm-5209
Normal, wild-type gametocyte and ookinete production. However, ookinetes showed strongly reduced motility and motion velocity. No oocysts are formed
Imported from RMgmDB
P. berghei ANKA Oocyst
Difference from wild-type
RMgm-5209
No oocyst formation
Imported from RMgmDB
P. berghei ANKA Sporozoite
Difference from wild-type
RMgm-5209
No oocyst and sporozoite formation
Imported from RMgmDB
P. falciparum 3D7 Asexual
No difference
31559936
"PfDPY19 gene disruption was not associated with a growth phenotype, not even under endoplasmic reticulum (ER)-stressing conditions that could impair protein folding. The data presented in this work strongly suggests that PfDPY19 is unlikely to play a critical role in the asexual blood stages of the parasite, at least under in vitro conditions. "
Theo Sanderson, Francis Crick Institute
P. falciparum 3D7 Oocyst
Attenuated
35906227
\'We further show that genetic disruption of DPY19 in P. falciparum is necessary and sufficient to prevent C-mannosylation in the parasite, impair egress following gametocyte activation and abrogate ookinete infection of the mosquito midgut. Complementation of DPY19 restored the transmission defect and re-instated C-mannosylation activity, definitively validating tryptophan C-mannosylation as essential for P. falciparum infection of the mosquito, which is critical for onward transmission of the parasite.\'
Theo Sanderson, Francis Crick Institute

More information

PlasmoDB PBANKA_1224500
GeneDB PBANKA_1224500
Malaria Metabolic Pathways Localisation images
Pathways mapped to
Previous ID(s) PB001093.00.0, PBANKA_122450
Orthologs PCHAS_1225100 , PF3D7_0806200 , PKNH_0112700 , PVP01_0114300 , PVX_088240 , PY17X_1227700
Google Scholar Search for all mentions of this gene