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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: J Struct Biol. 2015 Mar 9;190(2):93–114. doi: 10.1016/j.jsb.2015.02.008

Table 4.

DiCre-recombinase inducible knockouts in T. gondii effects on egress and invasion phenotypes.

Induced
Knockout
Egress Invasion Gliding Compensatory Mechanism Reference
MyoA 2% 16% 37% MyoC glideosome Egarter et al., 2014
MyoB/C 100% 100% 100% MyoA glideosome Egarter et al., 2014
MyoA/B/C 2% 5% N.D. MyoD? MyoE? (untested) Egarter et al., 2014
MLC1 5% 28% 42% MyoD-MLC2? (untested) Egarter et al., 2014
GAP45 4% 6% 100% GAP80 over-expression Frenal et al., 2014b Egarter et al., 2014
GAP80* 85% 80% N.D. GAP45 Frenal et al., 2014b
GAP40 N.D. N.D. N.D. essential Egarter et al., 2014
GAP50 N.D. N.D. N.D. essential Egarter et al., 2014
Actin 1 2% 10% 10% ? Egarter et al., 2014
Aldolase** N.D. 100% 100% GAPDH? Shen and Sibley, 2014
AMA1 N.D. ~25% 100% Other adhesins Shen and Sibley, 2014
*

Phenotype from GAP80 clonal KO line with GAP45 iKO in absence of ATc. All other clones are inducible knockouts via the DiCre-recombinase system established in T. gondii.

**

Performed in low glucose conditions to alleviate toxicity of glycolysis intermediates.