TABLE 3.
Class of mutation | eIF4E form | In vitro cap bindinga,b | In vitro eIF4G bindingb | Virus rescuec | Yeast rescued |
---|---|---|---|---|---|
mo10 allele | eIF4E0 | + | + | + | + |
mo11 allele | eIF4E1 | ± | NT | − | + |
mo12 allele | eIF4E2 | ± | NT | − | + |
eIF4G binding | E91A | + | ± | + | + |
W94A | + | ± | + | + | |
G156A | + | ± | + | + | |
E157A | + | ± | + | −* | |
Cap binding | W64A | − | NT | − | − |
W77L | ± | NT | − | − | |
W123A | − | NT | + | − | |
R173A | + | NT | − | − | |
W182A | − | NT | − | − | |
S223L | + | NT | + | + | |
Outer surface | F65A | ± | NT | − | − |
R82L | + | NT | + | + | |
Y113A | + | NT | + | + | |
A174P | ± | NT | + | −* |
Estimated by cap affinity chromatography.
+, present; −, absent; ±, binding is affected, but not fully abolished; NT, not tested.
+, the eIF4E form is able to complement LMV infection in resistant plants; −, no complementation occurs.
10× serial dilutions of yeast strain J055 transformed with plasmids p426GPD-4E were plated on glucose selective medium. +, 100× or 1,000× dilutions grew on glucose-containing medium; -, these dilutions did not grow (behavior was identical to that of the negative control, cells transformed with the plasmid p426GPD); *, in only one experiment of 4 did cells grow for a 10× dilution, but none grew for the 100× and 1,000× serial dilutions.