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. 2001 Feb;183(3):830–834. doi: 10.1128/JB.183.3.830-834.2001

TABLE 1.

S. cerevisiae strains used in this study

Straina Genotypeb Source or reference
463-1C MATaleu2 his3 trp1 ura3 K. Tatchelc
463-1D MATα leu2 his3 trp1 ura3 K. Tatchel
463-1C/463-1D MATa/MATα leu2/leu2 his3/his3 trp1/trp1 ura3/ura3 K. Tatchel
CJ2-A MATaupc2-1 leu2 his3 trp1 ura3 4
CJ625 MATaupc2::URA3 leu2 his3 trp1 ura3 4
H1B MATα ylr228c::LEU2 leu2 his3 trp1 ura3 This study
H1B (+) MATα ylr228c::LEU2 leu2 his3 trp1 ura3 This study
KS93 MATaupc2-1 ylr228c::LEU2 leu2 his3 trp1 ura3 This study
KS93 (+) MATaupc2-1 ylr228c::LEU2 leu2 his3 trp1 ura3 This study
KS94 (+) MATaupc2::URA3 ylr228c::LEU2 leu2 his3 trp1 ura3 This study
H1B (++) MATα ylr228c::LEU2 leu2 his3 trp1 ura3 This study
KS122 (++) MATaupc2-1 ylr228c::LEU2 leu2 his3 trp1 ura3 This study
KS119 (++) MATaupc2::URA3 ylr228c::LEU2 leu2 his3 trp1 ura3 This study
a

+, Strain is transformed with the plasmid YEp351 containing the YLR228c point mutation; ++, strain is transformed with the plasmid pRS313 containing the YLR228c point mutation. 

b

upc2  = YDR213w. 

c

Kelly Tatchel, Louisiana State University Medical Center, Shreveport, La.