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. 2008 Jul 3;47(30):7937–7946. doi: 10.1021/bi800723n

Table 1. Strains Used in This Work.

strain genotype ref
SS328 MATα ade2-101 his3Δ200 ura3-52 lys2-801 50
YG248 MATa ade2-101 ura3-52 his3Δ200 lys2-801 Δalg3::HIS3 51
YG1056 MATα ade2-101 ura3-52 his3Δ200 Δalg12::kanMX4 Δalg5::HIS3; SS328/SS330 strain background Aebi strain collection
YG1057 MATa ade2-201 ura3-52 his3Δ200 lys2-801 Δalg3::HIS3 Δalg5::HIS3; SS328/SS330 strain background Aebi strain collection
YG1128 MATa/α ade2-201/ade2-201 ura3-52/ura3-52 his3Δ200/his3Δ200 tyr1/+ lys2/+ Δrft1::HIS3/+; SS328/SS330 strain background Aebi strain collection
YCF40a MATα ade2-201 ura3-52 his3Δ200 tyr1 Δrft1::HIS3 pJH19 this study
BJ2168 MATa leu2 trp1 ura3-52 prb1-1122 pep4-3 prc1-407 gal2 52
a

The genomic copy of RFT1 is disrupted in strain YCF40; YCF40 contains URA3 plasmid pJH19 that encodes Rft1 tagged at its C-terminus with Protein A. We refer to this chimeric protein as Rft1*. YCF40 cells do not grow on minimal medium containing 5-fluoroorotic acid and uracil, indicating that the plasmid-encoded Rft1* protein is functional and required to complement the lack of RFT1 in the genome.