This table describes some commonly used auxotrophic markers (along with some novel useful markers); it was obtained from Brachmann et al. (1998) "Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications." Yeast Volume 14, pp 115-132.
Please send e-mail to the curators at SGD at yeast-curator@genome.stanford.edu if you have additions or modifications you would like to suggest.
| Allele | Deleted ORF? | Reverts? | Notes | Molecular descriptiona | Reference |
|---|---|---|---|---|---|
| ade1-14 | no | yes | red colonies | TGG-to-TGA nonsense change at codon 244; GGA-to-GAA missense change at codon 185. | Nakayishiki et al. 2001 |
| ade2-1 | no | yes | ochre mutation | TTA-to-TTG silent change at codon 9, GAA-to-TAA ochre nonsense change at codon 64, AGA-to-GGA missense change at codon 101, GTT-to-GTC silent change at codon 124, ACG-to-ACA silent change at codon 539. |
Rodney Rothstein, Personal communication to SGD. |
| ade2-101 | no | yes | ochre mutation, red colonies | G to T transversion at nucleotide 190, changing amino acid 64 from a Glu to a Stop | Gai and Voytas, 2005 |
| ade2-BglII | no | no | red colonies | frameshift (BglII site filled in at position 592) | Engebrecht and Roeder 1990 |
| can1-100 | no | yes | ochre mutation | AAA-to-TAA ochre nonsense change at codon 47 | Rodney Rothstein, Personal communication to SGD. |
| his3delta200 | yes | no | Cold sensitive; high frequency of petite formation, especially
during transformation. Note that this deletion damages the PET56 promoter. See Zhang et al., (2003) for a discussion of this issue. |
1 kb deletion, (-205 to 835) | Struhl 1985; Fasullo and Davis 1988; Siram et al. YGM RNA processing mtg 1993 |
| his3delta1 | partial | no | - | 187 bp HindIII-HindIII internal (305 to 492) | Scherer and Davis 1979 |
| his3-11,15 | no | no | double mutant | G deletion at nucleotide 208, G deletion at nucleotide 319. |
Rodney Rothstein, Personal communication to SGD. |
| leu2delta1 | partial | no | - | 0.6 kb deletion, EcoRI-ClaI internal (163 to 649) | Sikorski and Hieter 1989 |
| leu2-3,112 | no | no | double mutant | GTC-to-GTT silent change at codon 56, GTT-to-GCT missene change at codon 69, G insertion at nucleotide 249, G insertion at nucleotide 792, GTT-to-GTC silent change at codon 299, GAC-to-AAC missense change at codon 300. |
Hinnen et al. 1978; Gaber and Culbertson 1982; Meira LB et al., 1995; Rodney Rothstein, Personal communication to SGD. |
| lys2-801 | no | yes | amber mutation | - | - |
| lys2delta202 | partial | no | - | 1.0 kb deletion, XhoI-HpaI internal (1813 to 2864) | Winston et al. 1995 |
| trp1delta1 | yes | no | cold sensitiveb, weak galactose inducer (deletes GAL3 UAS), removes ARS1, also called trp1-901 | 1.45 kb deletion, EcoRI-EcoRI (-102 to 1352) | Sikorski and Hieter 1989 |
| trp1delta63 | partial | no | cold sensitiveb | 0.6 kb deletion, EcoRI-HindIII (-102 to 513) | Sikorski and Hieter 1989 |
| trp1-1 | no | yes | amber mutation | GAG-to-TAG amber nonsense change at codon 83 | McDonald, et al. 1997 |
| trp1-289 | no | yes | cold sensitiveb | C to T at residue 403 of the coding sequence, changing residue 135 from glutamine to an amber stop codon. | Brian Green and Joachim Li, unpublished results |
| ura3-52 | no | no | - | Ty1 insertion (transcribing left to right) at pos. 121 | Rose and Winston 1984 |
| ura3-1 | no | yes | - | G to A transition at residue 701 of the coding sequence, changing residue 234 from glycine to glutamine | Yan Li, Glenn Manthey, and Adam Bailis, unpublished results | The following new alleles listed below are described in Brachmann et al. 1998 |
| ade2delta::hisG | no | no | - | - | (Aparicio et al. 1991) |
| leu2delta0 | yes | no | designer deletion | - | Brachmann et al. 1998 |
| lys2delta0 | yes | no | designer deletion | - | Brachmann et al. 1998 |
| met15delta0 | yes | no | designer deletion | - | Brachmann et al. 1998 |
| ura3delta0 | yes | no | designer deletion | - | Brachmann et al. 1998 |
bAll trp- strains are cold sensitive (Singh and Manney 1974).