Transcription Factor |
Target ORF/Genes |
References |
Evidence Code |
Evidence Experiment |
Association Type |
Strain |
Environmental Group |
Environmental Condition |
Log2FC |
|
Gln3p
|
YDR421W
|
PubMed
Staschke KA et al., The Journal of biological chemistry, 2010 May 28;285(22):16893-911Staschke KA et al., The Journal of biological chemistry, 2010 May 28;285(22):16893-911 |
Indirect |
Microarray analysis - WT vs TF Deletion |
Positive |
WY798 |
Nitrogen source quality/availability |
Grown in synthetic medium (SD) (2% dextrose, 0.5% ammonium sulfate) + amino acids w/o histidine (SC medium). Cells treated for 1 h with 200 nM rapamycin. Transcription factor gene deletion. |
0.13750352 |
PubMed
Lee K et al., Molecular microbiology, 2013 Jun;88(6):1120-34Lee K et al., Molecular microbiology, 2013 Jun;88(6):1120-34 |
Indirect |
RT-PCR - wt vs TF mutant |
Positive |
S288c |
Stress |
BY4741 gln3DELTA and gln3DELTAgat1DELTA cells cultured in YPD medium until early exponential phase and then treated with 0.2 microg ml−1 rapamycin (Rap) for 1 h. |
N/A |
PubMed
Chen X et al., Journal of biotechnology, 2017 Jan 20;242():83-91Chen X et al., Journal of biotechnology, 2017 Jan 20;242():83-91 |
Indirect |
RT-PCR - wt vs TF mutant |
Positive |
S288c |
Unstressed log-phase growth (control) |
YS58 strain with plasmid containing GLN3 ORF of MT2 or YS58 strains cloned into SalI and SacI of ADH1 promoter and terminator cloned into Escherichia coli-Yeast shuttle vector - Overexpression of GLN3; cells grown in synthetic complete medium |
N/A |
| Indirect |
RT-PCR - wt vs TF mutant |
Positive |
YS58 |
Nitrogen source quality/availability |
wt and GLN3 (gene from MT2 strain) over-expressing strains were grown for 12, 24, 48 and 72 hours, in medium used for fermentation containing 30 g/L glucose, 0.5 g/L MgSO4·7H2O, 0.5 g/L KH2PO4, and 5 g/L L-phenylalanine (l-Phe), as a sole nitrogen source. |
N/A |
| Indirect |
RT-PCR - wt vs TF mutant |
Positive |
YS58 |
Nitrogen source quality/availability |
wt and GLN3 (gene from YS58 strain) over-expressing strains were grown for 12, 24, 48 and 72 hours in medium used for fermentation containing 30 g/L glucose, 0.5 g/L MgSO4·7H2O, 0.5 g/L KH2PO4, and 5 g/L L-phenylalanine (l-Phe), as a sole nitrogen source. |
N/A |
PubMed
Branco J et al., Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2022 Dec;28(12):1655.e5-1655.e8Branco J et al., Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2022 Dec;28(12):1655.e5-1655.e8 |
Indirect |
RT-PCR - wt vs TF mutant |
Positive |
BY4741 |
Nitrogen source quality/availability |
YPD medium + Rap + 6h during whole-cell bioconversion |
N/A |