Transcription Factor |
Target ORF/Genes |
References |
Evidence Code |
Evidence Experiment |
Association Type |
Strain |
Environmental Group |
Environmental Condition |
Log2FC |
|
Gat1p
|
YFL021W
|
PubMed
Coffman JA et al., Journal of bacteriology, 1997 Jun;179(11):3416-29Coffman JA et al., Journal of bacteriology, 1997 Jun;179(11):3416-29 |
Indirect |
lacZ - wt vs TF mutant |
Negative |
TCY1 |
Nitrogen source quality/availability |
Minimal medium + proline |
N/A |
PubMed
Georis I et al., Molecular and cellular biology, 2009 Jul;29(13):3803-15Georis I et al., Molecular and cellular biology, 2009 Jul;29(13):3803-15 |
Direct |
ChIP |
N/A |
S288c |
Nitrogen source quality/availability |
glutamine/proline |
N/A |
PubMed
Reimand J et al., Nucleic acids research, 2010 Aug;38(14):4768-77Reimand J et al., Nucleic acids research, 2010 Aug;38(14):4768-77 |
Indirect |
Microarray analysis - WT vs TF Deletion |
Positive |
BY4741; S288C; R1158 |
Unstressed log-phase growth (control) |
Standard YPD conditions Dataset ewxtracted from The Longhorn Array Database (LAD). Transcription factor gene deletion. |
1.7877282094361 |
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 GAT1 ORF of MT2 or YS58 strains cloned into SalI and XbaI 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 GAT1 (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 GAT1 (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
Hong J et al., eLife, 2018 Apr 5;7():Hong J et al., eLife, 2018 Apr 5;7(): |
Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Cell cycle/morphology |
Early first acidic phase (day 4): Giant colonies grown on GM solid agar (1% yeast extract, 3% glycerol, 2% agar, 30 mM CaCl2) at room temperature; colonies harvested at day 4, corresponding to the early first acidic phase. |
-3.223350679 |
| Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Cell cycle/morphology |
Middle first acidic phase (day 7): Giant colonies grown on GM solid agar (1% yeast extract, 3% glycerol, 2% agar, 30 mM CaCl2) at room temperature; colonies harvested at day 7, corresponding to the middle first acidic phase. |
-2.903040706 |
| Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Unstressed log-phase growth (control) |
Grown in synthetic complete (SC) medium at 30°C to a density of 10^7 cells per mL. Transcription factor gene deletion. |
-3.671217656 |
| Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Nitrogen source quality/availability |
Cells cultured in ammonium-limited chemostats.Strain bearing single GAT1 missense mutations gat1-1 (W321). Transcription factor gene mutation. |
-3.223350679 |
| Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Nitrogen source quality/availability |
Cells cultured in ammonium-limited chemostats.Strain bearing single GAT1 missense mutations gat1-2 (C331Y). Transcription factor gene mutation. |
-2.903040706 |
| Indirect |
RNA-seq analysis - WT vs TF Mutant |
N/A |
FY4 |
Nitrogen source quality/availability |
Cells cultured in ammonium-limited chemostats.Strain bearing single GAT1 missense mutations gat1-3 (R345G). Transcription factor gene mutation. |
-3.671217656 |