Transcription Factor |
Target ORF/Genes |
References |
Evidence Code |
Evidence Experiment |
Association Type |
Strain |
Environmental Group |
Environmental Condition |
Log2FC |
|
Rox1p
|
YAL028W
|
PubMed
Ter Linde JJ et al., Yeast (Chichester, England), 2002 Jul;19(10):825-40Ter Linde JJ et al., Yeast (Chichester, England), 2002 Jul;19(10):825-40 |
Indirect |
Microarray analysis - wt vs TF mutant |
Negative |
CEN.PK113-7D |
Carbon source quality/availability |
Steady-state chemostat cultures aerobically grown on mineral mediium containing 7.5 g/L glucose (growth-limiting nutrient) |
N/A |
PubMed
Kelley R et al., PLoS genetics, 2009 May;5(5):e1000488Kelley R et al., PLoS genetics, 2009 May;5(5):e1000488 |
Indirect |
Microarray analysis - WT vs TF Deletion |
Negative |
BY4741 |
Unstressed log-phase growth (control) |
Single colony overnight growth in 10 mL of YPD at 30°C resuspended in 100 mL of YPD media at an OD600 of 0.1 and placed in an orbital shaker at 30°C. Transcription factor gene deletion. |
-1.693508 |
| Indirect |
Microarray analysis - WT vs TF Deletion |
Negative |
BY4741 |
Stress |
Single colony overnight growth in 10 mL of YPD at 30°C resuspended in 100 mL of YPD media at an OD600 of 0.1 and placed in an orbital shaker at 30°C. Yeast cells grown to OD600 0.6 and treated with 0.1 mM H2O2 for 45 minutes. Transcription factor gene deletion. |
-1.897023 |
PubMed
Horkai D et al., PLoS biology, 2023 Aug;21(8):e3002245Horkai D et al., PLoS biology, 2023 Aug;21(8):e3002245 |
Indirect |
RNA-seq analysis - WT vs TF Deletion |
Negative |
MEP |
Carbon source quality/availability |
YPD,48h: Cells were grown in YP + 2% glucose (YPD) at 30°C, 200 rpm and mother cells were harvested 48h after estradiol addition (added at 2h post-inoculation). |
-0.744219 |
PubMed
van der Horst SC et al., Nature communications, 2025 Feb 6;16(1):1416van der Horst SC et al., Nature communications, 2025 Feb 6;16(1):1416 |
Indirect |
RNA-seq analysis - WT vs TF Deletion |
Negative |
W303 |
Cell cycle/morphology |
0 min: RNA-seq performed in YPAD medium. Overnight cultures were diluted in fresh YPAD and grown for 3 h. Cells were then synchronized in G1 by α-factor treatment for 2 h, washed once in YPAD, and released into YPAD containing 200 mM hydroxyurea (HU). Samples were collected at t=0min: immediately after α-factor synchronization (pre-HU release) |
-1.101945 |
| Indirect |
RNA-seq analysis - WT vs TF Deletion |
Negative |
W303 |
Cell cycle/morphology |
60 min: RNA-seq performed in YPAD medium. Overnight cultures were diluted in fresh YPAD and grown for 3 h. Cells were then synchronized in G1 by α-factor treatment for 2 h, washed once in YPAD, and released into YPAD containing 200 mM hydroxyurea (HU). Samples were collected at t=60min: 60 min after release into HU (replication stress condition) |
-1.330394 |