Yeastract
YEASTRACT+ INESC-ID IST IBB
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Regulation Reference(s)

The Yeastract team, is actively curating each regulation evidence code, association type and environmental condition.
Transcription
Factor
Target
ORF/Genes
References Evidence
Code
Evidence
Experiment
Association
Type
Strain Environmental
Group
Environmental
Condition
Log2FC
Rox1p YPR065W PubMed external link Deckert J et al., Molecular and cellular biology, 1995 Nov;15(11):6109-17Deckert J et al., Molecular and cellular biology, 1995 Nov;15(11):6109-17 N/A N/A S288c N/A N/A N/A
PubMed external link Deckert J et al., Genetics, 1995 Mar;139(3):1149-58Deckert J et al., Genetics, 1995 Mar;139(3):1149-58 Indirect lacZ - wt vs TF mutant Negative S288c Oxygen availability Anaerobiosis N/A
PubMed external link Harbison CT et al., Nature, 2004 Sep 2;431(7004):99-104Harbison CT et al., Nature, 2004 Sep 2;431(7004):99-104 Direct Chip-on-chip N/A S288c N/A N/A N/A
PubMed external link Chua G et al., Proceedings of the National Academy of Sciences of the United States of America, 2006 Aug 8;103(32):12045-50Chua G et al., Proceedings of the National Academy of Sciences of the United States of America, 2006 Aug 8;103(32):12045-50 Indirect Microarray analysis - wt vs TF overexpression Positive N/A Carbon source quality/availability Cells grown in selective medium supplemented with 2% raffinose before induction with 2% galactose for 3 h N/A
PubMed external link 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 mutant Positive BY4741 Stress YPD 30.C 0.1 mM H2O2 N/A
PubMed external link Castro-Prego R et al., The Biochemical journal, 2009 Dec 14;425(1):235-43Castro-Prego R et al., The Biochemical journal, 2009 Dec 14;425(1):235-43 Direct ChIP N/A S288c Oxygen availability Hypoxia N/A
PubMed external link 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. 0.38227227009137
PubMed external link Huebert DJ et al., Molecular and cellular biology, 2012 May;32(9):1645-53Huebert DJ et al., Molecular and cellular biology, 2012 May;32(9):1645-53 Indirect RT-PCR - wt vs TF mutant Negative S288c Unstressed log-phase growth (control) Normoxia N/A
PubMed external link Rossi MJ et al., Nature, 2021 Apr;592(7853):309-314Rossi MJ et al., Nature, 2021 Apr;592(7853):309-314 Direct ChIP-exo N/A BY4741 Unstressed log-phase growth (control) YPD medium, 25.C N/A
PubMed external link 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 Positive 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). 9.139802
Indirect RNA-seq analysis - WT vs TF Deletion Positive MEP Unstressed log-phase growth (control) YPD,log: Cells were grown in YP + 2% glucose (YPD) at 30°C, 200 rpm and harvested at log phase as a young control. 12.707968
PubMed external link 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 Positive 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) 13.344946
Indirect RNA-seq analysis - WT vs TF Deletion Positive 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) 15.166204