| Standard Name | MET31 |
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| Systematic Name | YPL038W |
| Feature Type | ORF, Verified |
| Description | Zinc-finger DNA-binding transcription factor; targets strong transcriptional activator Met4p to promoters of sulfur metabolic genes; involved in transcriptional regulation of the methionine biosynthetic genes; feedforward loop controlling expression of MET32 and the lack of such a loop for MET31 may account for the differential actions of Met31p and Met32p; MET31 has a paralog, MET32, that arose from the whole genome duplication (1, 2, 3 and see Summary Paragraph) |
| Name Description | METhionine requiring 1 |
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| View Computational GO annotations for MET31 | |
| Molecular Function | |
| Manually curated | |
| High-throughput | |
| Biological Process | |
| Manually curated | |
| Cellular Component | |
| High-throughput |
| Binding motifs | Predicted MET31 Binding Site Locations |
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| Regulatory modules | predicted: stressResponse (463) predicted: cellcycle (299) predicted: stressResponse (463) predicted: cellcycle (299) |
| Resources |
| Large-scale survey | |
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| null | |
| overexpression | |
| Resources |
| 51 total interaction(s) for 37 unique genes/features. | |
| Physical Interactions |
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| Localization | |
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| Phosphorylation | PhosphoGRID | PhosphoPep Database |
| Structure | |
| Homologs |
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| Last Update | Coordinates: 2011-02-03 | Sequence: 1996-07-31 | ||||||||||||
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| S288C only | |
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| S288C vs. other species | |
| S288C vs. other strains |
| External Links | All Associated Seq | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB |
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| Primary SGDID | S000005959 |
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MET31 encodes a DNA-binding protein involved in the transcriptional control of genes involved in sulfur metabolism (1, 4, 5). Transcription of these genes is driven by large multisubunit complexes that assemble on their 5' upstream regions. Depending on the target, different combinations of the Cbf1p, Met28p, Met31p, and Met32p factors are assembled and tether the transcription factor Met4p to the DNA (6, 4, 5). Met31p, itself devoid of any intrinsic transcription activation function, appears not to act during the transcriptional regulation of all of the MET genes, but recruits Met4p to the promoters of some of the methionine biosynthetic genes, and is required for their expression (1, 7, 4). Met31p and Met32p are highly-related (46% identical) zinc finger-containing proteins, each containing an amino-terminal zinc finger of the CC/HH type, and a carboxy-terminal zinc finger of the CC/HC type (1, 8). Both proteins recognize and bind the upstream element 5'-AAACTGTGG-3', and the binding of Cbf1p in the vicinity of this motif enhances this affinity (9). The function of Met31p during the transcriptional regulation of the sulfate assimilation pathway varies from one gene to another, as Met31p seems to function as a negative regulatory factor at the MET25 promoter region, but as an essential positive effector at the MET3 and MET14 promoter regions (1, 8). The function of Met31p is not restricted to these pathways, however, as it is also involved in regulating GSH1 expression in response to cadmium (7), and may play a role in coregulating genes involved in copper and iron metabolism (10).
| 1) | Blaiseau PL, et al. (1997) Met31p and Met32p, two related zinc finger proteins, are involved in transcriptional regulation of yeast sulfur amino acid metabolism. Mol Cell Biol 17(7):3640-8 |
| 2) | Byrne KP and Wolfe KH (2005) The Yeast Gene Order Browser: combining curated homology and syntenic context reveals gene fate in polyploid species. Genome Res 15(10):1456-61 |
| 3) | McIsaac RS, et al. (2012) Perturbation-based analysis and modeling of combinatorial regulation in the yeast sulfur assimilation pathway. Mol Biol Cell 23(15):2993-3007 |
| 4) | Patton EE, et al. (2000) SCF(Met30)-mediated control of the transcriptional activator Met4 is required for the G(1)-S transition. EMBO J 19(7):1613-24 |
| 5) | Rouillon A, et al. (2000) Feedback-regulated degradation of the transcriptional activator Met4 is triggered by the SCF(Met30 )complex. EMBO J 19(2):282-94 |
| 6) | Craig KL and Tyers M (1999) The F-box: a new motif for ubiquitin dependent proteolysis in cell cycle regulation and signal transduction. Prog Biophys Mol Biol 72(3):299-328 |
| 7) | Dormer UH, et al. (2000) Cadmium-inducible expression of the yeast GSH1 gene requires a functional sulfur-amino acid regulatory network. J Biol Chem 275(42):32611-6 |
| 8) | Thomas D and Surdin-Kerjan Y (1997) Metabolism of sulfur amino acids in Saccharomyces cerevisiae. Microbiol Mol Biol Rev 61(4):503-32 |
| 9) | Blaiseau PL and Thomas D (1998) Multiple transcriptional activation complexes tether the yeast activator Met4 to DNA. EMBO J 17(21):6327-36 |
| 10) | Moler EJ, et al. (2000) Integrating naive Bayes models and external knowledge to examine copper and iron homeostasis in S. cerevisiae. Physiol Genomics 4(2):127-135 |
| 11) | Badis G, et al. (2008) A library of yeast transcription factor motifs reveals a widespread function for Rsc3 in targeting nucleosome exclusion at promoters. Mol Cell 32(6):878-87 |






