| Standard Name | MEK1 1 |
|---|---|
| Systematic Name | YOR351C |
| Alias | MRE4 2 |
| Feature Type | ORF, Verified |
| Description | Meiosis-specific serine/threonine protein kinase, functions in meiotic checkpoint, promotes recombination between homologous chromosomes by suppressing double strand break repair between sister chromatids (1, 2, 3, 4, 5 and see Summary Paragraph) |
| Name Description | MEiotic Kinase 1 |
| Chromosomal Location | |
|---|---|
| Note: this feature is encoded on the Crick strand. | |
| Genetic position: 175 cM |
| View Computational GO annotations for MEK1 | |
| Molecular Function | |
| Manually curated | |
| High-throughput | |
| Biological Process | |
| Manually curated | |
| High-throughput | |
| Cellular Component | |
| Manually curated |
| Classical genetics | |
|---|---|
| null | |
| Large-scale survey | |
| null |
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| overexpression | |
| Resources |
| 177 total interaction(s) for 144 unique genes/features. | |
| Physical Interactions |
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| Genetic Interactions |
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| Resources |
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| Resources |
| Localization | |
|---|---|
| Phosphorylation | PhosphoGRID | PhosphoPep Database |
| Structure | |
| Homologs |
| Note: this feature is encoded on the Crick strand. | |||||||||||||
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| Genetic position: 175 cM | |||||||||||||
| Last Update | Coordinates: 2011-02-03 | Sequence: 1996-07-31 | ||||||||||||
| Subfeature details |
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| Retrieve sequences | |||||||||||||
| S288C only | |
|---|---|
| S288C vs. other species | |
| S288C vs. other strains |
| External Links | All Associated Seq | E.C. | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB |
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| Primary SGDID | S000005878 |
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Red1p, Hop1p, and Mek1p are components of the axial element protein cores in synaptonemal complexes (6). Synaptonemal complexes are found at synapses between homologous chromosomes during meiosis, and form when sister chromatids condense upon axial elements (6). Maintenance of appropriate stoichiometry between Red1p, Hop1p, and Mek1p is important for effective chromosome segregation and for the meiotic recombination checkpoint (7). Red1p, Hop1p and Mek1p are also necessary for normal levels of double-strand break (DSB) formation (8), and are required to ensure that crossovers occur between homologous chromosomes and not between sister chromatids (7). Red1p is a multifunctional protein required for
| 1) | Rockmill B and Roeder GS (1991) A meiosis-specific protein kinase homolog required for chromosome synapsis and recombination. Genes Dev 5(12B):2392-404 |
| 2) | Leem SH and Ogawa H (1992) The MRE4 gene encodes a novel protein kinase homologue required for meiotic recombination in Saccharomyces cerevisiae. Nucleic Acids Res 20(3):449-57 |
| 3) | Bailis JM, et al. (2000) Bypass of a meiotic checkpoint by overproduction of meiotic chromosomal proteins. Mol Cell Biol 20(13):4838-48 |
| 4) | Bailis JM and Roeder GS (2000) Pachytene exit controlled by reversal of Mek1-dependent phosphorylation. Cell 101(2):211-21 |
| 5) | Niu H, et al. (2007) Mek1 kinase is regulated to suppress double-strand break repair between sister chromatids during budding yeast meiosis. Mol Cell Biol 27(15):5456-67 |
| 6) | de los Santos T, et al. (2001) A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiae. Genetics 159(4):1511-25 |
| 7) | Wan L, et al. (2004) Mek1 kinase activity functions downstream of RED1 in the regulation of meiotic double strand break repair in budding yeast. Mol Biol Cell 15(1):11-23 |
| 8) | Prieler S, et al. (2005) The control of Spo11's interaction with meiotic recombination hotspots. Genes Dev 19(2):255-69 |
| 9) | Malone RE, et al. (2004) The signal from the initiation of meiotic recombination to the first division of meiosis. Eukaryot Cell 3(3):598-609 |
| 10) | Woltering D, et al. (2000) Meiotic segregation, synapsis, and recombination checkpoint functions require physical interaction between the chromosomal proteins Red1p and Hop1p. Mol Cell Biol 20(18):6646-58 |
| 11) | Zierhut C, et al. (2004) Mnd1 is required for meiotic interhomolog repair. Curr Biol 14(9):752-62 |





