MLX (gene)
From Wikipedia, the free encyclopedia
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MAX-like protein X
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| Identifiers | ||||||||||||||
| Symbol(s) | MLX; MAD7; MXD7; TCFL4 | |||||||||||||
| External IDs | OMIM: 602976 MGI: 108398 HomoloGene: 7969 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 6945 | 21428 | ||||||||||||
| Ensembl | ENSG00000108788 | ENSMUSG00000017801 | ||||||||||||
| Uniprot | Q9UH92 | Q3UQB4 | ||||||||||||
| Refseq | NM_170607 (mRNA) NP_733752 (protein) |
NM_011550 (mRNA) NP_035680 (protein) |
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| Location | Chr 17: 37.97 - 37.98 Mb | Chr 11: 100.9 - 100.91 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
MAX-like protein X, also known as MLX, is a human gene.[1]
The product of this gene belongs to the family of basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factors. These factors form heterodimers with Mad proteins and play a role in proliferation, determination and differentiation. This gene product may act to diversify Mad family function by its restricted association with a subset of the Mad family of transcriptional repressors, namely, Mad1 and Mad4. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.[1]
[edit] References
[edit] Further reading
- Rommens JM, Durocher F, McArthur J, et al. (1996). "Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21.". Genomics 28 (3): 530–42. PMID 7490091.
- Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. PMID 8889548.
- Hillier LD, Lennon G, Becker M, et al. (1997). "Generation and analysis of 280,000 human expressed sequence tags.". Genome Res. 6 (9): 807–28. PMID 8889549.
- Bjerknes M, Cheng H (1997). "TCFL4: a gene at 17q21.1 encoding a putative basic helix-loop-helix leucine-zipper transcription factor.". Gene 181 (1-2): 7–11. PMID 8973301.
- Billin AN, Eilers AL, Queva C, Ayer DE (2000). "Mlx, a novel Max-like BHLHZip protein that interacts with the Max network of transcription factors.". J. Biol. Chem. 274 (51): 36344–50. PMID 10593926.
- Meroni G, Cairo S, Merla G, et al. (2000). "Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?". Oncogene 19 (29): 3266–77. doi:. PMID 10918583.
- Billin AN, Eilers AL, Coulter KL, et al. (2000). "MondoA, a novel basic helix-loop-helix-leucine zipper transcriptional activator that constitutes a positive branch of a max-like network.". Mol. Cell. Biol. 20 (23): 8845–54. PMID 11073985.
- Cairo S, Merla G, Urbinati F, et al. (2001). "WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.". Hum. Mol. Genet. 10 (6): 617–27. PMID 11230181.
- Eilers AL, Sundwall E, Lin M, et al. (2003). "A novel heterodimerization domain, CRM1, and 14-3-3 control subcellular localization of the MondoA-Mlx heterocomplex.". Mol. Cell. Biol. 22 (24): 8514–26. PMID 12446771.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:. PMID 14702039.
- Merla G, Howald C, Antonarakis SE, Reymond A (2005). "The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3.". Hum. Mol. Genet. 13 (14): 1505–14. doi:. PMID 15163635.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:. PMID 15489334.
- Ma L, Tsatsos NG, Towle HC (2005). "Direct role of ChREBP.Mlx in regulating hepatic glucose-responsive genes.". J. Biol. Chem. 280 (12): 12019–27. doi:. PMID 15664996.
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:. PMID 16189514.
- Sans CL, Satterwhite DJ, Stoltzman CA, et al. (2006). "MondoA-Mlx heterodimers are candidate sensors of cellular energy status: mitochondrial localization and direct regulation of glycolysis.". Mol. Cell. Biol. 26 (13): 4863–71. doi:. PMID 16782875.
[edit] External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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