MXD4
From Wikipedia, the free encyclopedia
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MAX dimerization protein 4
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| Identifiers | ||||||||||||||
| Symbol(s) | MXD4; MAD4; MST149; MSTP149 | |||||||||||||
| External IDs | MGI: 104991 HomoloGene: 4712 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 10608 | 17122 | ||||||||||||
| Ensembl | ENSG00000123933 | n/a | ||||||||||||
| Uniprot | Q14582 | n/a | ||||||||||||
| Refseq | NM_006454 (mRNA) NP_006445 (protein) |
NM_010753 (mRNA) NP_034883 (protein) |
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| Location | Chr 4: 2.22 - 2.23 Mb | n/a | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
MAX dimerization protein 4, also known as MXD4, is a human gene.[1]
This gene is a member of the MAD gene family . The MAD genes encode basic helix-loop-helix-leucine zipper proteins that heterodimerize with MAX protein, forming a transcriptional repression complex. The MAD proteins compete for MAX binding with MYC, which heterodimerizes with MAX forming a transcriptional activation complex. Studies in rodents suggest that the MAD genes are tumor suppressors and contribute to the regulation of cell growth in differentiating tissues.[1]
[edit] References
[edit] Further reading
- 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.
- Marcotte R, Chen JM, Huard S, Wang E (2006). "c-Myc creates an activation loop by transcriptionally repressing its own functional inhibitor, hMad4, in young fibroblasts, a loop lost in replicatively senescent fibroblasts.". J. Cell. Biochem. 96 (5): 1071-85. doi:. PMID 16167342.
- Pope SN, Lee IR (2005). "Yeast two-hybrid identification of prostatic proteins interacting with human sex hormone-binding globulin.". J. Steroid Biochem. Mol. Biol. 94 (1-3): 203-8. doi:. PMID 15862967.
- Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4.". Nature 434 (7034): 724-31. doi:. PMID 15815621.
- 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.
- Jiang DJ, Yu HX, Hexige SY, et al. (2004). "Human liver specific transcriptional factor TCP10L binds to MAD4.". J. Biochem. Mol. Biol. 37 (4): 402-7. PMID 15469726.
- 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.
- 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.
- Kime L, Wright SC (2003). "Mad4 is regulated by a transcriptional repressor complex that contains Miz-1 and c-Myc.". Biochem. J. 370 (Pt 1): 291-8. doi:. PMID 12418961.
- 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.
- 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.
- Hurlin PJ, Quéva C, Koskinen PJ, et al. (1996). "Mad3 and Mad4: novel Max-interacting transcriptional repressors that suppress c-myc dependent transformation and are expressed during neural and epidermal differentiation.". EMBO J. 14 (22): 5646-59. PMID 8521822.
[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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