MFNG
From Wikipedia, the free encyclopedia
MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
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Identifiers | ||||||||||||||
Symbol(s) | MFNG; | |||||||||||||
External IDs | OMIM: 602577 MGI: 1095404 HomoloGene: 1803 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 4242 | 17305 | ||||||||||||
Ensembl | ENSG00000100060 | ENSMUSG00000018169 | ||||||||||||
Uniprot | O00587 | Q3UPI0 | ||||||||||||
Refseq | NM_002405 (mRNA) NP_002396 (protein) |
XM_984857 (mRNA) XP_989951 (protein) |
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Location | Chr 22: 36.2 - 36.21 Mb | Chr 15: 78.58 - 78.6 Mb | ||||||||||||
Pubmed search | [1] | [2] |
MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, also known as MFNG, is a human gene.[1]
This gene is a member of the fringe gene family which also includes Radical and Lunatic fringe. They all encode evolutionarily conserved secreted proteins that act in the Notch receptor pathway to demarcate boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, fringe proteins have a fucose-specific beta1,3 N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling.[1]
[edit] References
[edit] Further reading
- Johnston SH, Rauskolb C, Wilson R, et al. (1997). "A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway.". Development 124 (11): 2245-54. PMID 9187150.
- Cohen B, Bashirullah A, Dagnino L, et al. (1997). "Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila.". Nat. Genet. 16 (3): 283-8. doi: . PMID 9207795.
- Egan S, Herbrick JA, Tsui LC, et al. (1999). "Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12.". Genomics 54 (3): 576-7. doi: . PMID 9878264.
- Moran JL, Johnston SH, Rauskolb C, et al. (1999). "Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes.". Mamm. Genome 10 (6): 535-41. PMID 10341080.
- Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22.". Nature 402 (6761): 489-95. doi: . PMID 10591208.
- Van Tine BA, Knops J, Shaw GM, May WA (2000). "Assignment of human MFNG, manic fringe Drosophila homolog, to 22q13.1 using tyramide fluorescence in situ hybridization (T-FISH).". Cytogenet. Cell Genet. 87 (1-2): 132-3. PMID 10640833.
- Moloney DJ, Panin VM, Johnston SH, et al. (2000). "Fringe is a glycosyltransferase that modifies Notch.". Nature 406 (6794): 369-75. doi: . PMID 10935626.
- Shimizu K, Chiba S, Saito T, et al. (2001). "Manic fringe and lunatic fringe modify different sites of the Notch2 extracellular region, resulting in different signaling modulation.". J. Biol. Chem. 276 (28): 25753-8. doi: . PMID 11346656.
- Thélu J, Rossio P, Favier B (2003). "Notch signalling is linked to epidermal cell differentiation level in basal cell carcinoma, psoriasis and wound healing.". BMC Dermatol. 2: 7. PMID 11978185.
- Panin VM, Shao L, Lei L, et al. (2002). "Notch ligands are substrates for protein O-fucosyltransferase-1 and Fringe.". J. Biol. Chem. 277 (33): 29945-52. doi: . PMID 12036964.
- 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.
- Shao L, Moloney DJ, Haltiwanger R (2003). "Fringe modifies O-fucose on mouse Notch1 at epidermal growth factor-like repeats within the ligand-binding site and the Abruptex region.". J. Biol. Chem. 278 (10): 7775-82. doi: . PMID 12486116.
- Veeraraghavalu K, Pett M, Kumar RV, et al. (2004). "Papillomavirus-mediated neoplastic progression is associated with reciprocal changes in JAGGED1 and manic fringe expression linked to notch activation.". J. Virol. 78 (16): 8687-700. doi: . PMID 15280477.
- Collins JE, Wright CL, Edwards CA, et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome.". Genome Biol. 5 (10): R84. doi: . PMID 15461802.
- 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.