LOXL1
From Wikipedia, the free encyclopedia
Lysyl oxidase-like 1
|
||||||||||||||
Identifiers | ||||||||||||||
Symbol(s) | LOXL1; LOL; LOXL | |||||||||||||
External IDs | OMIM: 153456 MGI: 106096 HomoloGene: 4074 | |||||||||||||
|
||||||||||||||
RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 4016 | 16949 | ||||||||||||
Ensembl | ENSG00000129038 | ENSMUSG00000032334 | ||||||||||||
Uniprot | Q08397 | Q4QQJ7 | ||||||||||||
Refseq | XM_001133864 (mRNA) XP_001133864 (protein) |
NM_010729 (mRNA) NP_034859 (protein) |
||||||||||||
Location | Chr 15: 72.01 - 72.03 Mb | Chr 9: 58.09 - 58.11 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Lysyl oxidase-like 1, also known as LOXL1, is a human gene.[1]
This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family.[1]
[edit] References
[edit] Further reading
- Csiszar K (2001). "Lysyl oxidases: a novel multifunctional amine oxidase family.". Prog. Nucleic Acid Res. Mol. Biol. 70: 1–32. PMID 11642359.
- Kagan HM, Li W (2003). "Lysyl oxidase: properties, specificity, and biological roles inside and outside of the cell.". J. Cell. Biochem. 88 (4): 660–72. doi: . PMID 12577300.
- Molnar J, Fong KS, He QP, et al. (2003). "Structural and functional diversity of lysyl oxidase and the LOX-like proteins.". Biochim. Biophys. Acta 1647 (1-2): 220–4. PMID 12686136.
- Kenyon K, Modi WS, Contente S, Friedman RM (1993). "A novel human cDNA with a predicted protein similar to lysyl oxidase maps to chromosome 15q24-q25.". J. Biol. Chem. 268 (25): 18435–7. PMID 7689553.
- Kim Y, Boyd CD, Csiszar K (1995). "A new gene with sequence and structural similarity to the gene encoding human lysyl oxidase.". J. Biol. Chem. 270 (13): 7176–82. PMID 7706256.
- Goy A, Gilles F, Remache Y, Zelenetz AD (2000). "Physical linkage of the lysyl oxidase-like (LOXL1) gene to the PML gene on human chromosome 15q22.". Cytogenet. Cell Genet. 88 (1-2): 22–4. PMID 10773658.
- 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.
- Jung ST, Kim MS, Seo JY, et al. (2004). "Purification of enzymatically active human lysyl oxidase and lysyl oxidase-like protein from Escherichia coli inclusion bodies.". Protein Expr. Purif. 31 (2): 240–6. PMID 14550642.
- Liu X, Zhao Y, Gao J, et al. (2004). "Elastic fiber homeostasis requires lysyl oxidase-like 1 protein.". Nat. Genet. 36 (2): 178–82. doi: . PMID 14745449.
- Noblesse E, Cenizo V, Bouez C, et al. (2004). "Lysyl oxidase-like and lysyl oxidase are present in the dermis and epidermis of a skin equivalent and in human skin and are associated to elastic fibers.". J. Invest. Dermatol. 122 (3): 621–30. doi: . PMID 15086544.
- 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.
- Thomassin L, Werneck CC, Broekelmann TJ, et al. (2006). "The Pro-regions of lysyl oxidase and lysyl oxidase-like 1 are required for deposition onto elastic fibers.". J. Biol. Chem. 280 (52): 42848–55. doi: . PMID 16251195.
- Cenizo V, André V, Reymermier C, et al. (2007). "LOXL as a target to increase the elastin content in adult skin: a dill extract induces the LOXL gene expression.". Exp. Dermatol. 15 (8): 574–81. doi: . PMID 16842595.
- Thorleifsson G, Magnusson KP, Sulem P, et al. (2007). "Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.". Science 317 (5843): 1397–400. doi: . PMID 17690259.
- Damji KF (2007). "Progress in understanding pseudoexfoliation syndrome and pseudoexfoliation-associated glaucoma.". Can. J. Ophthalmol. 42 (5): 657–8. doi: . PMID 17891191.