DLX3
This article may be too technical for most readers to understand. (June 2015) |
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Homeobox protein DLX-3 is a protein that in humans is encoded by the DLX3 gene.[1][2]
Function
[edit | edit source]Dlx3 is a crucial regulator of hair follicle differentiation and cycling. Dlx3 transcription is mediated through Wnt, and colocalization of Dlx3 with phospho-SMAD1/5/8 is involved in the regulation of transcription by BMP signaling.[3] Dlx3 transcription is also induced by BMP-2 through transactivation with SMAD1 and SMAD4.[4]
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17.[2]
Clinical significance
[edit | edit source]Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome (TDO) and amelogenesis imperfecta with taurodontism.[2]
References
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Further reading
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External links
[edit | edit source]- DLX3+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Overview of all the structural information available in the PDB for UniProt: O60479 (Homeobox protein DLX-3) at the PDBe-KB.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.