WNT6
| wingless-type MMTV integration site family, member 6 | |
|---|---|
| Identifiers | |
| Symbol | WNT6 |
| Entrez | 7475 |
| HUGO | 12785 |
| OMIM | 604663 |
| RefSeq | NM_006522 |
| UniProt | Q9Y6F9 |
| Other data | |
| Locus | Chr. 2 q35 |
Wingless-type MMTV integration site family, member 6, also known as WNT6, is a human gene.[1][2]
The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family, which are involved in the Wnt signaling pathway. It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line.[3] The gene overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome 2q35 region. The protein encoded by this gene is 97% identical to the mouse Wnt6 protein at the amino acid level.[1]
Role in Development
Wnt6 plays a role in the formation and maturation of different embryonic structures, namely the fetal heart, ventral body wall, and somite derived structures. Wnt6, through the canonical Wnt signaling pathway, inhibits the induction of cardiogenic mesoderm.[4] For this reason, Wnt6 inhibitors like Cerberus must be present to allow the cells to be induced.[4] Knockout models show that without Wnt6 the fetus develops an enlarged heart, while upregulating Wnt6 results in the heart being underdeveloped.[4] Several Wnts, including Wnt6, have shown to be involved in the formation of the ventral body wall and when inhibited result in birth defects such as failure of the wall to close, hypoplasia of the musculature, and other defects.[5] Following the formation of the somites from the Paraxial Mesoderm, the outermost cells of the somites undergo a mesenchymal to epithelial transition.[6] Wnt6 is expressed by the overlying ectoderm and promotes the production of Paraxis, which facilitates the transition.[6] While many structures will still form if Wnt6 is knocked out, the structures (ribs, vertebra, and muscles) are fused and not organized properly.[6] On the other hand, if Wnt6 is upregulated, muscle in the limbs and surrounding areas are decreased as the mesenchymal progenitor cells that migrate and become the muscle are locked in the somite as epithelial cells.[6]
References
- 1 2 "Entrez Gene: WNT2 wingless-type MMTV integration site family, member 2".
- ↑ Rankin J, Strachan T, Lako M, Lindsay S (1999). "Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization". Cytogenet. Cell Genet. 84 (1–2): 50–2. doi:10.1159/000015212. PMID 10343101.
- ↑ Kirikoshi H, Sekihara H, Katoh M (May 2001). "WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells". Biochem. Biophys. Res. Commun. 283 (4): 798–805. doi:10.1006/bbrc.2001.4855. PMID 11350055.
- 1 2 3 Lavery, Danielle L.; Martin, Jennifer; Turnbull, Yvonne D.; Hoppler, Stefan (November 2008). "Wnt6 signaling regulates heart muscle development during organogenesis". Developmental Biology 323 (2): 177–188. doi:10.1016/j.ydbio.2008.08.032.
- ↑ Zhang, Lingling; Li, Hanjun; Yu, Jian; Cao, Jingjing; Chen, Huihui; Zhao, Haixia (March 2014). "Ectodermal Wnt signaling regulates abdominal myogenesis during ventral body wall development". Developmental Biology 387 (1): 64–72. doi:10.1016/j.ydbio.2013.12.027.
- 1 2 3 4 Schmidt, Corina; Stoeckelhuber, Mechthild; McKinnell, Iain; Putz, Reinhard; Christ, Bodo; Patel, Ketan (July 2004). "Wnt 6 regulates the epithelialisation process of the segmental plate mesoderm leading to somite formation". Developmental Biology 271 (1): 198–209. doi:10.1016/j.ydbio.2004.03.016.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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