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MSXs

Vertebrate Msx genes are unlinked, homeobox-containing genes that bear homology to the Drosophila muscle segment homeobox gene.

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MSX1 MSX2

- MSXs genes are expressed at multiple sites of tissue-tissue interactions during vertebrate embryonic development.

- Inductive interactions mediated by the MSXs genes are essential for normal craniofacial, limb and ectodermal organ morphogenesis, and are also essential to survival in mice, as manifested by the phenotypic abnormalities shown in knockout mice and in humans.

- The involvement of Msx homeobox genes (MSXs) in skull and tooth formation has received a great deal of attention. Recent studies also indicate a role for the msh/Msx gene family in development of the nervous system.

See also

- transcription factors
- neural-tissue organogenesis
- interactions of the Drosophila muscle segment homeobox (MSHs) gene with other homeobox genes
- repressive cascade that leads to neuroectoderm patterning
- MSXs genes in neural-crest induction
- patterning of the vertebrate neural tube
- diencephalon midline formation
- neurogenesis
- signalling molecules

  • BMPs

References

- Ramos C, Robert B. msh/Msx gene family in neural development. Trends Genet. 2005 Nov;21(11):624-32. PMID: #16169630#

- Alappat S, Zhang ZY, Chen YP. Msx homeobox gene family and craniofacial development. Cell Res. 2003 Dec;13(6):429-42. PMID: #14728799#

- Davidson, D. : The function and evolution of Msx genes: pointers and paradoxes. Trends Genet. 11: 405-411, 1995. PubMed ID : #7482767#