Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos

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Abstract

Fermitin genes are highly conserved and encode cytocortex proteins that mediate integrin signalling. Fermitin 1 (Kindlin1) is implicated in Kindler syndrome, a human skin blistering disorder. We report the isolation of the three Fermitin orthologs from Xenopus laevis embryos and describe their developmental expression patterns. Fermitin 1 is expressed in the skin, otic and olfactory placodes, pharyngeal arches, pronephric duct, and heart. Fermitin 2 is restricted to the somites and neural crest. Fermitin 3 is expressed in the notochord, central nervous system, cement gland, ventral blood islands, vitelline veins, and myeloid cells. Our findings are consistent with the view that Fermitin 1 is generally expressed in the skin, Fermitin 2 in muscle, and Fermitin 3 in hematopoietic lineages. Moreover, we describe novel sites of Fermitin gene expression that extend our knowledge of this family. Our data provide a basis for further functional analysis of the Fermitin family in Xenopus laevis. © 2011 Wiley-Liss, Inc.

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Canning, C. A., Chan, J. S. K., Common, J. E. A., Lane, E. B., & Jones, C. M. (2011). Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos. Developmental Dynamics, 240(8), 1958–1963. https://doi.org/10.1002/dvdy.22683

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