Vertebrate tinman homologues and cardiac differentiation.

In Drosophila, the homeobox gene tinman is required for specification of dorsal vessel and a number of mesodermal subtypes. Six tinman homologues have now been found in diverse vertebrate species: Nkx2-3, 2-5, 2-6, 2-7, 2-8 and 2-9. Of these, Nkx2-5 appears to be the mostly highly conserved among species, in terms of both primary protein sequence and mRNA expression pattern. Of the others, some have been found as yet only in a single species. Although expression patterns of vertebrate tinman homologues indicate that they may play a role in the specification of several mesodermal or endodermal tissues, to date most attention have been focussed on their role in cardiac development. Results of these studies indicate that, as for Drosophila tinman, vertebrate tinman homologues may be required for heart formation, but may not be sufficient. Studies in Drosophila are defining other pathways which are required in concert with tinman for dorsal vessel formation. Circumstantial evidence suggests that similar pathways may be operative in vertebrate heart formation. This review summarizes recent advances in our understanding of vertebrate tinman homologues and interacting genetic pathways.     

Phenotypic characterization of the murine Nkx2.6 homeobox gene by gene targeting

The NK-2 homeobox genes have been shown to play critical roles in the development of specific organs and tissues. Nkx2.6 is a member of the NK-2 homeobox gene family and is most closely related to the Drosophila tinman gene. Nkx2.6 is expressed in the caudal pharyngeal pouches, the caudal heart progenitors, the sinus venosus, and the outflow tract of the heart and in a short segment of the gut at early stages of embryogenesis. To investigate the function of Nkx2.6 in vivo, we generated mice with null mutations of Nkx2.6 by the gene targeting technique. Homozygous Nkx2.6 mutant mice were viable and fertile. There were no obvious abnormalities in the caudal pharyngeal pouch derivatives (the thymus, parathyroid glands, and thyroid gland), heart, and gut. Expression of Nkx2.6 overlaps that of Nkx2.5 in the pharynx and heart and that of Nkx2.3 in the pharynx. Interestingly, in mutant embryos homozygous for Nkx2.6, Nkx2.5 expression extended to the lateral side of the pharynx, suggesting a compensatory function of Nkx2.5 in the mutant pharyngeal pouches.