The functioning of the vertebrate heart depends upon the proper organi
zation of its complex structure: atrial and ventricular myocytes, the
conduction system, the fibrous skeleton that forms the chambers and va
lves of the heart, the coronary vessels, and neural elements. Cell-typ
e specific transgenic models for addressing molecular mechanisms regul
ating heart development necessitate controllable gene insertions into
the precursors of each cell type forming the heart. The unique propert
ies of retrovirus-based shuttle vectors provide a powerful tool for (a
) identifying the origin and lineage relationships of all cell types f
orming the heart; and (b) gene targeting to the selected cell type and
time point during heart development.