Embryonic shape and form is driven by the physical mechanics of component cells
and tissues. Genes and signaling networks may control the protein composition of
cells but it is the forces generated by cells and their interactions with their
surroundings that dictate the form of the resulting embryo and the survival of the
larva. We are applying basic principles of experimental biophysics and
developmental biology to investigate the roles of such forces and tissue
biomechanics in early development. Our first efforts have revealed cryptic changes
in biomechanical properties of developing amphibian embryos and the
spatiotemporal variation of these properties at the cellular and organismal scale.
Using molecular perturbations we have begun a systematic analysis of the roles of
cell- and tissue-structural proteins in establishing "passive" material properties and
"active" force-generating programs in key tissues that drive embryos from spherical
balls of cells to elongate tadpoles. Interestingly, tissues at the earliest stages of
embryonic development are ultra-soft (< 100 Pa) and are shaped principally by the
action of the actomyosin cytoskeleton. We will discuss how observations from these
studies are driving development of new theories of morphogenesis incorporating
both cell signaling and mechanical feedback and the development of new
experimental tools to test them.