In: Biology
Based on your understanding of sea urchin and fruit fly gastrulation, would you expect the ventral furrowing of the fruit fly to require an epithelial-to-mesenchymal transition? Why or why not?
Yes, a ventral furrow is formed in fruitfly during gastrulation.
At the time of midblastula transition, gastrulation begins. The first movements of Drosophila gastrulation segregate the presumptive mesoderm, endoderm, and ectoderm. The prospective mesoderm—about 1000 cells constituting the ventral midline of the embryo—folds inward to produce the ventral furrow. This furrow eventually pinches off from the surface to become a ventral tube within the embryo. It then flattens to form a layer of mesodermal tissue beneath the ventral ectoderm. The prospective endoderm invaginates as two pockets at the anterior and posterior ends of the ventral furrow. The pole cells are internalized along with the endoderm. At this time, the embryo bends to form the cephalic furrow.
The ectodermal cells on the surface and the mesoderm undergo convergence and extension, migrating toward the ventral midline to form the germ band, a collection of cells along the ventral midline that includes all the cells that will form the trunk of the embryo. The germ band extends posteriorly and, perhaps because of the egg case, wraps around the top (dorsal) surface of the embryo. Thus, at the end of germ band formation, the cells destined to form the most posterior larval structures are located immediately behind the future head region. At this time, the body segments begin to appear, dividing the ectoderm and mesoderm. The germ band then retracts, placing the presumptive posterior segments into the posterior tip of the embryo.
While the germ band is in its extended position, several key morphogenetic processes occur organogenesis, segmentation, and the segregation of the imaginal discs. In addition, the nervous system forms from two regions of ventral ectoderm. Neuroblasts differentiate from this neurogenic ectoderm within each segment (and also from the nonsegmented region of the head ectoderm). Therefore, in insects like Drosophila, the nervous system is located ventrally, rather than being derived from a dorsal neural tube as in vertebrates.
The general body plan of Drosophila is the same in the embryo, the larva, and the adult, each of which has a distinct head end and a distinct tail end, between which are repeating segmental units. Three of these segments form the thorax, while another eight segments form the abdomen. Each segment of the adult fly has its own identity. The first thoracic segment, for example, has only legs; the second thoracic segment has legs and wings; and the third thoracic segment has legs and halteres (balancers). Thoracic and abdominal segments can also be distinguished from each other by differences in the cuticle.