Because fungal cell walls are shaped during construction, factors that
regulate wall biogenesis must play a decisive role in morphogenesis.
By delivering ingredients for wall formation in vesicles, fungi have a
de facto mechanism to mold their own shape. The gradients in wall for
mation required for cell morphogenesis ensue from the pattern of vesic
le discharge. A vesicle-based, mathematical model of fungal morphogene
sis revealed that a relatively simple process could establish these gr
adients. The model and its underlying hyphoid equation assumes that wa
ll-building vesicles emanate from a vesicle supply center (VSC). The V
SC serves as an organizing center from which vesicles would move radia
lly to the cell surface in all directions at random. VSC displacement
is then an immediate cause of morphogenesis: a sustained linear displa
cement of the VSC would generate a polarized pattern of exocytosis req
uired to make a hypha. The model predicts that the Spitzenkorper funct
ions as a VSC. We have tested this prediction by analyzing instances w
here dislocations in Spitzenkorper position result in hyphal deformati
ons. When the VSC was programmed to duplicate the movements of the Spi
tzenkorper before, during, and after a deformation, the resulting shap
es mimicked closely the observed deformations. These correlations supp
ort the contention that the position and movement of the VSC determine
s the morphology of the fungal cell wall. The computer model has been
refined to incorporate transverse random oscillations of the VSC to si
mulate more realistically the meandering shape of fungal hyphae. The m
odel predicts that hyphal ring formation results from a sustained dire
ctional bias to the transverse oscillations of the Spitzenkorper.