To understand the role of the spectrin-based membrane skeleton in gene
rating epithelial polarity, we characterized the distribution of membr
ane skeletal components in Drosophila ovarian follicle cells and in so
matic clones of mutant cells that lack alpha-spectrin. Immunolocalizat
ion data reveal that wild-type follicle cells contain two populations
of spectrin heterodimers: a network of alpha beta heterodimers concent
rated on the lateral plasma membrane and an alpha beta(H) population t
argeted to the apical surface. Induction of somatic clones lacking alp
ha-spectrin leads to follicle cell hyperplasia. Surprisingly, eliminat
ion of alpha-spectrin from follicle cells does not appear to prevent t
he assembly of conventional beta-spectrin and ankyrin at the lateral d
omain of the follicle cell plasma membrane, However, the alpha-subunit
is essential for the correct localization of beta(H)-spectrin to the
apical surface, As a consequence of disrupting the apical membrane ske
leton a distinct sub population of follicle cells undergoes unregulate
d proliferation which leads to the loss of monolayer organization and
disruption of the anterior-posterior axis of the oocyte. These results
suggest that the spectrin-based membrane skeleton is required in a de
velopmental pathway that controls follicle cell monolayer integrity an
d proliferation.