Diatom cells are encased within a silica-based cell wall (frustule) that se
rves as armour-like protection for the enclosed protoplast. Maintaining the
integrity of the frustule requires a precise coupling between the biogenes
is of new frustule components and the cell cycle. Thus far, the molecular m
echanisms by which this coupling is achieved are unknown. This study demons
trates that pleuralins (formerly HEPs), a previously characterized family o
f diatom cell wall proteins, are involved in cell cycle-dependent frustule
development, The frustule is made up of two, overlapping half-shells termed
the epitheca and hypotheca. Both thecae are morphologically identical, yet
immunolocalisation with anti-pleuralin antibodies demonstrates that their
protein composition is clearly different. During interphase, pleuralins are
associated only with the epitheca, where they are confined to the inner su
rface of the terminal elements (pleural bands) in the region of overlap wit
h the hypotheca. At cell division, pleuralins also become associated with t
he newly formed pleural bands of the hypotheca, Remarkably, this process is
concomitant with the functional conversion of the parental hypotheca into
the epitheca of one of the progeny cells. These results indicate that devel
opmentally controlled association of pleuralins with the frustule is involv
ed in hypotheca-epitheca differentiation, which is a crucial process to ens
ure proper frustule development.