During Drosophila metamorphosis, larval tissues, such as the salivary gland
s, are histolysed whereas imaginal tissues differentiate into adult structu
res forming at eclosion a fly-shaped adult. Inactivation of the lethal(2)gi
ant larvae (I(2)gl) gene encoding the cytoskeletal associated p127 protein,
causes malignant transformation of brain neuroblasts and imaginal disc cel
ls with developmental arrest at the larval-pupal transition phase. At this
stage, p127 is expressed in wildtype salivary glands which become fully his
tolysed 12-13 h after pupariation. By contrast to wild-type, administration
of 20-hydroxyecdsone to I(2)gl-deficient salivary glands is unable to indu
ce histolysis, although it releases stored glue granules and gives rise to
a nearly normal pupariation chromosome puffing, indicating that p127 is req
uired for salivary gland apoptosis, To unravel the I(2)gl function in this
tissue we used transgenic lines expressing reduced (similar to 0.1) or incr
eased levels of p127 (3.0). Here we show that the timing of salivary gland
histolysis displays an I(2)gl-dose response. Reduced p127 expression delays
histolysis whereas overexpression accelerates this process without affecti
ng the duration of third larval instar, prepupal and pupal development. Sim
ilar I(2)gl-dependence is noticed in the timing of expression of the cell d
eath genes reaper, head involution defective and grim, supporting the idea
that p127 plays a critical role in the implementation of ecdysone-triggered
apoptosis, These experiments show also that the timing of salivary gland a
poptosis can be manipulated without affecting normal development and provid
e ways to investigate the nature of the components specifically involved in
the apoptotic pathway of the salivary glands.