PARP CLEAVAGE IN THE APOPTOTIC PATHWAY IN S2 CELLS FROM DROSOPHILA-MELANOGASTER
Citation
P. Poltronieri et al., PARP CLEAVAGE IN THE APOPTOTIC PATHWAY IN S2 CELLS FROM DROSOPHILA-MELANOGASTER, Biochemistry and cell biology, 75(4), 1997, pp. 445-449
Categorie Soggetti
Biology,"Cell Biology
SICI code
0829-8211(1997)75:4<445:PCITAP>2.0.ZU;2-T
Abstract
Caspase activities and two cDNA sequences have been identified in Dros
ophila melanogaster. To study the molecular events following the activ
ation of the apoptotic pathway in D. melanogaster, S2 cells were treat
ed with etoposide and the timing of the apoptotic events, such as casp
ase activation, mitochondrial pore opening, and loss of membrane asymm
etry, was determined. Poly(ADP-ribose) polymerase (PARP) is known to b
e cleaved in the early phase of apoptosis in vertebrate systems. Littl
e is known about the involvement of PARP cleavage in apoptosis in inve
rtebrates. If PARP inactivation is a general event, this could mean th
at DNA repair enzymes need to be cleaved for the death pathway to be c
ompleted. We have found that in etoposide treated cells, PARP protein
is processed, but the nature of the cleavage is not known. Further exp
eriments must be conducted and the peptide fragments must be sequenced
to relate protease activities with PARP cleavage.