Protein of life, protein of death The same enzyme regulates programmed cell death and embryonic
development By Andrea Rinaldi
Complex, multicellular organisms must finely regulate their inner environment to assure cells can
thrive, but must also initiate apoptosis (programmed cell death) when necessary. Apoptosis is
critical for normal development and tissue homeostasis, and aberrant apoptosis can lead to cancer
and neural degeneration. In a PNAS article published online December 8, Jianhua Zhang and colleagues
at the University of Cincinnati College of Medicine pinpoint an enzyme that plays an important role
in both the regulation of normal apoptosis and embryogenesis in mammals (PNAS,
DOI:10.1073/pnas.2636393100, December 8, 2003).
Zhang et al. investigated the in vivo function of endonuclease G (EndoG), a mitochondrial protein
encoded in the nucleus, previously reported to be important for nuclear DNA fragmentation during
apoptosis and mitochondrial DNA replication. The authors studied the consequences of EndoG
deficiency in mice and observed that homozygous mutant embryos died early during development and had
lost normal morphology, while heterozygous animals developed normally. Mitochondrial numbers were
the same in mutant and wildtype mice, suggesting that EndoG is not involved in mitochondrial DNA
replication. The authors also observed that EndoG mutant cells subjected to apoptotic stimuli were
more resistant to cell death than wildtype control cells.
Read the rest at The Scientis.com biomedcentral.com02Open ↗
Posted by Robert Karl Stonjek.