Shelterin/telosome is a multi-protein complex at mammalian telomeres,
anchored to the double-stranded region by the telomeric-repeat binding
factors-1 and -2. In vitro modification of these proteins by poly(ADP-
ribosyl)ation through poly(ADP-ribose) polymerases-5 (tankyrases) and
-1/-2, respectively, impairs binding. Thereafter, at least telomeric-
repeat binding factor-1 is degraded by the proteasome. We show that
pharmacological inhibition of poly(ADP-ribose) polymerase activity in
cells from two different species leads to rapid decrease in median
telomere length and stabilization at a lower setting. Specific
knockdown of poly(ADP-ribose) polymerase-1 by RNA interference had the
same effect. The length of the single-stranded telomeric overhang as
well as telomerase activity were not affected. Release of inhibition
led to a fast re-gain in telomere length to control levels in cells
expressing active telomerase. We conclude that poly(ADP-ribose)
polymerase-1 activity and probably its interplay with telomeric-repeat
binding factor-2 is an important determinant in telomere regulation.
Our findings reinforce the link between poly(ADP-ribosyl)ation and
aging/longevity and also impact on the use of poly(ADP-ribose)
polymerase inhibitors in tumor therapy.
PMID: 18835851 [PubMed - as supplied by publisher]