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Tankyrase, a Poly(ADP-Ribose) Polymerase at Human Telomeres

Science  20 Nov 1998:
Vol. 282, Issue 5393, pp. 1484-1487
DOI: 10.1126/science.282.5393.1484

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Abstract

Tankyrase, a protein with homology to ankyrins and to the catalytic domain of poly(adenosine diphosphate–ribose) polymerase (PARP), was identified and localized to human telomeres. Tankyrase binds to the telomeric protein TRF1 (telomeric repeat binding factor–1), a negative regulator of telomere length maintenance. Like ankyrins, tankyrase contains 24 ankyrin repeats in a domain responsible for its interaction with TRF1. Recombinant tankyrase was found to have PARP activity in vitro, with both TRF1 and tankyrase functioning as acceptors for adenosine diphosphate (ADP)–ribosylation. ADP-ribosylation of TRF1 diminished its ability to bind to telomeric DNA in vitro, suggesting that telomere function in human cells is regulated by poly(ADP-ribosyl)ation.

  • * Present address: European Molecular Biology Laboratory–Heidelberg, Meyerhofstrasse 1, D-69117, Heidelberg, Germany.

  • To whom correspondence should be addressed. E-mail: delange{at}rockvax.rockefeller.edu

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