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GENES & DEVELOPMENT 18:1781-1799, 2004
©2004 by Cold Spring Harbor Laboratory Press; ISSN 0890-9369/ $5.00
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REVIEW

Functional links between telomeres and proteins of the DNA-damage response

Fabrizio d'Adda di Fagagna1,3,4, Soo-Hwang Teo2,3 and Stephen P. Jackson2,5

1 IFOM Foundation—The FIRC Institute of Molecular Oncology Foundation, 20139 Milan, Italy; 2 The Wellcome Trust and Cancer Research UK Gurdon Institute, and Department of Zoology, University of Cambridge, Cambridge CB2 1QR, UK

In response to DNA damage, cells engage a complex set of events that together comprise the DNA-damage response (DDR). These events bring about the repair of the damage and also slow down or halt cell cycle progression until the damage has been removed. In stark contrast, the ends of linear chromosomes, telomeres, are generally not perceived as DNA damage by the cell even though they terminate the DNA double-helix. Nevertheless, it has become clear over the past few years that many proteins involved in the DDR, particularly those involved in responding to DNA double-strand breaks, also play key roles in telomere maintenance. In this review, we discuss the current knowledge of both the telomere and the DDR, and then propose an integrated model for the events associated with the metabolism of DNA ends in these two distinct physiological contexts.

[Keywords: Telomere; DNA-damage response; checkpoint; senescence; DNA repair]


Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1214504.

3 These authors contributed equally to this work.

Corresponding authors:

4 E-MAIL dadda{at}ifom-firc.it; FAX 39-02-574303-231.

5 E-MAIL s.jackson{at}gurdon.cam.ac.uk; FAX 44-1223-334089.


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