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Mol Cell Endocrinol. 2009 Feb 5;299(1):112-7. doi: 10.1016/j.mce.2008.10.031. Epub 2008 Nov 5.

Sealing the gap between nuclear DNA damage and longevity.

Author information

1
Department of Genetics, Centre for Biomedical Genetics, Erasmus University Medical Centre, PO Box 2040, 3000 CA Rotterdam, The Netherlands. [corrected]

Erratum in

  • Mol Cell Endocrinol. 2009 May 6;303(1-2):107.

Abstract

A number of progeroid syndromes with defects in the cellular response to DNA damage suggest that progressive genome instability represents an important aspect of the aging process. Here, we review a number of mouse models for progeroid syndromes that are caused by inherited defects in nucleotide excision repair and are characterized by rapid onset of aging symptoms and premature death. We argue that alterations in genome maintenance pathways impact complex physiological processes that may affect the onset of clinically defined age-related pathologies, including cancer as well as pathways that are normally associated with longevity.

PMID:
19027821
DOI:
10.1016/j.mce.2008.10.031
[Indexed for MEDLINE]

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