X-Message-Number: 28998
Date: Sun, 21 Jan 2007 10:27:22 -0500
From: Keith Henson <>
Subject: Re: New syndrome reconciles theories of ageing

[Again, not promoting any theory, just thought this might be of interest 
here.  KH]

Nature Reviews Genetics 8, 90 (February 2007) | doi:10.1038/nrg2050
Human genetics: New syndrome reconciles theories of ageing
Patrick Goymer

Is ageing merely the result of the accumulation of cellular damage over 
time, or is it genetically regulated? A new premature-ageing syndrome and a 
comparison of the transcriptomes of naturally and prematurely aged mice 
reconcile these two theories. They indicate the existence of a programmed 
response to DNA damage accumulation that is mediated by the insulin-like 
growth factor (IGF) pathway and is associated with ageing.

Mutations in components of the nucleotide excision repair (NER) pathway can 
cause either premature ageing or cancer susceptibility. Premature ageing 
arises from mutations that affect the repair of lesions that block 
transcription; cancer susceptibility is caused by mutations that affect 
genome-wide mutation prevention, irrespective of transcription. The authors 
have identified a new syndrome XPF-ERCC1 progeria (XFE) that combines both 
phenotypes. XPF-ERCC1 is a two-subunit endonuclease that is required for 
NER. Patients with mild mutations in XPF have xeroderma pigmentosum, a 
cancer-susceptibility syndrome. However, a patient with a severe mutation 
in a highly conserved residue of the same gene also shows premature ageing.

To investigate further, the authors created a mouse model of this syndrome 
an Ercc1-null strain. They compared the liver and kidney transcriptomes of 
young mutant mice with naturally aged wild-type mice, and also wild-type 
mice that were subjected to a genotoxic stress. All three showed similar 
differences in gene expression to the controls: growth-promoting hormones, 
especially those in the IGF pathway, were downregulated, whereas DNA 
repair, anti-oxidant defence, glucose storage and apoptosis were upregulated.

The authors propose that increased DNA damage, as a result of natural 
ageing, environmental insult or genetic deficiency, triggers a switch from 
growth to repair and the prolonging of life. This is consistent with the 
effects of mutations in IGF pathway components and reduced oxidative damage 
through caloric restriction, both of which prolong life. This link between 
DNA repair and ageing shows that damage accumulation does cause ageing, but 
that its progress is tightly regulated by the IGF pathway and repair 
capacity. The next step is to elucidate the mechanism by which IGF does this.

References and links
ORIGINAL RESEARCH PAPER
1.. Niedernhofer, L. J. et al. A new progeroid syndrome reveals that 
genotoxic stress suppresses the somatotroph axis. Nature 444, 1038-1044 (2006)
a.. Article
b.. PubMed
c.. ChemPort
FURTHER READING
1.. Capell, B. C. & Collins, F. S. Human laminopathies: nuclei gone 
genetically awry. Nature Rev. Genet. 7, 940-952 (2006)
a.. Article
2.. Christensen, K., Johnson, T. E. & Vaupel, J. W. The quest for genetic 
determinants of human longevity: challenges and insights. Nature Rev. 
Genet. 7, 436-448 (2006)
a.. Article
3.. Longo, V. D., Mitteldorf, J. & Skulachev, V. P. Programmed and 
altruistic ageing. Nature Rev. Genet. 6, 866-872 (2005)
a.. Article
Source: Nature
http://www.nature.com/nrg/journal/v8/n2/full/nrg2050.html

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