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ATM, telomeres and aging

Jonathan Weitzman

Genome Biology 2003, 4:spotlight-20030124-01  doi:10.1186/gb-spotlight-20030124-01

The electronic version of this article is the complete one and can be found online at:


Published:24 January 2003

© 2003 BioMed Central Ltd

Research news

ATM, the product of the gene mutated in ataxia-telangiectasia (A-T), is involved in the cellular response to DNA damage and has been implicated in telomere maintenance. Atm mutant mice display modest aging and growth retardation defects compared to A-T patients. In an Advanced Online Publication in Nature Wong et al. describe studies in mice to assess the interaction between ATM and telomeres (Nature, 22 January 2003, DOI:10.1038/nature01385). They bred Atm-deficient mice with animals lacking the telomerase RNA component (Terc). Double knockout mice showed an increase in genomic instability and chromosomal fusions, and premature lethality. Cell proliferation defects were also observed in primary cells in culture and in several stem-cell populations in vivo. The interaction between telomeres and ATM, and the impaired stem-cell reserve, explains the multi-organ affects in A-T patients.

References

  1. ATM: genome stability, neuronal development, and cancer cross paths.

    PubMed Abstract OpenURL

  2. [http://www.nature.com] webcite

    Nature