Erratum to "Sealing the gap between nuclear DNA damage and longevity" [Mol. Cell. Endocrinol. 299 (2009) 112-117] (DOI:10.1016/j.mce.2008.10.031);Sealing the gap between nuclear DNA damage and longevity

Molecular and Cellular Endocrinology

Volumn 299, Issue 1, 2009, Pages 112-117

  Schumacher, Björn ^a   Hoeijmakers, Jan H ^a   Garinis, George A ^a  

^a INSTITUTE OF MOLECULAR BIOLOGY AND BIOTECHNOLOGY   (Greece)

Author keywords

DNA damage; Longevity; Progeria

Indexed keywords

CELL NUCLEUS DNA;

AGING; ARTICLE; DNA DAMAGE; DNA SYNTHESIS; EXCISION REPAIR; GENOME ANALYSIS; HUMAN; LONGEVITY; NEOPLASM; NONHUMAN; OXIDATIVE STRESS; PREMATURITY; PRIORITY JOURNAL;

EID: 58349112555     PISSN: 03037207     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mce.2009.02.003     Document Type: Erratum

References (37)

1. Andressoo J.O., Hoeijmakers J.H., and Mitchell J.R. Nucleotide excision repair disorders and the balance between cancer and aging. Cell Cycle 5 (2006) 2886-2888
2. Bartke A. Is growth hormone deficiency a beneficial adaptation to aging? Evidence from experimental animals. Trends Endocrinol Metab. 14 (2003) 340-344
3. Bartke A., and Brown-Borg H. Life extension in the dwarf mouse. Curr. Top. Dev. Biol. 63 (2004) 189-225
4. Beckman K.B., and Ames B.N. The free radical theory of aging matures. Physiol. Rev. 78 (1998) 547-581
5. Bootsma D., Kraemer K.H., Cleaver J.E., and Hoeijmakers J.H.J. Nucleotide excision repair syndromes: xeroderma pigmentosum, cockayne syndrome and trichothiodystrophy. In: Vogelstein B., and Kinzler K.W. (Eds). The Genetic Basis of Human Cancer (1998), McGraw-Hill, New York 245-274
6. Bootsma D., Cleaver K.H., and Hoeijmakers J.H.J. The Metabolic and Molecular Basis of Inherited Disease (2001), McGraw-Hill, New York
7. Bootsma D., Cleaver K.H., and Hoeijmakers J.H.J. Nucleotide Excision Repair Syndromes: Xeroderma Pigmentosum, Cockayne Syndrome and Trichthiodystrophy (2002), McGraw-Hill Medical Publishing Division, New York
8. Brown-Borg H.M. Hormonal regulation of aging and life span. Trends Endocrinol. Metab. 14 (2003) 151-153
9. Carter C.S., Ramsey M.M., Ingram R.L., Cashion A.B., Cefalu W.T., Wang Z.Q., and Sonntag W.E. Models of growth hormone and igf-1 deficiency: applications to studies of aging processes and life-span determination. J. Gerontol. A: Biol. Sci. Med. Sci. 57 (2002) B177-188
10. Carter C.S., Ramsey M.M., and Sonntag W.E. A critical analysis of the role of growth hormone and igf-1 in aging and lifespan. Trends Genet. 18 (2002) 295-301
11. Chandrashekar V., Zaczek D., and Bartke A. The consequences of altered somatotropic system on reproduction. Biol. Reprod. 71 (2004) 17-27
12. de Boer J., Andressoo J.O., de Wit J., Huijmans J., Beems R.B., van Steeg H., Weeda G., van der Horst G.T., van Leeuwen W., Themmen A.P., Meradji M., and Hoeijmakers J.H. Premature aging in mice deficient in DNA repair and transcription. Science 296 (2002) 1276-1279
13. de Boer J., Donker I., de Wit J., Hoeijmakers J.H., and Weeda G. Disruption of the mouse xeroderma pigmentosum group d DNA repair/basal transcription gene results in preimplantation lethality. Cancer Res. 58 (1998) 89-94
14. de Boer J., and Hoeijmakers J.H. Nucleotide excision repair and human syndromes. Carcinogenesis 21 (2000) 453-460
15. de Laat W.L., Jaspers N.G., and Hoeijmakers J.H. Molecular mechanism of nucleotide excision repair. Genes Dev. 13 (1999) 768-785
16. Friedberg E., Walker G., and Siede W. DNA Repair and Mutagenesis (1995), American Society of Microbiology Press, Washington
17. Garinis G.A., Jans J., and van der Horst G.T. Photolyases: capturing the light to battle skin cancer. Future Oncol. 2 (2006) 191-199
18. Garinis G.A., Mitchell J.R., Moorhouse M.J., Hanada K., de Waard H., Vandeputte D., Jans J., Brand K., Smid M., van der Spek P.J., Hoeijmakers J.H., Kanaar R., and van der Horst G.T. Transcriptome analysis reveals cyclobutane pyrimidine dimers as a major source of UV-induced DNA breaks. EMBO J. 24 (2005) 3952-3962
19. Giglia-Mari G., Coin F., Ranish J.A., Hoogstraten D., Theil A., Wijgers N., Jaspers N.G., Raams A., Argentini M., van der Spek P.J., Botta E., Stefanini M., Egly J.M., Aebersold R., Hoeijmakers J.H., and Vermeulen W. A new, tenth subunit of fifth is responsible for the DNA repair syndrome trichothiodystrophy group a. Nat. Genet. 36 (2004) 714-719
20. Gorgels T.G., van der Pluijm I., Brandt R.M., Garinis G.A., van Steeg H., van den Aardweg G., Jansen G.H., Ruijter J.M., Bergen A.A., van Norren D., Hoeijmakers J.H., and van der Horst G.T. Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for cockayne syndrome. Mol. Cell Biol. 27 (2007) 1433-1441
21. Hasty P., Campisi J., Hoeijmakers J., van Steeg H., and Vijg J. Aging and genome maintenance: lessons from the mouse?. Science 299 (2003) 1355-1359
22. Hoeijmakers J.H. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies. Eur. J. Cancer. 30A (1994) 1912-1921
23. Hoeijmakers J.H. Genome maintenance mechanisms for preventing cancer. Nature 411 (2001) 366-374
24. Hoeijmakers J.H. Genome maintenance mechanisms are critical for preventing cancer as well as other aging-associated diseases. Mech. Ageing Dev. 128 (2007) 460-462
25. Jans J., Garinis G.A., Schul W., van Oudenaren A., Moorhouse M., Smid M., Sert Y.G., van der Velde A., Rijksen Y., de Gruijl F.R., van der Spek P.J., Yasui A., Hoeijmakers J.H., Leenen P.J., and van der Horst G.T. Differential role of basal keratinocytes in UV-induced immunosuppression and skin cancer. Mol. Cell Biol. 26 (2006) 8515-8526
26. Jaspers N.G., Raams A., Silengo M.C., Wijgers N., Niedernhofer L.J., Robinson A.R., Giglia-Mari G., Hoogstraten D., Kleijer W.J., Hoeijmakers J.H., and Vermeulen W. First reported patient with human ercc1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure. Am. J. Hum. Genet. 80 (2007) 457-466
27. Longo V.D., and Finch C.E. Evolutionary medicine: from dwarf model systems to healthy centenarians?. Science 299 (2003) 1342-1346
28. Martin G.M. Genetic modulation of senescent phenotypes in homo sapiens. Cell 120 (2005) 523-532
29. Mitchell J.R., Hoeijmakers J.H., and Niedernhofer L.J. Divide and conquer: nucleotide excision repair battles cancer and ageing. Curr. Opin. Cell Biol. 15 (2003) 232-240
30. Nance M.A., and Berry S.A. Cockayne syndrome: review of 140 cases. Am. J. Med. Genet. 42 (1992) 68-84
31. Niedernhofer L.J., Garinis G.A., Raams A., Lalai A.S., Robinson A.R., Appeldoorn E., Odijk H., Oostendorp R., Ahmad A., van Leeuwen W., Theil A.F., Vermeulen W., van der Horst G.T., Meinecke P., Kleijer W.J., Vijg J., Jaspers N.G., and Hoeijmakers J.H. A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis. Nature 444 (2006) 1038-1043
32. Schumacher B., van der Pluijm I., Moorhouse M.J., Kosteas T., Robinson A.R., Suh Y., Breit T.M., van Steeg H., Niedernhofer L.J., van Ijcken W., Bartke A., Spindler S.R., Hoeijmakers J.H., van der Horst G.T., and Garinis G.A. Delayed and accelerated aging share common longevity assurance mechanisms. PLoS Genet. 4 8 (2008) e1000161
33. van der Horst G.T., Meira L., Gorgels T.G., de Wit J., Velasco-Miguel S., Richardson J.A., Kamp Y., Vreeswijk M.P., Smit B., Bootsma D., Hoeijmakers J.H., and Friedberg E.C. Uvb radiation-induced cancer predisposition in cockayne syndrome group a (csa) mutant mice. DNA Rep. (Amst.) 1 (2002) 143-157
34. van der Horst G.T., van Steeg H., Berg R.J., van Gool A.J., de Wit J., Weeda G., Morreau H., Beems R.B., van Kreijl C.F., de Gruijl F.R., Bootsma D., and Hoeijmakers J.H. Defective transcription-coupled repair in cockayne syndrome b mice is associated with skin cancer predisposition. Cell 89 (1997) 425-435
35. van der Pluijm I., Garinis G.A., Brandt R.M., Gorgels T.G., Wijnhoven S.W., Diderich K.E., de Wit J., Mitchell J.R., van Oostrom C., Beems R., Niedernhofer L.J., Velasco S., Friedberg E.C., Tanaka K., van Steeg H., Hoeijmakers J.H., and van der Horst G.T. Impaired genome maintenance suppresses the growth hormone-insulin-like growth factor 1 axis in mice with cockayne syndrome. PLoS Biol. 5 (2006) e2
36. Vijg J. Somatic mutations and aging: a re-evaluation. Mutat. Res. 447 (2000) 117-135
37. Wood R.D. DNA repair in eukaryotes. Annu. Rev. Biochem. 65 (1996) 135-167