Abstract
THE instability of chromosomes with breaks induced by X-irradi-ation led to the proposal that the natural ends of chromosomes are capped by a specialized structure, the telomere1. Telomeres prevent end-to-end fusions and exonucleolytic degradation, enable the end of the linear DNA molecule to replicate, and function in cell division (reviewed in ref. 2). Human telomeric DNA comprises ˜2–20 kilobases (kb) of the tandemly repeated sequence (TTAGGG)n oriented 5′→3′ towards the end of the chromosome3,4, interspersed with variant repeats in the proximal region5. Immediately subtelomeric lie families of unrelated repeat motifs (telomere-associated sequences) whose function, if any, is unknown6,7. In lower eukaryotes the formation and maintenance of telomeres may be mediated enzymatically (by telomerase)8 or by recombination9; in man the mechanisms are poorly understood, although telomerase has been identified in HeLa cells4. Here we describe an a thalassaemia10 mutation associated with terminal truncation of the short arm of chromosome 16 (within band 16pl3.3) to a site 50 kb distal to the α globin genes, and show that (TTAGGG)n has been added directly to the site of the break. The mutation is stably inherited, proving that telomeric DNA alone is sufficient to stabilize the broken chromosome end. This mechanism may occur in any genetic disease associated with chromosome truncation.
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References
Muller, H. J. Collect. Net. 13, 182–193 (1938).
Zakian, V. A. A. Rev. Genet. 23, 579–604 (1989).
Moyzis, R. K. et al. Proc. natn. Acad. Sci. U.S.A. 85, 6622–6626 (1988).
Morin, G. B. Cell 59, 521–529 (1989).
Allshire, R. C., Dempster, M. & Hastie, N. D. Nucleic Acids Res. 17, 4611–4627 (1989).
Cheng, J.-F., Smith, C. L. & Cantor, C. R. Nucleic Acids Res. 17, 6109–6127 (1989).
de Lange, T. et al. Molec. cell. Biol 10, 518–527 (1990).
Yu, G.-L., Bradley, J. D., Attardi, L. D. & Blackburn, E. H. Nature 344, 126–132 (1990).
Wang, S.-S. & Zakian, V. A. Nature 345, 456–458 (1990).
Higgs, D. R. et al. Blood 73, 1081–1104 (1989).
Galanello, R., Paglietti, E., Melis, M. A., Giagu, L. & Cao, A. Acta Haematol. Basel 72, 34–36 (1984).
Yao, M.-C. & Yao, C.-H. Proc. natn. Acad. Sci. U.S.A. 78, 7436–7439 (1981).
Gusella, J. F. et al. Nature 318, 75–78 (1985).
Ledbetter, D. H. et al. Proc. natn. Acad. Sci. U.S.A. 86, 5136–5140 (1989).
Harris, P. C., Barton, N. J., Higgs, D. R., Reeders, S. T. & Wilkie, A. O. M. Genomics 7, 195–206 (1990).
Wilkie, A. O. M. et al. Am. J. hum. Genet. 46, 1112–1126 (1990).
Grosveld, F., van Assendelft, G. B., Greaves, D. R. & Kollias, G. Cell 51, 975–985 (1987).
Higgs, D. R. et al. Genes Dev. (in the press).
Hatton, C. S. R. et al. Blood 76, 221–227 (1990).
Baroin, A., Prat, A. & Caron, F. Nucleic Acids Res. 15, 1717–1728 (1987).
Forney, J. D. & Blackburn, E. H. Molec. cell. Biol. 8, 251–258 (1988).
Spangler, E. A., Ryan, T. & Blackburn, E. H. Nucleic Acids Res. 16, 5569–5585 (1988).
Levis, R. W. Cell 58, 791–801 (1989).
Biessmann, H., Carter, S. B. & Mason, J. M. Proc natn. Acad. Sci. U.S.A. 87, 1758–1761 (1990).
Biessmann, H. et al. Cell 61, 663–673 (1990).
Corcoran, L. M., Thompson, J. K., Walliker, D. & Kemp, D. J. Cell 53, 807–813 (1988).
Pologe, L. G. & Ravetch, J. V. Cell 55, 869–874 (1988).
Cappai, R. et al. Molec. cell. Biol. 9, 3584–3587 (1989).
Watson, J. D. Nature New Biol. 239, 197–201 (1972).
Murray, A. W., Claus, T. E. & Szostak, J. W. Molec. cell. Biol. 8, 4642–4650 (1988).
Jarman, A. P. & Higgs, D. R. Am. J. hum. Genet. 43, 249–256 (1988).
Nicholls, R. D., Fischel-Ghodsian, N. & Higgs, D. R. Cell 49, 369–378 (1987).
Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning 2nd edn (Cold Spring Harbor Laboratory, New York, 1989).
Church, G. M. & Gilbert, W. Proc. natn. Acad. Sci. U.S.A. 81, 1991–1995 (1984).
Sealey, P. G., Whittaker, P. A. & Southern, E. M. Nucleic Acids Res. 13, 1905–1922 (1985).
Chen, E. Y. & Seeburg, P. H. DNA 4, 165–170 (1985).
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Wilkie, A., Lamb, J., Harris, P. et al. A truncated human chromosome 16 associated with α thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n. Nature 346, 868–871 (1990). https://doi.org/10.1038/346868a0
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DOI: https://doi.org/10.1038/346868a0