| Literature DB >> 8842736 |
J Flint1, J Rochette, C F Craddock, C Dodé, B Vignes, S W Horsley, L Kearney, V J Buckle, H Ayyub, D R Higgs.
Abstract
We have characterised a subtelomeric rearrangement involving the short arm of chromosome 16 that gives rise to alpha-thalassaemia by deleting the major, remote regulatory element controlling alpha-globin expression. The chromosomal breakpoint lies in an Alu family repeat located only approximately 105 kb from the 16p subtelomeric region. The broken chromosome has been stabilised with a newly positioned telomere acquired by recombination between this 16p Alu element and a closely related subtelomeric Alu element of the Sx subfamily. It seems most likely that this abnormal chromosome has been rescued by the mechanism of telomere capture which may reflect a more general process by which subtelomeric sequences are normally dispersed between chromosomal ends.Entities:
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Year: 1996 PMID: 8842736 DOI: 10.1093/hmg/5.8.1163
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150