Literature DB >> 8842736

Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elements.

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.

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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


  13 in total

1.  Molecular-cytogenetic detection of a deletion of 1p36.3.

Authors:  F Giraudeau; D Aubert; I Young; S Horsley; S Knight; L Kearney; G Vergnaud; J Flint
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Refinement of the genetic cause of ATR-16.

Authors:  Cornelis L Harteveld; Marjolein Kriek; Emilia K Bijlsma; Zoran Erjavec; Deepak Balak; Marion Phylipsen; Astrid Voskamp; Emmanora di Capua; Stefan J White; Piero C Giordano
Journal:  Hum Genet       Date:  2007-06-28       Impact factor: 4.132

3.  Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.

Authors:  Svetlana A Yatsenko; Ellen K Brundage; Erin K Roney; Sau Wai Cheung; A Craig Chinault; James R Lupski
Journal:  Hum Mol Genet       Date:  2009-03-17       Impact factor: 6.150

4.  The molecular basis of α-thalassemia.

Authors:  Douglas R Higgs
Journal:  Cold Spring Harb Perspect Med       Date:  2013-01-01       Impact factor: 6.915

Review 5.  Telomeres and genomic evolution.

Authors:  Duncan M Baird
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-03-05       Impact factor: 6.237

6.  Subtelomeric rearrangements in idiopathic mental retardation.

Authors:  Gopalrao V N Velagaleti; Sally S Robinson; Bobby M Rouse; Vijay S Tonk; Lillian H Lockhart
Journal:  Indian J Pediatr       Date:  2005-08       Impact factor: 1.967

7.  Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilization.

Authors:  Svetlana A Yatsenko; Patricia Hixson; Erin K Roney; Daryl A Scott; Christian P Schaaf; Yu-tze Ng; Robbin Palmer; Richard B Fisher; Ankita Patel; Sau Wai Cheung; James R Lupski
Journal:  Hum Genet       Date:  2012-08-14       Impact factor: 4.132

Review 8.  Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis.

Authors:  S J Knight; J Flint
Journal:  J Med Genet       Date:  2000-06       Impact factor: 6.318

9.  Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.

Authors:  H Varley; S Di; S W Scherer; N J Royle
Journal:  Am J Hum Genet       Date:  2000-08-01       Impact factor: 11.025

10.  Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

Authors:  Carla S D'Angelo; Marzena Gajecka; Chong A Kim; Andrew J Gentles; Caron D Glotzbach; Lisa G Shaffer; Célia P Koiffmann
Journal:  Hum Genet       Date:  2009-03-07       Impact factor: 4.132

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