Literature DB >> 10924407

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

H Varley1, S Di, S W Scherer, N J Royle.   

Abstract

We have developed a strategy for the isolation of terminal deletion breakpoints from any chromosome that has been healed by de novo addition of a telomere repeat array. Breakpoints at 7q32 and 22q13.3 have been isolated and characterized in two patients (patients FB336R and AJ). Both truncated chromosomes have been healed by the addition of a novel telomere, with such an addition possibly mediated by the enzyme telomerase. The breakpoint at 7q32 in patient FB336R shows a structure similar to that of breakpoints on other chromosomes that have been healed in this way. However, the breakpoint at 22q13.3 in patient AJ has 10 nucleotides of unknown origin inserted between the sequence unique to chromosome 22q and the start of the telomere repeat array. This unusual structure is suggestive of a multistep healing event resulting in de novo telomere addition at this breakpoint, and possible mechanisms are discussed.

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Year:  2000        PMID: 10924407      PMCID: PMC1287521          DOI: 10.1086/303050

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  49 in total

1.  High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution.

Authors:  D M Baird; J Coleman; Z H Rosser; N J Royle
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  The Stability of Broken Ends of Chromosomes in Zea Mays.

Authors:  B McClintock
Journal:  Genetics       Date:  1941-03       Impact factor: 4.562

3.  Recognition of a chromosome truncation site associated with alpha-thalassaemia by human telomerase.

Authors:  G B Morin
Journal:  Nature       Date:  1991-10-03       Impact factor: 49.962

4.  Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q.

Authors:  A Tunnacliffe; C Jones; D Le Paslier; R Todd; D Cherif; M Birdsall; L Devenish; C Yousry; F E Cotter; M R James
Journal:  Genome Res       Date:  1999-01       Impact factor: 9.043

5.  Telomerase activity in human germline and embryonic tissues and cells.

Authors:  W E Wright; M A Piatyszek; W E Rainey; W Byrd; J W Shay
Journal:  Dev Genet       Date:  1996

6.  Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domains.

Authors:  J Flint; G P Bates; K Clark; A Dorman; D Willingham; B A Roe; G Micklem; D R Higgs; E J Louis
Journal:  Hum Mol Genet       Date:  1997-08       Impact factor: 6.150

7.  Cloning of human telomeres by complementation in yeast.

Authors:  S H Cross; R C Allshire; S J McKay; N I McGill; H J Cooke
Journal:  Nature       Date:  1989-04-27       Impact factor: 49.962

8.  Tetrahymena telomerase catalyzes nucleolytic cleavage and nonprocessive elongation.

Authors:  K Collins; C W Greider
Journal:  Genes Dev       Date:  1993-07       Impact factor: 11.361

9.  Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

Authors:  A Schinzel; P Auf der Maur; H Moser
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

10.  Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere.

Authors:  D M Baird; A J Jeffreys; N J Royle
Journal:  EMBO J       Date:  1995-11-01       Impact factor: 11.598

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  22 in total

1.  Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.

Authors:  Blake C Ballif; Keiko Wakui; Marzena Gajecka; Lisa G Shaffer
Journal:  Hum Genet       Date:  2003-10-25       Impact factor: 4.132

2.  Multiple pathways suppress telomere addition to DNA breaks in the Drosophila germline.

Authors:  Michelle Beaucher; Xiao-Feng Zheng; Flavia Amariei; Yikang S Rong
Journal:  Genetics       Date:  2012-03-23       Impact factor: 4.562

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.  Telomerase-dependent and -independent chromosome healing in mouse embryonic stem cells.

Authors:  Qing Gao; Gloria E Reynolds; Andrew Wilcox; Douglas Miller; Peggie Cheung; Steven E Artandi; John P Murnane
Journal:  DNA Repair (Amst)       Date:  2008-05-23

5.  DNA amplification by breakage/fusion/bridge cycles initiated by spontaneous telomere loss in a human cancer cell line.

Authors:  Anthony W I Lo; Laure Sabatier; Bijan Fouladi; Géraldine Pottier; Michelle Ricoul; John P Murnane
Journal:  Neoplasia       Date:  2002 Nov-Dec       Impact factor: 5.715

Review 6.  Regulation of telomere addition at DNA double-strand breaks.

Authors:  Cyril Ribeyre; David Shore
Journal:  Chromosoma       Date:  2013-03-17       Impact factor: 4.316

7.  PIF1 disruption or NBS1 hypomorphism does not affect chromosome healing or fusion resulting from double-strand breaks near telomeres in murine embryonic stem cells.

Authors:  Gloria E Reynolds; Qing Gao; Douglas Miller; Bryan E Snow; Lea A Harrington; John P Murnane
Journal:  DNA Repair (Amst)       Date:  2011-09-25

Review 8.  Telomere loss as a mechanism for chromosome instability in human cancer.

Authors:  John P Murnane
Journal:  Cancer Res       Date:  2010-05-18       Impact factor: 12.701

Review 9.  Telomere dysfunction and chromosome instability.

Authors:  John P Murnane
Journal:  Mutat Res       Date:  2011-05-07       Impact factor: 2.433

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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