Literature DB >> 10869233

An optimized set of human telomere clones for studying telomere integrity and architecture.

S J Knight1, C M Lese, K S Precht, J Kuc, Y Ning, S Lucas, R Regan, M Brenan, A Nicod, N M Lawrie, D L Cardy, H Nguyen, T J Hudson, H C Riethman, D H Ledbetter, J Flint.   

Abstract

Telomere-specific clones are a valuable resource for the characterization of chromosomal rearrangements. We previously reported a first-generation set of human telomere probes consisting of 34 genomic clones, which were a known distance from the end of the chromosome ( approximately 300 kb), and 7 clones corresponding to the most distal markers on the integrated genetic/physical map (1p, 5p, 6p, 9p, 12p, 15q, and 20q). Subsequently, this resource has been optimized and completed: the size of the genomic clones has been expanded to a target size of 100-200 kb, which is optimal for use in genome-scanning methodologies, and additional probes for the remaining seven telomeres have been identified. For each clone we give an associated mapped sequence-tagged site and provide distances from the telomere estimated using a combination of fiberFISH, interphase FISH, sequence analysis, and radiation-hybrid mapping. This updated set of telomeric clones is an invaluable resource for clinical diagnosis and represents an important contribution to genetic and physical mapping efforts aimed at telomeric regions.

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Year:  2000        PMID: 10869233      PMCID: PMC1287181          DOI: 10.1086/302998

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.043


  40 in total

1.  An integrated physical map for the short arm of human chromosome 5.

Authors:  E T Peterson; R Sutherland; D L Robinson; L Chasteen; M Gersh; J Overhauser; L L Deaven; R K Moyzis; D L Grady
Journal:  Genome Res       Date:  1999-12       Impact factor: 9.043

2.  Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).

Authors:  E Holinski-Feder; E Reyniers; S Uhrig; A Golla; J Wauters; P Kroisel; P Bossuyt; I Rost; K Jedele; H Zierler; S Schwab; D Wildenauer; M R Speicher; P J Willems; T Meitinger; R F Kooy
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

3.  Recent human-specific spreading of a subtelomeric domain.

Authors:  S Monfouilloux; H Avet-Loiseau; V Amarger; I Balazs; C Pourcel; G Vergnaud
Journal:  Genomics       Date:  1998-07-15       Impact factor: 5.736

4.  A 1.2-megabase BAC/PAC contig spanning the 14q13 breakpoint of t(2; 14) in a mirror-image polydactyly patient.

Authors:  N Matsumoto; E Soeda; H Ohashi; M Fujimoto; R Kato; T Tsujita; H Tomita; S Kondo; Y Fukushima; N Niikawa
Journal:  Genomics       Date:  1997-10-01       Impact factor: 5.736

5.  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

6.  Characterization of short tandem repeats from thirty-one human telomeres.

Authors:  M Rosenberg; L Hui; J Ma; H C Nusbaum; K Clark; L Robinson; L Dziadzio; P M Swain; T Keith; T J Hudson; L G Biesecker; J Flint
Journal:  Genome Res       Date:  1997-09       Impact factor: 9.043

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.  Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.

Authors:  S J Knight; S W Horsley; R Regan; N M Lawrie; E J Maher; D L Cardy; J Flint; L Kearney
Journal:  Eur J Hum Genet       Date:  1997 Jan-Feb       Impact factor: 4.246

9.  Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes.

Authors:  B J Trask; C Friedman; A Martin-Gallardo; L Rowen; C Akinbami; J Blankenship; C Collins; D Giorgi; S Iadonato; F Johnson; W L Kuo; H Massa; T Morrish; S Naylor; O T Nguyen; S Rouquier; T Smith; D J Wong; J Youngblom; G van den Engh
Journal:  Hum Mol Genet       Date:  1998-01       Impact factor: 6.150

10.  Subtle chromosomal rearrangements in children with unexplained mental retardation.

Authors:  S J Knight; R Regan; A Nicod; S W Horsley; L Kearney; T Homfray; R M Winter; P Bolton; J Flint
Journal:  Lancet       Date:  1999-11-13       Impact factor: 79.321

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  45 in total

1.  The evolutionary origin of human subtelomeric homologies--or where the ends begin.

Authors:  Christa Lese Martin; Andrew Wong; Alyssa Gross; June Chung; Judy A Fantes; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2002-03-01       Impact factor: 11.025

2.  Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.

Authors:  Heidi A Heilstedt; Blake C Ballif; Leslie A Howard; Richard A Lewis; Samuel Stal; Catherine D Kashork; Carlos A Bacino; Stuart K Shapira; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2003-04-08       Impact factor: 11.025

Review 3.  Parental origin and timing of de novo Robertsonian translocation formation.

Authors:  Ruma Bandyopadhyay; Anita Heller; Cami Knox-DuBois; Christopher McCaskill; Sue Ann Berend; Scott L Page; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-11-06       Impact factor: 11.025

Review 4.  Telomeres: a diagnosis at the end of the chromosomes.

Authors:  B B A De Vries; R Winter; A Schinzel; C van Ravenswaaij-Arts
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

5.  Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy.

Authors:  Fan Yang; Chunbo Shao; Vettaikorumakankav Vedanarayanan; Melanie Ehrlich
Journal:  Chromosoma       Date:  2004-05-11       Impact factor: 4.316

6.  A set of BAC clones spanning the human genome.

Authors:  Martin Krzywinski; Ian Bosdet; Duane Smailus; Readman Chiu; Carrie Mathewson; Natasja Wye; Sarah Barber; Mabel Brown-John; Susanna Chan; Steve Chand; Alison Cloutier; Noreen Girn; Darlene Lee; Amara Masson; Michael Mayo; Teika Olson; Pawan Pandoh; Anna-Liisa Prabhu; Eric Schoenmakers; Miranda Tsai; Donna Albertson; Wan Lam; Chik-On Choy; Kazutoyo Osoegawa; Shaying Zhao; Pieter J de Jong; Jacqueline Schein; Steven Jones; Marco A Marra
Journal:  Nucleic Acids Res       Date:  2004-07-09       Impact factor: 16.971

7.  Molecular karyotyping using an SNP array for genomewide genotyping.

Authors:  A Rauch; F Rüschendorf; J Huang; U Trautmann; C Becker; C Thiel; K W Jones; A Reis; P Nürnberg
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

8.  Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Authors:  J B Ravnan; J H Tepperberg; P Papenhausen; A N Lamb; J Hedrick; D Eash; D H Ledbetter; C L Martin
Journal:  J Med Genet       Date:  2005-09-30       Impact factor: 6.318

9.  Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.

Authors:  C D M van Karnebeek; C Koevoets; S Sluijter; E K Bijlsma; D F M C Smeets; E J Redeker; R C M Hennekam; J M N Hoovers
Journal:  J Med Genet       Date:  2002-08       Impact factor: 6.318

10.  A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome.

Authors:  Naoki Harada; Remco Visser; Angie Dawson; Makoto Fukamachi; Mie Iwakoshi; Nobuhiko Okamoto; Tatsuya Kishino; Norio Niikawa; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2004-07-16       Impact factor: 3.172

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