Literature DB >> 18319076

Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.

Anne W Higgins1, Fowzan S Alkuraya, Amy F Bosco, Kerry K Brown, Gail A P Bruns, Diana J Donovan, Robert Eisenman, Yanli Fan, Chantal G Farra, Heather L Ferguson, James F Gusella, David J Harris, Steven R Herrick, Chantal Kelly, Hyung-Goo Kim, Shotaro Kishikawa, Bruce R Korf, Shashikant Kulkarni, Eric Lally, Natalia T Leach, Emma Lemyre, Janine Lewis, Azra H Ligon, Weining Lu, Richard L Maas, Marcy E MacDonald, Steven D P Moore, Roxanna E Peters, Bradley J Quade, Fabiola Quintero-Rivera, Irfan Saadi, Yiping Shen, Jay Shendure, Robin E Williamson, Cynthia C Morton.   

Abstract

Apparently balanced chromosomal rearrangements in individuals with major congenital anomalies represent natural experiments of gene disruption and dysregulation. These individuals can be studied to identify novel genes critical in human development and to annotate further the function of known genes. Identification and characterization of these genes is the goal of the Developmental Genome Anatomy Project (DGAP). DGAP is a multidisciplinary effort that leverages the recent advances resulting from the Human Genome Project to increase our understanding of birth defects and the process of human development. Clinically significant phenotypes of individuals enrolled in DGAP are varied and, in most cases, involve multiple organ systems. Study of these individuals' chromosomal rearrangements has resulted in the mapping of 77 breakpoints from 40 chromosomal rearrangements by FISH with BACs and fosmids, array CGH, Southern-blot hybridization, MLPA, RT-PCR, and suppression PCR. Eighteen chromosomal breakpoints have been cloned and sequenced. Unsuspected genomic imbalances and cryptic rearrangements were detected, but less frequently than has been reported previously. Chromosomal rearrangements, both balanced and unbalanced, in individuals with multiple congenital anomalies continue to be a valuable resource for gene discovery and annotation.

Entities:  

Mesh:

Year:  2008        PMID: 18319076      PMCID: PMC2427206          DOI: 10.1016/j.ajhg.2008.01.011

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


  36 in total

1.  De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

Review 2.  DNA breakage and repair.

Authors:  P A Jeggo
Journal:  Adv Genet       Date:  1998       Impact factor: 1.944

3.  An improved PCR method for walking in uncloned genomic DNA.

Authors:  P D Siebert; A Chenchik; D E Kellogg; K A Lukyanov; S A Lukyanov
Journal:  Nucleic Acids Res       Date:  1995-03-25       Impact factor: 16.971

4.  Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

Authors:  P N Ray; B Belfall; C Duff; C Logan; V Kean; M W Thompson; J E Sylvester; J L Gorski; R D Schmickel; R G Worton
Journal:  Nature       Date:  1985 Dec 19-1986 Jan 1       Impact factor: 49.962

5.  Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

Authors:  D Viskochil; A M Buchberg; G Xu; R M Cawthon; J Stevens; R K Wolff; M Culver; J C Carey; N G Copeland; N A Jenkins
Journal:  Cell       Date:  1990-07-13       Impact factor: 41.582

6.  Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination.

Authors:  R G Sargent; M A Brenneman; J H Wilson
Journal:  Mol Cell Biol       Date:  1997-01       Impact factor: 4.272

7.  Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).

Authors:  S Ishikiriyama; H Tonoki; Y Shibuya; S Chin; N Harada; K Abe; N Niikawa
Journal:  Am J Med Genet       Date:  1989-08

8.  Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.

Authors:  N B Spinner; E B Rand; P Fortina; A Genin; R Taub; A Semeraro; D A Piccoli
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

Review 9.  Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3).

Authors:  N Tommerup; C B van der Hagen; A Heiberg
Journal:  Am J Med Genet       Date:  1992-09-15

Review 10.  Position effect in human genetic disease.

Authors:  D J Kleinjan; V van Heyningen
Journal:  Hum Mol Genet       Date:  1998       Impact factor: 6.150

View more
  52 in total

1.  Large clinically consequential imbalances detected at the breakpoints of apparently balanced and inherited chromosome rearrangements.

Authors:  Sarah T South; Lyndsey Rector; Emily Aston; Leslie Rowe; Samuel P Yang
Journal:  J Mol Diagn       Date:  2010-07-01       Impact factor: 5.568

2.  Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.

Authors:  Zhishuo Ou; Paweł Stankiewicz; Zhilian Xia; Amy M Breman; Brian Dawson; Joanna Wiszniewska; Przemyslaw Szafranski; M Lance Cooper; Mitchell Rao; Lina Shao; Sarah T South; Karlene Coleman; Paul M Fernhoff; Marcel J Deray; Sally Rosengren; Elizabeth R Roeder; Victoria B Enciso; A Craig Chinault; Ankita Patel; Sung-Hae L Kang; Chad A Shaw; James R Lupski; Sau W Cheung
Journal:  Genome Res       Date:  2011-01       Impact factor: 9.043

3.  Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

Authors:  Hyung-Goo Kim; Hyun-Taek Kim; Natalia T Leach; Fei Lan; Reinhard Ullmann; Asli Silahtaroglu; Ingo Kurth; Anja Nowka; Ihn Sik Seong; Yiping Shen; Michael E Talkowski; Douglas Ruderfer; Ji-Hyun Lee; Caron Glotzbach; Kyungsoo Ha; Susanne Kjaergaard; Alex V Levin; Bernd F Romeike; Tjitske Kleefstra; Oliver Bartsch; Sarah H Elsea; Ethylin Wang Jabs; Marcy E MacDonald; David J Harris; Bradley J Quade; Hans-Hilger Ropers; Lisa G Shaffer; Kerstin Kutsche; Lawrence C Layman; Niels Tommerup; Vera M Kalscheuer; Yang Shi; Cynthia C Morton; Cheol-Hee Kim; James F Gusella
Journal:  Am J Hum Genet       Date:  2012-07-05       Impact factor: 11.025

Review 4.  Balanced translocations in mental retardation.

Authors:  Geert Vandeweyer; R Frank Kooy
Journal:  Hum Genet       Date:  2009-04-05       Impact factor: 4.132

5.  SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome.

Authors:  S Bens; T Zichner; A M Stütz; A Caliebe; R Wagener; K Hoff; J O Korbel; P von Bismarck; R Siebert
Journal:  Genes Immun       Date:  2014-01-23       Impact factor: 2.676

6.  Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

Authors:  Michael E Talkowski; Carl Ernst; Adrian Heilbut; Colby Chiang; Carrie Hanscom; Amelia Lindgren; Andrew Kirby; Shangtao Liu; Bhavana Muddukrishna; Toshiro K Ohsumi; Yiping Shen; Mark Borowsky; Mark J Daly; Cynthia C Morton; James F Gusella
Journal:  Am J Hum Genet       Date:  2011-04-08       Impact factor: 11.025

7.  Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis.

Authors:  Ilse Feenstra; Nicolien Hanemaaijer; Birgit Sikkema-Raddatz; Helger Yntema; Trijnie Dijkhuizen; Dorien Lugtenberg; Joke Verheij; Andrew Green; Roel Hordijk; William Reardon; Bert de Vries; Han Brunner; Ernie Bongers; Nicole de Leeuw; Conny van Ravenswaaij-Arts
Journal:  Eur J Hum Genet       Date:  2011-06-29       Impact factor: 4.246

8.  Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.

Authors:  Cinthya J Zepeda-Mendoza; Jonas Ibn-Salem; Tammy Kammin; David J Harris; Debra Rita; Karen W Gripp; Jennifer J MacKenzie; Andrea Gropman; Brett Graham; Ranad Shaheen; Fowzan S Alkuraya; Campbell K Brasington; Edward J Spence; Diane Masser-Frye; Lynne M Bird; Erica Spiegel; Rebecca L Sparkes; Zehra Ordulu; Michael E Talkowski; Miguel A Andrade-Navarro; Peter N Robinson; Cynthia C Morton
Journal:  Am J Hum Genet       Date:  2017-07-20       Impact factor: 11.025

9.  Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Authors:  B Vona; C Neuner; N El Hajj; E Schneider; R Farcas; V Beyer; U Zechner; A Keilmann; M Poot; O Bartsch; I Nanda; T Haaf
Journal:  Mol Syndromol       Date:  2013-10-04

10.  Towards a comprehensive structural variation map of an individual human genome.

Authors:  Andy W Pang; Jeffrey R MacDonald; Dalila Pinto; John Wei; Muhammad A Rafiq; Donald F Conrad; Hansoo Park; Matthew E Hurles; Charles Lee; J Craig Venter; Ewen F Kirkness; Samuel Levy; Lars Feuk; Stephen W Scherer
Journal:  Genome Biol       Date:  2010-05-19       Impact factor: 13.583

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.