Literature DB >> 11151680

Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation.

A E Wandstrat1, S Schwartz.   

Abstract

An inverted duplication of chromosome 15 [inv dup(15)] is the most common supernumerary marker chromosome, comprising approximately 50% of all chromosomes in this class. Structurally, the inv dup(15) is a mirror image with the central axis defining a distal break within either the heterochromatic alpha-satellite array or along the euchromatin in the long (q) arm of the chromosome. There are several types of inv dup(15), classified by the amount of euchromatic material present. Generally, they are bisatellited, pseudodicentric and have a breakpoint in 15q11-q14. A suggested mechanism of formation of inv dup(15) involves illegitimate recombination between homologous chromosomes followed by nondisjunction and centromere inactivation. The proximal portion of chromosome 15 contains several low-copy repeat sequence families and it has been hypothesized that errors in pairing among these repeats may result in structural rearrangements of this chromosome including the inv dup(15). To test this hypothesis and to determine the mechanism of formation, the inv dup(15) from four cases was isolated in somatic cell hybrids and polymerase chain reaction microsatellite markers were used to determine the origin of exchange. Two appeared to result from interchromosomal and two from intrachromosomal exchange, one of which occurred post-recombination. In addition, a detailed physical map of the breakpoint region in the largest inv dup(15) was constructed placing eight new sequence-tagged sites and ten new bacterial artificial chromosome markers in the region.

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Year:  2000        PMID: 11151680     DOI: 10.1007/s004120000103

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  14 in total

1.  High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.

Authors:  Nicholas J Wang; Dahai Liu; Alexander S Parokonny; N Carolyn Schanen
Journal:  Am J Hum Genet       Date:  2004-06-11       Impact factor: 11.025

2.  Infertility and marker chromosomes: application of molecular cytogenetic techniques in a case of inv dup(15).

Authors:  Tania M Vulcani-Freitas; Vera L Gil-da-Silva-Lopes; Marileila Varella-Garcia; Andréa T Maciel-Guerra
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

3.  Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Authors:  Dorota A Kwasnicka-Crawford; Wendy Roberts; Stephen W Scherer
Journal:  J Autism Dev Disord       Date:  2007-04

Review 4.  From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.

Authors:  Beverly S Emanuel; Sulagna C Saitta
Journal:  Nat Rev Genet       Date:  2007-11       Impact factor: 53.242

5.  Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster.

Authors:  Devin P Locke; Nicoletta Archidiacono; Doriana Misceo; Maria Francesca Cardone; Stephane Deschamps; Bruce Roe; Mariano Rocchi; Evan E Eichler
Journal:  Genome Biol       Date:  2003-07-15       Impact factor: 13.583

6.  Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Authors:  S E Roberts; F Maggouta; N S Thomas; P A Jacobs; J A Crolla
Journal:  Am J Hum Genet       Date:  2003-10-14       Impact factor: 11.025

7.  A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma.

Authors:  C Córdova-Fletes; M G Domínguez; A Vázquez-Cárdenas; L E Figuera; V A Neira; A Rojas-Martínez; R Ortiz-López
Journal:  Mol Syndromol       Date:  2012-08-01

8.  15q Duplication Syndrome: Report on the First Patient from Ecuador with an Unusual Clinical Presentation.

Authors:  Esteban Ortiz-Prado; Ana Lucía Iturralde; Katherine Simbaña-Rivera; Lenin Gómez-Barreno; Iván Hidalgo; Mario Rubio-Neira; Nicolás Espinosa; Juan Izquierdo-Condoy; María Emilia Arteaga-Espinosa; Alex Lister; Andrés López-Cortés; Alejandro Cabrera-Andrade
Journal:  Case Rep Med       Date:  2021-05-03

9.  De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s.

Authors:  Elena Rossi; Roberto Giorda; Maria Clara Bonaglia; Stefania Di Candia; Elena Grechi; Adriana Franzese; Fiorenza Soli; Francesca Rivieri; Maria Grazia Patricelli; Donatella Saccilotto; Aldo Bonfante; Sabrina Giglio; Silvana Beri; Mariano Rocchi; Orsetta Zuffardi
Journal:  PLoS One       Date:  2012-06-14       Impact factor: 3.240

10.  Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorder.

Authors:  Karim Ouldim; Abdelhafid Natiq; Philippe Jonveaux; Abdelaziz Sefiani
Journal:  J Biomed Biotechnol       Date:  2007-03-20
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