Literature DB >> 16133173

Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?

Manuela De Gregori1, Tiziano Pramparo, Luigi Memo, Giorgio Gimelli, Jole Messa, Mariano Rocchi, Maria Grazia Patricelli, Roberto Ciccone, Roberto Giorda, Orsetta Zuffardi.   

Abstract

We describe the characterization of an interstitial duplication of 12p, dup(12)(p11.21p13.31), by array-CGH and FISH in a patient with mental retardation and dysmorphic features. The sequence analysis of the breakpoints revealed the presence of homologous low copy repeats (LCRs) flanking the duplication region, thus suggesting that they have mediated the rearrangement. Pip-maker analysis showed that a third cluster of homologous LCRs lie distally to the two mediating the 12p duplication. We hypothesize that this duplication might be a new recurrent rearrangement and that, thanks to the different orientations of the homologous regions lying within each cluster, the three clusters are responsible for at least some of the several 12p aneuploidies reported in the literature such as direct and inverted duplications, deletions and supernumerary analphoid chromosomes. Moreover, we excluded that polymorphic inversions between these three clusters are present in the normal population.

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Year:  2005        PMID: 16133173     DOI: 10.1007/s00439-005-0008-x

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  30 in total

1.  De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism.

Authors:  J Oldenburg; S Rost; O El-Maarri; M Leuer; K Olek; C R Müller; R Schwaab
Journal:  Blood       Date:  2000-10-15       Impact factor: 22.113

2.  A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

Authors:  L R Osborne; M Li; B Pober; D Chitayat; J Bodurtha; A Mandel; T Costa; T Grebe; S Cox; L C Tsui; S W Scherer
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

3.  Williams-Beuren syndrome: a model of recurrent genomic mutation.

Authors:  Alberto Luis Pérez Jurado
Journal:  Horm Res       Date:  2003

4.  Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions.

Authors:  Marco Venturin; Cristina Gervasini; Francesca Orzan; Angela Bentivegna; Lucia Corrado; Patrizia Colapietro; Alessandra Friso; Romano Tenconi; Meena Upadhyaya; Lidia Larizza; Paola Riva
Journal:  Hum Genet       Date:  2004-04-21       Impact factor: 4.132

5.  Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.

Authors:  P A Jacobs; C Browne; N Gregson; C Joyce; H White
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

Review 6.  Segmental duplications and the evolution of the primate genome.

Authors:  Rhea Vallente Samonte; Evan E Eichler
Journal:  Nat Rev Genet       Date:  2002-01       Impact factor: 53.242

Review 7.  Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".

Authors:  A Rauch; U Trautmann; R A Pfeiffer
Journal:  Am J Med Genet       Date:  1996-05-03

8.  The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats.

Authors:  Aikaterini Barbouti; Pawel Stankiewicz; Chad Nusbaum; Christina Cuomo; April Cook; Mattias Höglund; Bertil Johansson; Anne Hagemeijer; Sung-Sup Park; Felix Mitelman; James R Lupski; Thoas Fioretos
Journal:  Am J Hum Genet       Date:  2003-12-08       Impact factor: 11.025

9.  Localization of chi1-related helicase genes to human chromosome regions 12p11 and 12p13: similarity between parts of these genes and conserved human telomeric-associated DNA.

Authors:  J Amann; M Valentine; V J Kidd; J M Lahti
Journal:  Genomics       Date:  1996-03-01       Impact factor: 5.736

10.  Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Authors:  Lisenka E L M Vissers; Bert B A de Vries; Kazutoyo Osoegawa; Irene M Janssen; Ton Feuth; Chik On Choy; Huub Straatman; Walter van der Vliet; Erik H L P G Huys; Anke van Rijk; Dominique Smeets; Conny M A van Ravenswaaij-Arts; Nine V Knoers; Ineke van der Burgt; Pieter J de Jong; Han G Brunner; Ad Geurts van Kessel; Eric F P M Schoenmakers; Joris A Veltman
Journal:  Am J Hum Genet       Date:  2003-11-18       Impact factor: 11.025

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  2 in total

1.  High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications.

Authors:  Johan H Gibcus; Klaas Kok; Lorian Menkema; Mario A Hermsen; Mirjam Mastik; Philip M Kluin; Jacqueline E van der Wal; Ed Schuuring
Journal:  Hum Genet       Date:  2006-12-15       Impact factor: 4.132

2.  Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay.

Authors:  Jakeline Santos Oliveira; Tatiana Mozer Joaquim; Rosana Aparecida Bicudo da Silva; Deise Helena de Souza; Lúcia Regina Martelli; Danilo Moretti-Ferreira
Journal:  Genet Mol Biol       Date:  2020-02-10       Impact factor: 1.771

  2 in total

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