Literature DB >> 28690484

Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.

Milena Simioni1, François Artiguenave2, Vincent Meyer2, Ilária C Sgardioli1, Nilma L Viguetti-Campos1, Isabella Lopes Monlleó3, Andréa T Maciel-Guerra1, Carlos E Steiner1, Vera L Gil-da-Silva-Lopes1.   

Abstract

Balanced chromosomal rearrangements (BCR) are associated with abnormal phenotypes in approximately 6% of balanced translocations and 9.4% of balanced inversions. Abnormal phenotypes can be caused by disruption of genes at the breakpoints, deletions, or positional effects. Conventional cytogenetic techniques have a limited resolution and do not enable a thorough genetic investigation. Molecular techniques applied to BCR carriers can contribute to the characterization of this type of chromosomal rearrangement and to the phenotype-genotype correlation. Fifteen individuals among 35 with abnormal phenotypes and BCR were selected for further investigation by molecular techniques. Chromosomal rearrangements involved 11 reciprocal translocations, 3 inversions, and 1 balanced insertion. Array genomic hybridization (AGH) was performed and genomic imbalances were detected in 20% of the cases, 1 at a rearrangement breakpoint and 2 further breakpoints in other chromosomes. Alterations were further confirmed by FISH and associated with the phenotype of the carriers. In the analyzed cases not showing genomic imbalances by AGH, next-generation sequencing (NGS), using whole genome libraries, prepared following the Illumina TruSeq DNA PCR-Free protocol (Illumina®) and then sequenced on an Illumina HiSEQ 2000 as 150-bp paired-end reads, was done. The NGS results suggested breakpoints in 7 cases that were similar or near those estimated by karyotyping. The genes overlapping 6 breakpoint regions were analyzed. Follow-up of BCR carriers would improve the knowledge about these chromosomal rearrangements and their consequences.

Entities:  

Keywords:  Abnormal phenotypes; Balanced chromosomal rearrangements; Microarray; Next-generation sequencing

Year:  2017        PMID: 28690484      PMCID: PMC5498958          DOI: 10.1159/000477084

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  46 in total

1.  Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing.

Authors:  Andrew L Feldman; Ahmet Dogan; David I Smith; Mark E Law; Stephen M Ansell; Sarah H Johnson; Julie C Porcher; Nazan Ozsan; Eric D Wieben; Bruce W Eckloff; George Vasmatzis
Journal:  Blood       Date:  2010-10-28       Impact factor: 22.113

2.  Satb2 regulates callosal projection neuron identity in the developing cerebral cortex.

Authors:  Elizabeth A Alcamo; Laura Chirivella; Marcel Dautzenberg; Gergana Dobreva; Isabel Fariñas; Rudolf Grosschedl; Susan K McConnell
Journal:  Neuron       Date:  2008-02-07       Impact factor: 17.173

3.  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

4.  Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.

Authors:  Julia Baptista; Catherine Mercer; Elena Prigmore; Susan M Gribble; Nigel P Carter; Viv Maloney; N Simon Thomas; Patricia A Jacobs; John A Crolla
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

5.  Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing.

Authors:  Wei Chen; Reinhard Ullmann; Claudia Langnick; Corinna Menzel; Zofia Wotschofsky; Hao Hu; Andreas Döring; Yuhui Hu; Hui Kang; Andreas Tzschach; Maria Hoeltzenbein; Heidemarie Neitzel; Susanne Markus; Eberhard Wiedersberg; Gerd Kistner; Conny M A van Ravenswaaij-Arts; Tjitske Kleefstra; Vera M Kalscheuer; Hans-Hilger Ropers
Journal:  Eur J Hum Genet       Date:  2009-12-02       Impact factor: 4.246

6.  The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.

Authors:  G Van Buggenhout; C Van Ravenswaaij-Arts; N Mc Maas; R Thoelen; A Vogels; Dominique Smeets; I Salden; G Matthijs; J-P Fryns; J R Vermeesch
Journal:  Eur J Med Genet       Date:  2005 Jul-Sep       Impact factor: 2.708

7.  Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.

Authors:  I Slade; P Stephens; J Douglas; K Barker; L Stebbings; F Abbaszadeh; K Pritchard-Jones; R Cole; B Pizer; C Stiller; G Vujanic; R H Scott; M R Stratton; N Rahman
Journal:  J Med Genet       Date:  2009-11-30       Impact factor: 6.318

8.  Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.

Authors:  Caroline Schluth-Bolard; Bruno Delobel; Damien Sanlaville; Odile Boute; Jean-Marie Cuisset; Sylvie Sukno; Audrey Labalme; Bénédicte Duban-Bedu; Ghislaine Plessis; Sylvie Jaillard; Christèle Dubourg; Catherine Henry; Josette Lucas; Sylvie Odent; Laurent Pasquier; Henri Copin; Philippe Latour; Marie-Pierre Cordier; Gwenaël Nadeau; Marianne Till; Patrick Edery; Joris Andrieux
Journal:  Eur J Med Genet       Date:  2009-06-06       Impact factor: 2.708

Review 9.  Long-range control of gene expression: emerging mechanisms and disruption in disease.

Authors:  Dirk A Kleinjan; Veronica van Heyningen
Journal:  Am J Hum Genet       Date:  2004-11-17       Impact factor: 11.025

10.  Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

Authors:  M De Gregori; R Ciccone; P Magini; T Pramparo; S Gimelli; J Messa; F Novara; A Vetro; E Rossi; P Maraschio; M C Bonaglia; C Anichini; G B Ferrero; M Silengo; E Fazzi; A Zatterale; R Fischetto; C Previderé; S Belli; A Turci; G Calabrese; F Bernardi; E Meneghelli; M Riegel; M Rocchi; S Guerneri; F Lalatta; L Zelante; C Romano; M Fichera; T Mattina; G Arrigo; M Zollino; S Giglio; F Lonardo; A Bonfante; A Ferlini; F Cifuentes; H Van Esch; L Backx; A Schinzel; J R Vermeesch; O Zuffardi
Journal:  J Med Genet       Date:  2007-08-31       Impact factor: 6.318

View more
  2 in total

1.  Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements.

Authors:  Jesper Eisfeldt; Maria Pettersson; Francesco Vezzi; Josephine Wincent; Max Käller; Joel Gruselius; Daniel Nilsson; Elisabeth Syk Lundberg; Claudia M B Carvalho; Anna Lindstrand
Journal:  PLoS Genet       Date:  2019-02-08       Impact factor: 5.917

2.  Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal Rearrangements.

Authors:  N B Satkin; B Karaman; S Ergin; H Kayserili; I H Kalelioglu; R Has; A Yuksel; S Basaran
Journal:  Balkan J Med Genet       Date:  2021-03-23       Impact factor: 0.519

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.