Literature DB >> 17264869

Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.

Cécile Mignon-Ravix1, Danielle Depetris, Judith J Luciani, Cristina Cuoco, Malgorzata Krajewska-Walasek, Chantal Missirian, Patrick Collignon, Bruno Delobel, Marie-Françoise Croquette, Anne Moncla, Peter M Kroisel, Marie-Geneviève Mattei.   

Abstract

Unbalanced translocations, that involve the proximal chromosome 15 long arm and the telomeric region of a partner chromosome, result in a karyotype of 45 chromosomes with monosomy of the proximal 15q imprinted region. Here, we present our analysis of eight such unbalanced translocations that, depending on the parental origin of the rearranged chromosome, were associated with either Prader-Willi or Angelman syndrome. First, using FISH with specific BAC clones, we characterized the chromosome 15 breakpoint of each translocation and demonstrate that four of them are clustered in a small 460 kb interval located in the proximal 15q14 band. Second, analyzing the sequence of this region, we demonstrate the proximity of a low-copy repeat 15 (LCR15)-duplicon element that is known to facilitate recombination events at meiosis and to promote rearrangements. The presence, in this region, of both a cluster of translocation breakpoints and a LCR15-duplicon element defines a new breakpoint cluster (BP6), which, to our knowledge, is the most distal breakpoint cluster described in proximal 15q. Third, we demonstrate that the breakpoints for other rearrangements including large inv dup (15) chromosomes do not map to BP6, suggesting that it is specific to translocations. Finally, the translocation breakpoints located within BP6 result in very large proximal 15q deletions providing new informative genotype-phenotype correlations.

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Year:  2007        PMID: 17264869     DOI: 10.1038/sj.ejhg.5201775

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  13 in total

1.  Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.

Authors:  B W M van Bon; H C Mefford; B Menten; D A Koolen; A J Sharp; W M Nillesen; J W Innis; T J L de Ravel; C L Mercer; M Fichera; H Stewart; L E Connell; K Ounap; K Lachlan; B Castle; N Van der Aa; C van Ravenswaaij; M A Nobrega; C Serra-Juhé; I Simonic; N de Leeuw; R Pfundt; E M Bongers; C Baker; P Finnemore; S Huang; V K Maloney; J A Crolla; M van Kalmthout; M Elia; G Vandeweyer; J P Fryns; S Janssens; N Foulds; S Reitano; K Smith; S Parkel; B Loeys; C G Woods; A Oostra; F Speleman; A C Pereira; A Kurg; L Willatt; S J L Knight; J R Vermeesch; C Romano; J C Barber; G Mortier; L A Pérez-Jurado; F Kooy; H G Brunner; E E Eichler; T Kleefstra; B B A de Vries
Journal:  J Med Genet       Date:  2009-04-15       Impact factor: 6.318

2.  Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.

Authors:  Soo-Jeong Kim; Jennifer L Miller; Paul J Kuipers; Jennifer Ruth German; Arthur L Beaudet; Trilochan Sahoo; Daniel J Driscoll
Journal:  Eur J Hum Genet       Date:  2011-11-02       Impact factor: 4.246

3.  Copy number variants: a new molecular frontier in clinical psychiatry.

Authors:  Daniel Moreno-De-Luca; Joseph F Cubells
Journal:  Curr Psychiatry Rep       Date:  2011-04       Impact factor: 5.285

4.  Partners in crime: Tbf1 and Vid22 promote expansions of long human telomeric repeats at an interstitial chromosome position in yeast.

Authors:  Elina A Radchenko; Anna Y Aksenova; Kirill V Volkov; Alexander A Shishkin; Youri I Pavlov; Sergei M Mirkin
Journal:  PNAS Nexus       Date:  2022-06-08

5.  An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.

Authors:  Merlin G Butler; Douglas C Bittel; Nataliya Kibiryeva; Linda D Cooley; Shihui Yu
Journal:  Am J Med Genet A       Date:  2010-02       Impact factor: 2.802

6.  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

7.  Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation.

Authors:  Frenny Sheth; Thomas Liehr; Krati Shah; Jayesh Sheth
Journal:  Mol Cytogenet       Date:  2015-07-22       Impact factor: 2.009

8.  Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.

Authors:  Anita S Y Kan; Elizabeth T Lau; W F Tang; Sario S Y Chan; Simon C K Ding; Kelvin Y K Chan; C P Lee; Pui Wah Hui; Brian H Y Chung; K Y Leung; Teresa Ma; Wing C Leung; Mary H Y Tang
Journal:  PLoS One       Date:  2014-02-05       Impact factor: 3.240

9.  A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment.

Authors:  Jing Yang; Yongchen Yang; Yi Huang; Yan Hu; Xi Chen; Hengjuan Sun; Zhibao Lv; Qian Cheng; Liming Bao
Journal:  BMC Med Genet       Date:  2013-01-15       Impact factor: 2.103

10.  Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Authors:  Kerry A Pettigrew; Emily Reeves; Ruth Leavett; Marianna E Hayiou-Thomas; Anahita Sharma; Nuala H Simpson; Angela Martinelli; Paul Thompson; Charles Hulme; Margaret J Snowling; Dianne F Newbury; Silvia Paracchini
Journal:  PLoS One       Date:  2015-08-11       Impact factor: 3.240

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