Literature DB >> 29223973

Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.

Solveig Heide1, Sandra Chantot-Bastaraud1, Boris Keren2, Madeleine D Harbison3, Salah Azzi4, Sylvie Rossignol5,6, Caroline Michot7, Marilyn Lackmy-Port Lys8, Bénédicte Demeer9, Claudine Heinrichs10, Ron S Newfield11,12, Pierre Sarda13, Lionel Van Maldergem14, Véronique Trifard15, Eloise Giabicani16,17,18, Jean-Pierre Siffroi1, Yves Le Bouc16,17,18, Irène Netchine16,17,18, Frédéric Brioude16,17,18.   

Abstract

BACKGROUND: The 11p15 region contains two clusters of imprinted genes. Opposite genetic and epigenetic anomalies of this region result in two distinct growth disturbance syndromes: Beckwith-Wiedemann (BWS) and Silver-Russell syndromes (SRS). Cytogenetic rearrangements within this region represent less than 3% of SRS and BWS cases. Among these, 11p15 duplications were infrequently reported and interpretation of their pathogenic effects is complex.
OBJECTIVES: To report cytogenetic and methylation analyses in a cohort of patients with SRS/BWS carrying 11p15 duplications and establish genotype/phenotype correlations.
METHODS: From a cohort of patients with SRS/BWS with an abnormal methylation profile (using ASMM-RTQ-PCR), we used SNP-arrays to identify and map the 11p15 duplications. We report 19 new patients with SRS (n=9) and BWS (n=10) carrying de novo or familial 11p15 duplications, which completely or partially span either both telomeric and centromeric domains or only one domain.
RESULTS: Large duplications involving one complete domain or both domains are associated with either SRS or BWS, depending on the parental origin of the duplication. Genotype-phenotype correlation studies of partial duplications within the telomeric domain demonstrate the prominent role of IGF2, rather than H19, in the control of growth. Furthermore, it highlights the role of CDKN1C within the centromeric domain and suggests that the expected overexpression of KCNQ1OT1 from the paternal allele (in partial paternal duplications, excluding CDKN1C) does not affect the expression of CDKN1C.
CONCLUSIONS: The phenotype associated with 11p15 duplications depends on the size, genetic content, parental inheritance and imprinting status. Identification of these rare duplications is crucial for genetic counselling. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  11p15 Duplication; Beckwith-wiedemann Syndrome; Cnv; Imprinting Disorder; Silver Russell Syndrome

Mesh:

Substances:

Year:  2017        PMID: 29223973     DOI: 10.1136/jmedgenet-2017-104919

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  14 in total

1.  Ongoing Challenges in the Diagnosis of 11p15.5-Associated Imprinting Disorders.

Authors:  Deborah J G Mackay; I Karen Temple
Journal:  Mol Diagn Ther       Date:  2022-05-06       Impact factor: 4.074

Review 2.  Overgrowth syndromes - clinical and molecular aspects and tumour risk.

Authors:  Frédéric Brioude; Annick Toutain; Eloise Giabicani; Edouard Cottereau; Valérie Cormier-Daire; Irene Netchine
Journal:  Nat Rev Endocrinol       Date:  2019-05       Impact factor: 43.330

Review 3.  New Horizons in Short Children Born Small for Gestational Age.

Authors:  Irène Netchine; Manouk van der Steen; Abel López-Bermejo; Ekaterina Koledova; Mohamad Maghnie
Journal:  Front Pediatr       Date:  2021-05-13       Impact factor: 3.418

4.  The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome.

Authors:  Natali S Sobel Naveh; Daniel F Deegan; Jacklyn Huhn; Emily Traxler; Yemin Lan; Rosanna Weksberg; Arupa Ganguly; Nora Engel; Jennifer M Kalish
Journal:  Nucleic Acids Res       Date:  2021-06-21       Impact factor: 16.971

5.  A Beckwith-Wiedemann syndrome case with de novo 24 Mb duplication of chromosome 11p15.5p14.3.

Authors:  Huling Jiang; Zepeng Ping; Jianguo Wang; Xiaodan Liu; Yuxia Jin; Suping Li; Chiyan Zhou; Pinghua Huang; Yi Jin; Ling Ai; Jie Chen
Journal:  Mol Cytogenet       Date:  2021-03-03       Impact factor: 2.009

6.  Interpretation challenge of small copy number variations in the imprinting regions.

Authors:  Yi Ning; Megan Czekalski; Sylvia Herrada; Carol Greene
Journal:  Mol Genet Genomic Med       Date:  2022-04-28       Impact factor: 2.473

Review 7.  Celebrities in the heart, strangers in the pancreatic beta cell: Voltage-gated potassium channels Kv 7.1 and Kv 11.1 bridge long QT syndrome with hyperinsulinaemia as well as type 2 diabetes.

Authors:  Anniek F Lubberding; Christian R Juhl; Emil Z Skovhøj; Jørgen K Kanters; Thomas Mandrup-Poulsen; Signe S Torekov
Journal:  Acta Physiol (Oxf)       Date:  2022-01-22       Impact factor: 7.523

8.  De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia.

Authors:  Gabriel C Dworschak; Hartmut Engels; Jessica Becker; Lukas Soellner; Thomas Eggermann; Florian Kipfmueller; Andreas Müller; Heiko Reutter; Martina Kreiß
Journal:  Front Pediatr       Date:  2018-04-25       Impact factor: 3.418

Review 9.  Genetic and Epigenetic Control of CDKN1C Expression: Importance in Cell Commitment and Differentiation, Tissue Homeostasis and Human Diseases.

Authors:  Emanuela Stampone; Ilaria Caldarelli; Alberto Zullo; Debora Bencivenga; Francesco Paolo Mancini; Fulvio Della Ragione; Adriana Borriello
Journal:  Int J Mol Sci       Date:  2018-04-02       Impact factor: 5.923

10.  Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome.

Authors:  Carla Eßinger; Stephanie Karch; Ute Moog; György Fekete; Anna Lengyel; Eva Pinti; Thomas Eggermann; Matthias Begemann
Journal:  Clin Epigenetics       Date:  2020-05-11       Impact factor: 6.551

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