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5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints

SIMPLE SUMMARY: Large genomic rearrangements in BRCA1 consisting of deletions/duplications of one or several exons are complex events, often occurring in the 5′ region. We characterized 10 events in 20 families: one large triplication classified as benign and nine large deletions classified as patho...

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Autores principales: Caputo, Sandrine M., Telly, Dominique, Briaux, Adrien, Sesen, Julie, Ceppi, Maurizio, Bonnet, Françoise, Bourdon, Violaine, Coulet, Florence, Castera, Laurent, Delnatte, Capucine, Hardouin, Agnès, Mazoyer, Sylvie, Schultz, Inès, Sevenet, Nicolas, Uhrhammer, Nancy, Bonnet, Céline, Tilkin-Mariamé, Anne-Françoise, Houdayer, Claude, Moncoutier, Virginie, Andrieu, Catherine, Bièche, Ivan, Stern, Marc-Henri, Stoppa-Lyonnet, Dominique, Lidereau, Rosette, Toulas, Christine, Rouleau, Etienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268747/
https://www.ncbi.nlm.nih.gov/pubmed/34202044
http://dx.doi.org/10.3390/cancers13133171
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author Caputo, Sandrine M.
Telly, Dominique
Briaux, Adrien
Sesen, Julie
Ceppi, Maurizio
Bonnet, Françoise
Bourdon, Violaine
Coulet, Florence
Castera, Laurent
Delnatte, Capucine
Hardouin, Agnès
Mazoyer, Sylvie
Schultz, Inès
Sevenet, Nicolas
Uhrhammer, Nancy
Bonnet, Céline
Tilkin-Mariamé, Anne-Françoise
Houdayer, Claude
Moncoutier, Virginie
Andrieu, Catherine
Bièche, Ivan
Stern, Marc-Henri
Stoppa-Lyonnet, Dominique
Lidereau, Rosette
Toulas, Christine
Rouleau, Etienne
author_facet Caputo, Sandrine M.
Telly, Dominique
Briaux, Adrien
Sesen, Julie
Ceppi, Maurizio
Bonnet, Françoise
Bourdon, Violaine
Coulet, Florence
Castera, Laurent
Delnatte, Capucine
Hardouin, Agnès
Mazoyer, Sylvie
Schultz, Inès
Sevenet, Nicolas
Uhrhammer, Nancy
Bonnet, Céline
Tilkin-Mariamé, Anne-Françoise
Houdayer, Claude
Moncoutier, Virginie
Andrieu, Catherine
Bièche, Ivan
Stern, Marc-Henri
Stoppa-Lyonnet, Dominique
Lidereau, Rosette
Toulas, Christine
Rouleau, Etienne
author_sort Caputo, Sandrine M.
collection PubMed
description SIMPLE SUMMARY: Large genomic rearrangements in BRCA1 consisting of deletions/duplications of one or several exons are complex events, often occurring in the 5′ region. We characterized 10 events in 20 families: one large triplication classified as benign and nine large deletions classified as pathogenic. The breakpoint localization will certainly help to further understand the chromatin structure in regions sensitive to rearrangement. ABSTRACT: Background: Large genomic rearrangements (LGR) in BRCA1 consisting of deletions/duplications of one or several exons have been found throughout the gene with a large proportion occurring in the 5′ region from the promoter to exon 2. The aim of this study was to better characterize those LGR in French high-risk breast/ovarian cancer families. Methods: DNA from 20 families with one apparent duplication and nine deletions was analyzed with a dedicated comparative genomic hybridization (CGH) array, high-resolution BRCA1 Genomic Morse Codes analysis and Sanger sequencing. Results: The apparent duplication was in fact a tandem triplication of exons 1 and 2 and part of intron 2 of BRCA1, fully characterized here for the first time. We calculated a causality score with the multifactorial model from data obtained from six families, classifying this variant as benign. Among the nine deletions detected in this region, eight have never been identified. The breakpoints fell in six recurrent regions and could confirm some specific conformation of the chromatin. Conclusions: Taken together, our results firmly establish that the BRCA1 5′ region is a frequent site of different LGRs and highlight the importance of the segmental duplication and Alu sequences, particularly the very high homologous region, in the mechanism of a recombination event. This also confirmed that those events are not systematically deleterious.
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spelling pubmed-82687472021-07-10 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints Caputo, Sandrine M. Telly, Dominique Briaux, Adrien Sesen, Julie Ceppi, Maurizio Bonnet, Françoise Bourdon, Violaine Coulet, Florence Castera, Laurent Delnatte, Capucine Hardouin, Agnès Mazoyer, Sylvie Schultz, Inès Sevenet, Nicolas Uhrhammer, Nancy Bonnet, Céline Tilkin-Mariamé, Anne-Françoise Houdayer, Claude Moncoutier, Virginie Andrieu, Catherine Bièche, Ivan Stern, Marc-Henri Stoppa-Lyonnet, Dominique Lidereau, Rosette Toulas, Christine Rouleau, Etienne Cancers (Basel) Article SIMPLE SUMMARY: Large genomic rearrangements in BRCA1 consisting of deletions/duplications of one or several exons are complex events, often occurring in the 5′ region. We characterized 10 events in 20 families: one large triplication classified as benign and nine large deletions classified as pathogenic. The breakpoint localization will certainly help to further understand the chromatin structure in regions sensitive to rearrangement. ABSTRACT: Background: Large genomic rearrangements (LGR) in BRCA1 consisting of deletions/duplications of one or several exons have been found throughout the gene with a large proportion occurring in the 5′ region from the promoter to exon 2. The aim of this study was to better characterize those LGR in French high-risk breast/ovarian cancer families. Methods: DNA from 20 families with one apparent duplication and nine deletions was analyzed with a dedicated comparative genomic hybridization (CGH) array, high-resolution BRCA1 Genomic Morse Codes analysis and Sanger sequencing. Results: The apparent duplication was in fact a tandem triplication of exons 1 and 2 and part of intron 2 of BRCA1, fully characterized here for the first time. We calculated a causality score with the multifactorial model from data obtained from six families, classifying this variant as benign. Among the nine deletions detected in this region, eight have never been identified. The breakpoints fell in six recurrent regions and could confirm some specific conformation of the chromatin. Conclusions: Taken together, our results firmly establish that the BRCA1 5′ region is a frequent site of different LGRs and highlight the importance of the segmental duplication and Alu sequences, particularly the very high homologous region, in the mechanism of a recombination event. This also confirmed that those events are not systematically deleterious. MDPI 2021-06-25 /pmc/articles/PMC8268747/ /pubmed/34202044 http://dx.doi.org/10.3390/cancers13133171 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Caputo, Sandrine M.
Telly, Dominique
Briaux, Adrien
Sesen, Julie
Ceppi, Maurizio
Bonnet, Françoise
Bourdon, Violaine
Coulet, Florence
Castera, Laurent
Delnatte, Capucine
Hardouin, Agnès
Mazoyer, Sylvie
Schultz, Inès
Sevenet, Nicolas
Uhrhammer, Nancy
Bonnet, Céline
Tilkin-Mariamé, Anne-Françoise
Houdayer, Claude
Moncoutier, Virginie
Andrieu, Catherine
Bièche, Ivan
Stern, Marc-Henri
Stoppa-Lyonnet, Dominique
Lidereau, Rosette
Toulas, Christine
Rouleau, Etienne
5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title_full 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title_fullStr 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title_full_unstemmed 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title_short 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
title_sort 5′ region large genomic rearrangements in the brca1 gene in french families: identification of a tandem triplication and nine distinct deletions with five recurrent breakpoints
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268747/
https://www.ncbi.nlm.nih.gov/pubmed/34202044
http://dx.doi.org/10.3390/cancers13133171
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