Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome

Detalhes bibliográficos
Autor(a) principal: Corrêa, Thiago
Data de Publicação: 2018
Outros Autores: Mergener, Rafaella, Leite, Júlio César Loguercio, Galera, Marcial Francis, Moreira, Lília Maria de Azevedo, Vargas, José Eduardo, Riegel, Mariluce
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/181591
Resumo: Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene deletion syndrome involving variable size deletions. In this study, we perform a cytogenomic integrative analysis combining classical cytogenetic methods, fluorescence in situ hybridization (FISH), chromosomal microarray analysis (CMA), and systems biology strategies, to establish the cytogenomic profile involving the 4p16.3 critical region and suggest WHS-related intracellular cell signaling cascades. The cytogenetic and clinical patient profiles were evaluated. We characterized 12 terminal deletions, one interstitial deletion, two ring chromosomes, and one classical translocation 4;8.CMAallowed delineation of the deletions, which ranged from3.7 to 25.6Mb with breakpoints from 4p16.3 to 4p15.33. Furthermore, the smallest region of overlapping (SRO) encompassed seven genes in a terminal region of 330 kb in the 4p16.3 region, suggesting a region of susceptibility to convulsions and microcephaly. Therefore, molecular interaction networks and topological analysis were performed to understand these WHS-related symptoms. Our results suggest that specific cell signaling pathways including dopamine receptor,NAD+nucleosidase activity, and fibroblast growth factoractivated receptor activity are associated with the diverse pathological WHS phenotypes and their symptoms. Additionally, we identified 29 hub-bottlenecks (H-B) nodes with a major role in WHS.
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spelling Corrêa, ThiagoMergener, RafaellaLeite, Júlio César LoguercioGalera, Marcial FrancisMoreira, Lília Maria de AzevedoVargas, José EduardoRiegel, Mariluce2018-09-01T02:55:15Z20182314-6141http://hdl.handle.net/10183/181591001067565Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene deletion syndrome involving variable size deletions. In this study, we perform a cytogenomic integrative analysis combining classical cytogenetic methods, fluorescence in situ hybridization (FISH), chromosomal microarray analysis (CMA), and systems biology strategies, to establish the cytogenomic profile involving the 4p16.3 critical region and suggest WHS-related intracellular cell signaling cascades. The cytogenetic and clinical patient profiles were evaluated. We characterized 12 terminal deletions, one interstitial deletion, two ring chromosomes, and one classical translocation 4;8.CMAallowed delineation of the deletions, which ranged from3.7 to 25.6Mb with breakpoints from 4p16.3 to 4p15.33. Furthermore, the smallest region of overlapping (SRO) encompassed seven genes in a terminal region of 330 kb in the 4p16.3 region, suggesting a region of susceptibility to convulsions and microcephaly. Therefore, molecular interaction networks and topological analysis were performed to understand these WHS-related symptoms. Our results suggest that specific cell signaling pathways including dopamine receptor,NAD+nucleosidase activity, and fibroblast growth factoractivated receptor activity are associated with the diverse pathological WHS phenotypes and their symptoms. Additionally, we identified 29 hub-bottlenecks (H-B) nodes with a major role in WHS.application/pdfengBiomed research international. New York. Vol. 2018 2018), ID 5436187, 10 p.Síndrome de Wolf-HirschhornAnálise citogenéticaCromossomos humanos par 4Receptores dopaminérgicosFenótipoVariação biológica da populaçãoCytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn SyndromeEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001067565.pdfTexto completo (inglês)application/pdf2089036http://www.lume.ufrgs.br/bitstream/10183/181591/1/001067565.pdf32f03f5e87aca3ede153a761aca51b1dMD51TEXT001067565.pdf.txt001067565.pdf.txtExtracted Texttext/plain41835http://www.lume.ufrgs.br/bitstream/10183/181591/2/001067565.pdf.txt9f60af736c172bc231242f7a8864e9cdMD52THUMBNAIL001067565.pdf.jpg001067565.pdf.jpgGenerated Thumbnailimage/jpeg1817http://www.lume.ufrgs.br/bitstream/10183/181591/3/001067565.pdf.jpg86ae8c96233cc84abf2a8e8759093990MD5310183/1815912023-04-20 03:22:11.59944oai:www.lume.ufrgs.br:10183/181591Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-04-20T06:22:11Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
title Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
spellingShingle Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
Corrêa, Thiago
Síndrome de Wolf-Hirschhorn
Análise citogenética
Cromossomos humanos par 4
Receptores dopaminérgicos
Fenótipo
Variação biológica da população
title_short Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
title_full Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
title_fullStr Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
title_full_unstemmed Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
title_sort Cytogenomic integrative network analysis of the critical region associated with Wolf-Hirschhorn Syndrome
author Corrêa, Thiago
author_facet Corrêa, Thiago
Mergener, Rafaella
Leite, Júlio César Loguercio
Galera, Marcial Francis
Moreira, Lília Maria de Azevedo
Vargas, José Eduardo
Riegel, Mariluce
author_role author
author2 Mergener, Rafaella
Leite, Júlio César Loguercio
Galera, Marcial Francis
Moreira, Lília Maria de Azevedo
Vargas, José Eduardo
Riegel, Mariluce
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Corrêa, Thiago
Mergener, Rafaella
Leite, Júlio César Loguercio
Galera, Marcial Francis
Moreira, Lília Maria de Azevedo
Vargas, José Eduardo
Riegel, Mariluce
dc.subject.por.fl_str_mv Síndrome de Wolf-Hirschhorn
Análise citogenética
Cromossomos humanos par 4
Receptores dopaminérgicos
Fenótipo
Variação biológica da população
topic Síndrome de Wolf-Hirschhorn
Análise citogenética
Cromossomos humanos par 4
Receptores dopaminérgicos
Fenótipo
Variação biológica da população
description Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene deletion syndrome involving variable size deletions. In this study, we perform a cytogenomic integrative analysis combining classical cytogenetic methods, fluorescence in situ hybridization (FISH), chromosomal microarray analysis (CMA), and systems biology strategies, to establish the cytogenomic profile involving the 4p16.3 critical region and suggest WHS-related intracellular cell signaling cascades. The cytogenetic and clinical patient profiles were evaluated. We characterized 12 terminal deletions, one interstitial deletion, two ring chromosomes, and one classical translocation 4;8.CMAallowed delineation of the deletions, which ranged from3.7 to 25.6Mb with breakpoints from 4p16.3 to 4p15.33. Furthermore, the smallest region of overlapping (SRO) encompassed seven genes in a terminal region of 330 kb in the 4p16.3 region, suggesting a region of susceptibility to convulsions and microcephaly. Therefore, molecular interaction networks and topological analysis were performed to understand these WHS-related symptoms. Our results suggest that specific cell signaling pathways including dopamine receptor,NAD+nucleosidase activity, and fibroblast growth factoractivated receptor activity are associated with the diverse pathological WHS phenotypes and their symptoms. Additionally, we identified 29 hub-bottlenecks (H-B) nodes with a major role in WHS.
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