Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects

Detalhes bibliográficos
Autor(a) principal: Favilla, Bianca Pereira
Data de Publicação: 2021
Outros Autores: Meloni, Vera Ayres, Perez, Ana Beatriz, Moretti-Ferreira, Danilo [UNESP], Souza, Deise Helena de [UNESP], Bellucco, Fernanda Teixeira, Melaragno, Maria Isabel
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/ajmg.a.62228
http://hdl.handle.net/11449/209362
Resumo: Patients with unbalanced X-autosome translocations are rare and usually present a skewed X-chromosome inactivation (XCI) pattern, with the derivative chromosome being preferentially inactivated, and with a possible spread of XCI into the autosomal regions attached to it, which can inactivate autosomal genes and affect the patients' phenotype. We describe three patients carrying different unbalanced X-autosome translocations, confirmed by G-banding karyotype and array techniques. We analyzed their XCI pattern and inactivation spread into autosomal regions, through HUMARA, ZDHHC15 gene assay and the novel 5-ethynyl-2 '-deoxyuridine (EdU) incorporation assay, and identified an extremely skewed XCI pattern toward the derivative chromosomes for all the patients, and a variable pattern of late-replication on the autosomal regions of the derivative chromosomes. All patients showed phenotypical overlap with patients presenting deletions of the autosomal late-replicating regions, suggesting that the inactivation of autosomal segments may be responsible for their phenotype. Our data highlight the importance of the XCI spread into autosomal regions for establishing the clinical picture in patients carrying unbalanced X-autosome translocations, and the incorporation of EdU as a novel and precise tool to evaluate the inactivation status in such patients.
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spelling Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effectsinactivation spreadlate replicationX chromosomeX&#8208autosome translocationchromosome inactivationPatients with unbalanced X-autosome translocations are rare and usually present a skewed X-chromosome inactivation (XCI) pattern, with the derivative chromosome being preferentially inactivated, and with a possible spread of XCI into the autosomal regions attached to it, which can inactivate autosomal genes and affect the patients' phenotype. We describe three patients carrying different unbalanced X-autosome translocations, confirmed by G-banding karyotype and array techniques. We analyzed their XCI pattern and inactivation spread into autosomal regions, through HUMARA, ZDHHC15 gene assay and the novel 5-ethynyl-2 '-deoxyuridine (EdU) incorporation assay, and identified an extremely skewed XCI pattern toward the derivative chromosomes for all the patients, and a variable pattern of late-replication on the autosomal regions of the derivative chromosomes. All patients showed phenotypical overlap with patients presenting deletions of the autosomal late-replicating regions, suggesting that the inactivation of autosomal segments may be responsible for their phenotype. Our data highlight the importance of the XCI spread into autosomal regions for establishing the clinical picture in patients carrying unbalanced X-autosome translocations, and the incorporation of EdU as a novel and precise tool to evaluate the inactivation status in such patients.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)UNIFESP Univ Fed Sao Paulo, Dept Morphol & Genet, Sao Paulo, BrazilUNESP Univ Estadual Paulista, Biosci Inst, Dept Chem & Biol Sci, Botucatu, SP, BrazilUNESP Univ Estadual Paulista, Biosci Inst, Dept Chem & Biol Sci, Botucatu, SP, BrazilFAPESP: 2014/11572-8FAPESP: 2019/21644-0Wiley-BlackwellUniversidade Federal de São Paulo (UNIFESP)Universidade Estadual Paulista (Unesp)Favilla, Bianca PereiraMeloni, Vera AyresPerez, Ana BeatrizMoretti-Ferreira, Danilo [UNESP]Souza, Deise Helena de [UNESP]Bellucco, Fernanda TeixeiraMelaragno, Maria Isabel2021-06-25T11:57:30Z2021-06-25T11:57:30Z2021-04-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11http://dx.doi.org/10.1002/ajmg.a.62228American Journal Of Medical Genetics Part A. Hoboken: Wiley, 11 p., 2021.1552-4825http://hdl.handle.net/11449/20936210.1002/ajmg.a.62228WOS:000645126600001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAmerican Journal Of Medical Genetics Part Ainfo:eu-repo/semantics/openAccess2021-10-23T19:28:03Zoai:repositorio.unesp.br:11449/209362Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:54:31.881960Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
title Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
spellingShingle Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
Favilla, Bianca Pereira
inactivation spread
late replication
X chromosome
X&#8208
autosome translocation
chromosome inactivation
title_short Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
title_full Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
title_fullStr Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
title_full_unstemmed Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
title_sort Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
author Favilla, Bianca Pereira
author_facet Favilla, Bianca Pereira
Meloni, Vera Ayres
Perez, Ana Beatriz
Moretti-Ferreira, Danilo [UNESP]
Souza, Deise Helena de [UNESP]
Bellucco, Fernanda Teixeira
Melaragno, Maria Isabel
author_role author
author2 Meloni, Vera Ayres
Perez, Ana Beatriz
Moretti-Ferreira, Danilo [UNESP]
Souza, Deise Helena de [UNESP]
Bellucco, Fernanda Teixeira
Melaragno, Maria Isabel
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Favilla, Bianca Pereira
Meloni, Vera Ayres
Perez, Ana Beatriz
Moretti-Ferreira, Danilo [UNESP]
Souza, Deise Helena de [UNESP]
Bellucco, Fernanda Teixeira
Melaragno, Maria Isabel
dc.subject.por.fl_str_mv inactivation spread
late replication
X chromosome
X&#8208
autosome translocation
chromosome inactivation
topic inactivation spread
late replication
X chromosome
X&#8208
autosome translocation
chromosome inactivation
description Patients with unbalanced X-autosome translocations are rare and usually present a skewed X-chromosome inactivation (XCI) pattern, with the derivative chromosome being preferentially inactivated, and with a possible spread of XCI into the autosomal regions attached to it, which can inactivate autosomal genes and affect the patients' phenotype. We describe three patients carrying different unbalanced X-autosome translocations, confirmed by G-banding karyotype and array techniques. We analyzed their XCI pattern and inactivation spread into autosomal regions, through HUMARA, ZDHHC15 gene assay and the novel 5-ethynyl-2 '-deoxyuridine (EdU) incorporation assay, and identified an extremely skewed XCI pattern toward the derivative chromosomes for all the patients, and a variable pattern of late-replication on the autosomal regions of the derivative chromosomes. All patients showed phenotypical overlap with patients presenting deletions of the autosomal late-replicating regions, suggesting that the inactivation of autosomal segments may be responsible for their phenotype. Our data highlight the importance of the XCI spread into autosomal regions for establishing the clinical picture in patients carrying unbalanced X-autosome translocations, and the incorporation of EdU as a novel and precise tool to evaluate the inactivation status in such patients.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:57:30Z
2021-06-25T11:57:30Z
2021-04-29
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1002/ajmg.a.62228
American Journal Of Medical Genetics Part A. Hoboken: Wiley, 11 p., 2021.
1552-4825
http://hdl.handle.net/11449/209362
10.1002/ajmg.a.62228
WOS:000645126600001
url http://dx.doi.org/10.1002/ajmg.a.62228
http://hdl.handle.net/11449/209362
identifier_str_mv American Journal Of Medical Genetics Part A. Hoboken: Wiley, 11 p., 2021.
1552-4825
10.1002/ajmg.a.62228
WOS:000645126600001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv American Journal Of Medical Genetics Part A
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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