Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
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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Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effectsinactivation spreadlate replicationX chromosomeX‐autosome 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‐ 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‐ autosome translocation chromosome inactivation |
topic |
inactivation spread late replication X chromosome X‐ 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 |
|
_version_ |
1808129138329911296 |