HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus

Detalhes bibliográficos
Autor(a) principal: Castelli, Erick C. [UNESP]
Data de Publicação: 2017
Outros Autores: Gerasimou, Petroula, Paz, Michelle A. [UNESP], Ramalho, Jaqueline [UNESP], Porto, Iane O.P. [UNESP], Lima, Thálitta H.A. [UNESP], Souza, Andréia S. [UNESP], Veiga-Castelli, Luciana C., Collares, Cristhianna V.A., Donadi, Eduardo A., Mendes-Junior, Celso T., Costeas, Paul
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.molimm.2017.01.020
http://hdl.handle.net/11449/176976
Resumo: The HLA-G molecule presents immunomodulatory properties that might inhibit immune responses when interacting with specific Natural Killer and T cell receptors, such as KIR2DL4, ILT2 and ILT4. Thus, HLA-G might influence the outcome of situations in which fine immune system modulation is required, such as autoimmune diseases, transplants, cancer and pregnancy. The majority of the studies regarding the HLA-G gene variability so far was restricted to a specific gene segment (i.e., promoter, coding or 3' untranslated region), and was performed by using Sanger sequencing and probabilistic models to infer haplotypes. Here we propose a massively parallel sequencing (NGS) with a bioinformatics strategy to evaluate the entire HLA-G regulatory and coding segments, with haplotypes inferred relying more on the straightforward haplotyping capabilities of NGS, and less on probabilistic models. Then, HLA-G variability was surveyed in two admixed population samples of distinct geographical regions and demographic backgrounds, Cyprus and Brazil. Most haplotypes (promoters, coding, 3'UTR and extended ones) were detected both in Brazil and Cyprus and were identical to the ones already described by probabilistic models, indicating that these haplotypes are quite old and may be present worldwide.
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spelling HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and CyprusBrazilCyprusHaplotypesHLA-GMassive parallel sequencingNext generation sequencingNGSPolymorphismsVariabilityThe HLA-G molecule presents immunomodulatory properties that might inhibit immune responses when interacting with specific Natural Killer and T cell receptors, such as KIR2DL4, ILT2 and ILT4. Thus, HLA-G might influence the outcome of situations in which fine immune system modulation is required, such as autoimmune diseases, transplants, cancer and pregnancy. The majority of the studies regarding the HLA-G gene variability so far was restricted to a specific gene segment (i.e., promoter, coding or 3' untranslated region), and was performed by using Sanger sequencing and probabilistic models to infer haplotypes. Here we propose a massively parallel sequencing (NGS) with a bioinformatics strategy to evaluate the entire HLA-G regulatory and coding segments, with haplotypes inferred relying more on the straightforward haplotyping capabilities of NGS, and less on probabilistic models. Then, HLA-G variability was surveyed in two admixed population samples of distinct geographical regions and demographic backgrounds, Cyprus and Brazil. Most haplotypes (promoters, coding, 3'UTR and extended ones) were detected both in Brazil and Cyprus and were identical to the ones already described by probabilistic models, indicating that these haplotypes are quite old and may be present worldwide.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Pathology School of Medicine UNESP – Univ. Estadual PaulistaMolecular Genetics and Bioinformatics Laboratory Experimental Research Unit (UNIPEX) Sector 5 School of Medicine UNESP – Univ. Estadual PaulistaKaraiskakio FoundationDivision of Clinical Immunology Department of Medicine School of Medicine of Ribeirão Preto University of the State of São Paulo (USP)Departamento de Química Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São PauloDepartment of Pathology School of Medicine UNESP – Univ. Estadual PaulistaMolecular Genetics and Bioinformatics Laboratory Experimental Research Unit (UNIPEX) Sector 5 School of Medicine UNESP – Univ. Estadual PaulistaFAPESP: 2013/17084-2FAPESP: 2014/18730-8Universidade Estadual Paulista (Unesp)Karaiskakio FoundationUniversidade de São Paulo (USP)Castelli, Erick C. [UNESP]Gerasimou, PetroulaPaz, Michelle A. [UNESP]Ramalho, Jaqueline [UNESP]Porto, Iane O.P. [UNESP]Lima, Thálitta H.A. [UNESP]Souza, Andréia S. [UNESP]Veiga-Castelli, Luciana C.Collares, Cristhianna V.A.Donadi, Eduardo A.Mendes-Junior, Celso T.Costeas, Paul2018-12-11T17:23:21Z2018-12-11T17:23:21Z2017-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article115-126application/pdfhttp://dx.doi.org/10.1016/j.molimm.2017.01.020Molecular Immunology, v. 83, p. 115-126.1872-91420161-5890http://hdl.handle.net/11449/17697610.1016/j.molimm.2017.01.0202-s2.0-850107232082-s2.0-85010723208.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecular Immunology1,352info:eu-repo/semantics/openAccess2023-12-09T06:19:06Zoai:repositorio.unesp.br:11449/176976Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-09T06:19:06Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
title HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
spellingShingle HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
Castelli, Erick C. [UNESP]
Brazil
Cyprus
Haplotypes
HLA-G
Massive parallel sequencing
Next generation sequencing
NGS
Polymorphisms
Variability
title_short HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
title_full HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
title_fullStr HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
title_full_unstemmed HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
title_sort HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
author Castelli, Erick C. [UNESP]
author_facet Castelli, Erick C. [UNESP]
Gerasimou, Petroula
Paz, Michelle A. [UNESP]
Ramalho, Jaqueline [UNESP]
Porto, Iane O.P. [UNESP]
Lima, Thálitta H.A. [UNESP]
Souza, Andréia S. [UNESP]
Veiga-Castelli, Luciana C.
Collares, Cristhianna V.A.
Donadi, Eduardo A.
Mendes-Junior, Celso T.
Costeas, Paul
author_role author
author2 Gerasimou, Petroula
Paz, Michelle A. [UNESP]
Ramalho, Jaqueline [UNESP]
Porto, Iane O.P. [UNESP]
Lima, Thálitta H.A. [UNESP]
Souza, Andréia S. [UNESP]
Veiga-Castelli, Luciana C.
Collares, Cristhianna V.A.
Donadi, Eduardo A.
Mendes-Junior, Celso T.
Costeas, Paul
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Karaiskakio Foundation
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Castelli, Erick C. [UNESP]
Gerasimou, Petroula
Paz, Michelle A. [UNESP]
Ramalho, Jaqueline [UNESP]
Porto, Iane O.P. [UNESP]
Lima, Thálitta H.A. [UNESP]
Souza, Andréia S. [UNESP]
Veiga-Castelli, Luciana C.
Collares, Cristhianna V.A.
Donadi, Eduardo A.
Mendes-Junior, Celso T.
Costeas, Paul
dc.subject.por.fl_str_mv Brazil
Cyprus
Haplotypes
HLA-G
Massive parallel sequencing
Next generation sequencing
NGS
Polymorphisms
Variability
topic Brazil
Cyprus
Haplotypes
HLA-G
Massive parallel sequencing
Next generation sequencing
NGS
Polymorphisms
Variability
description The HLA-G molecule presents immunomodulatory properties that might inhibit immune responses when interacting with specific Natural Killer and T cell receptors, such as KIR2DL4, ILT2 and ILT4. Thus, HLA-G might influence the outcome of situations in which fine immune system modulation is required, such as autoimmune diseases, transplants, cancer and pregnancy. The majority of the studies regarding the HLA-G gene variability so far was restricted to a specific gene segment (i.e., promoter, coding or 3' untranslated region), and was performed by using Sanger sequencing and probabilistic models to infer haplotypes. Here we propose a massively parallel sequencing (NGS) with a bioinformatics strategy to evaluate the entire HLA-G regulatory and coding segments, with haplotypes inferred relying more on the straightforward haplotyping capabilities of NGS, and less on probabilistic models. Then, HLA-G variability was surveyed in two admixed population samples of distinct geographical regions and demographic backgrounds, Cyprus and Brazil. Most haplotypes (promoters, coding, 3'UTR and extended ones) were detected both in Brazil and Cyprus and were identical to the ones already described by probabilistic models, indicating that these haplotypes are quite old and may be present worldwide.
publishDate 2017
dc.date.none.fl_str_mv 2017-03-01
2018-12-11T17:23:21Z
2018-12-11T17:23:21Z
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/10.1016/j.molimm.2017.01.020
Molecular Immunology, v. 83, p. 115-126.
1872-9142
0161-5890
http://hdl.handle.net/11449/176976
10.1016/j.molimm.2017.01.020
2-s2.0-85010723208
2-s2.0-85010723208.pdf
url http://dx.doi.org/10.1016/j.molimm.2017.01.020
http://hdl.handle.net/11449/176976
identifier_str_mv Molecular Immunology, v. 83, p. 115-126.
1872-9142
0161-5890
10.1016/j.molimm.2017.01.020
2-s2.0-85010723208
2-s2.0-85010723208.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecular Immunology
1,352
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 115-126
application/pdf
dc.source.none.fl_str_mv Scopus
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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