HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , |
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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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:29462024-08-05T19:50:30.542883Repositório 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 |
|
_version_ |
1808129127347126272 |