The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s00251-023-01297-6 http://hdl.handle.net/11449/249044 |
Resumo: | The physiological expression of HLA-G is mainly observed in the placenta, playing an essential role in maternal–fetal tolerance. Among the HLA-G mRNA alternative transcripts, the one lacking 92 bases at the HLA-G 3′ untranslated region (3′UTR), the 92bDel transcript, is more stable, is associated with increased HLA-G soluble levels, and was observed in individuals presenting a 14 bp insertion (14 bp+) at the 3′UTR. We investigated the presence of the 92bDel transcript in placenta samples, correlating its expression levels with the HLA-G polymorphisms at the 3′UTR. The 14 bp+ allele correlates with the presence of the 92bDel transcript. However, the polymorphism triggering this alternative splicing is the + 3010/C allele (rs1710, allele C). Most 14 bp+ haplotypes (UTR-2/-5/-7) present allele + 3010/C. However, 14 bp− haplotypes such as UTR-3 are also associated with + 3010/C, and the 92bDel transcript can be detected in homozygous samples for the 14 bp- allele carrying at least one copy of UTR-3. The UTR-3 haplotype is associated with alleles G*01:04 and the HLA-G lineage HG0104, which is a high-expressing lineage. The only HLA-G lineage that is not likely to produce this transcript is HG010101, associated with the + 3010/G allele. This functional difference may be advantageous, considering the high worldwide frequency of the HG010101 lineage. Therefore, HLA-G lineages are functionally distinct regarding the 92bDel transcript expression, and the 3010/C allele triggers the alternative splicing that produces this shorter and more stable transcript. |
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The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides3′UTR92 base deletionAlternative splicingAlternative transcriptExpressionHLA-GPolymorphismThe physiological expression of HLA-G is mainly observed in the placenta, playing an essential role in maternal–fetal tolerance. Among the HLA-G mRNA alternative transcripts, the one lacking 92 bases at the HLA-G 3′ untranslated region (3′UTR), the 92bDel transcript, is more stable, is associated with increased HLA-G soluble levels, and was observed in individuals presenting a 14 bp insertion (14 bp+) at the 3′UTR. We investigated the presence of the 92bDel transcript in placenta samples, correlating its expression levels with the HLA-G polymorphisms at the 3′UTR. The 14 bp+ allele correlates with the presence of the 92bDel transcript. However, the polymorphism triggering this alternative splicing is the + 3010/C allele (rs1710, allele C). Most 14 bp+ haplotypes (UTR-2/-5/-7) present allele + 3010/C. However, 14 bp− haplotypes such as UTR-3 are also associated with + 3010/C, and the 92bDel transcript can be detected in homozygous samples for the 14 bp- allele carrying at least one copy of UTR-3. The UTR-3 haplotype is associated with alleles G*01:04 and the HLA-G lineage HG0104, which is a high-expressing lineage. The only HLA-G lineage that is not likely to produce this transcript is HG010101, associated with the + 3010/G allele. This functional difference may be advantageous, considering the high worldwide frequency of the HG010101 lineage. Therefore, HLA-G lineages are functionally distinct regarding the 92bDel transcript expression, and the 3010/C allele triggers the alternative splicing that produces this shorter and more stable transcript.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Pathology School of Medicine São Paulo State University (Unesp)Molecular Genetics and Bioinformatics Laboratory (GeMBio) – Experimental Research Unit School of Medicine São Paulo State University (Unesp)Commissariat À L’Energie Atomique Et Aux Energies Alternatives Direction de La Recherche Fondamentale Institut de Biologie François Jacob Service de Recherches en Hémato-ImmunologieHôpital Saint-LouisU976 HIPI Unit ISRL Université Paris CitéDivision of Clinical Immunology Department of Medicine Ribeirão Preto Medical School University of São Paulo (USP), SP, CEPDepartment of Pathology School of Medicine São Paulo State University (Unesp)Molecular Genetics and Bioinformatics Laboratory (GeMBio) – Experimental Research Unit School of Medicine São Paulo State University (Unesp)FAPESP: 13/17084-2FAPESP: 17/14345-0Universidade Estadual Paulista (UNESP)Service de Recherches en Hémato-ImmunologieHôpital Saint-LouisUniversité Paris CitéUniversidade de São Paulo (USP)Castelli, Erick C. [UNESP]Paes, Gabriela Sato [UNESP]da Silva, Isabelle Mira [UNESP]Moreau, PhilippeDonadi, Eduardo A.2023-07-29T14:00:56Z2023-07-29T14:00:56Z2023-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article155-160http://dx.doi.org/10.1007/s00251-023-01297-6Immunogenetics, v. 75, n. 2, p. 155-160, 2023.1432-12110093-7711http://hdl.handle.net/11449/24904410.1007/s00251-023-01297-62-s2.0-85149281004Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengImmunogeneticsinfo:eu-repo/semantics/openAccess2023-07-29T14:00:56Zoai:repositorio.unesp.br:11449/249044Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:59:23.447875Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
title |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
spellingShingle |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides Castelli, Erick C. [UNESP] 3′UTR 92 base deletion Alternative splicing Alternative transcript Expression HLA-G Polymorphism |
title_short |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
title_full |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
title_fullStr |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
title_full_unstemmed |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
title_sort |
The + 3010/C single nucleotide polymorphism (rs1710) at the HLA-G 3′ untranslated region is associated with a short transcript exhibiting a deletion of 92 nucleotides |
author |
Castelli, Erick C. [UNESP] |
author_facet |
Castelli, Erick C. [UNESP] Paes, Gabriela Sato [UNESP] da Silva, Isabelle Mira [UNESP] Moreau, Philippe Donadi, Eduardo A. |
author_role |
author |
author2 |
Paes, Gabriela Sato [UNESP] da Silva, Isabelle Mira [UNESP] Moreau, Philippe Donadi, Eduardo A. |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Service de Recherches en Hémato-ImmunologieHôpital Saint-Louis Université Paris Cité Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Castelli, Erick C. [UNESP] Paes, Gabriela Sato [UNESP] da Silva, Isabelle Mira [UNESP] Moreau, Philippe Donadi, Eduardo A. |
dc.subject.por.fl_str_mv |
3′UTR 92 base deletion Alternative splicing Alternative transcript Expression HLA-G Polymorphism |
topic |
3′UTR 92 base deletion Alternative splicing Alternative transcript Expression HLA-G Polymorphism |
description |
The physiological expression of HLA-G is mainly observed in the placenta, playing an essential role in maternal–fetal tolerance. Among the HLA-G mRNA alternative transcripts, the one lacking 92 bases at the HLA-G 3′ untranslated region (3′UTR), the 92bDel transcript, is more stable, is associated with increased HLA-G soluble levels, and was observed in individuals presenting a 14 bp insertion (14 bp+) at the 3′UTR. We investigated the presence of the 92bDel transcript in placenta samples, correlating its expression levels with the HLA-G polymorphisms at the 3′UTR. The 14 bp+ allele correlates with the presence of the 92bDel transcript. However, the polymorphism triggering this alternative splicing is the + 3010/C allele (rs1710, allele C). Most 14 bp+ haplotypes (UTR-2/-5/-7) present allele + 3010/C. However, 14 bp− haplotypes such as UTR-3 are also associated with + 3010/C, and the 92bDel transcript can be detected in homozygous samples for the 14 bp- allele carrying at least one copy of UTR-3. The UTR-3 haplotype is associated with alleles G*01:04 and the HLA-G lineage HG0104, which is a high-expressing lineage. The only HLA-G lineage that is not likely to produce this transcript is HG010101, associated with the + 3010/G allele. This functional difference may be advantageous, considering the high worldwide frequency of the HG010101 lineage. Therefore, HLA-G lineages are functionally distinct regarding the 92bDel transcript expression, and the 3010/C allele triggers the alternative splicing that produces this shorter and more stable transcript. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T14:00:56Z 2023-07-29T14:00:56Z 2023-04-01 |
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/10.1007/s00251-023-01297-6 Immunogenetics, v. 75, n. 2, p. 155-160, 2023. 1432-1211 0093-7711 http://hdl.handle.net/11449/249044 10.1007/s00251-023-01297-6 2-s2.0-85149281004 |
url |
http://dx.doi.org/10.1007/s00251-023-01297-6 http://hdl.handle.net/11449/249044 |
identifier_str_mv |
Immunogenetics, v. 75, n. 2, p. 155-160, 2023. 1432-1211 0093-7711 10.1007/s00251-023-01297-6 2-s2.0-85149281004 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Immunogenetics |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
155-160 |
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_ |
1808128301504397312 |