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

Detalhes bibliográficos
Autor(a) principal: Castelli, Erick C. [UNESP]
Data de Publicação: 2023
Outros Autores: Paes, Gabriela Sato [UNESP], da Silva, Isabelle Mira [UNESP], Moreau, Philippe, Donadi, Eduardo A.
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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spelling 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
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