HLA-G UTR haplotype conservation in the Malian population: association with soluble HLA-G

The HLA-G molecule plays an important role in immunomodulation. In a previous study carried out on a southern French population our team showed that HLA-G haplotypes, defined by SNPs in the coding region and specific SNPs located in 5'URR and 3'UTR regulatory regions, are associated with d...

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Veröffentlicht in:PloS one 2013-12, Vol.8 (12), p.e82517-e82517
Hauptverfasser: Carlini, Federico, Traore, Karim, Cherouat, Nissem, Roubertoux, Pierre, Buhler, Stéphane, Cortey, Martì, Simon, Sophie, Doumbo, Ogobara, Chiaroni, Jacques, Picard, Christophe, Di Cristofaro, Julie
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container_title PloS one
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creator Carlini, Federico
Traore, Karim
Cherouat, Nissem
Roubertoux, Pierre
Buhler, Stéphane
Cortey, Martì
Simon, Sophie
Doumbo, Ogobara
Chiaroni, Jacques
Picard, Christophe
Di Cristofaro, Julie
description The HLA-G molecule plays an important role in immunomodulation. In a previous study carried out on a southern French population our team showed that HLA-G haplotypes, defined by SNPs in the coding region and specific SNPs located in 5'URR and 3'UTR regulatory regions, are associated with differential soluble HLA-G expression (sHLA-G). Furthermore, the structure of these HLA-G haplotypes appears to be conserved in geographically distant populations. The aim of our study is to confirm these expectations in a sub-Saharan African population and to explore additional factors, such as HLA-A alleles, that might influence sHLA-G expression. DNA and plasma samples were collected from 229 Malians; HLA-G and HLA-A genotyping were respectively performed by the Snap Shot® method and by Luminex™ technology. sHLA-G dosage was performed using an ELISA kit. HLA-G and HLA-A allelic and haplotypic frequencies were estimated using an EM algorithm from the Gene[Rate] program. Associations between genetic and non genetic parameters with sHLA-G were performed using a non-parametric test with GRAPH PAD Prism 5. Our results reveal a good conservation of the HLA-G UTR haplotype structure in populations with different origins and demographic histories. These UTR haplotypes appear to be involved in different sHLA-G expression patterns. Specifically, the UTR-2 haplotype was associated with low sHLA-G levels, displaying a dominant negative effect. Furthermore, an allelic effect of both HLA-G and HLA-A, as well as non genetic parameters, such as age and gender possibly linked to osteogenesis and sexual hormones, also seem to be involved in the modulation of sHLA-G. These data suggest that further investigation in larger cohorts and in populations from various ethnical backgrounds is necessary not only to detect new functional polymorphism in HLA-G regulatory regions, but also to reveal the extent of biological phenomena that influence sHLA-G secretion and this might therefore have an impact on transplantation practice.
doi_str_mv 10.1371/journal.pone.0082517
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In a previous study carried out on a southern French population our team showed that HLA-G haplotypes, defined by SNPs in the coding region and specific SNPs located in 5'URR and 3'UTR regulatory regions, are associated with differential soluble HLA-G expression (sHLA-G). Furthermore, the structure of these HLA-G haplotypes appears to be conserved in geographically distant populations. The aim of our study is to confirm these expectations in a sub-Saharan African population and to explore additional factors, such as HLA-A alleles, that might influence sHLA-G expression. DNA and plasma samples were collected from 229 Malians; HLA-G and HLA-A genotyping were respectively performed by the Snap Shot® method and by Luminex™ technology. sHLA-G dosage was performed using an ELISA kit. HLA-G and HLA-A allelic and haplotypic frequencies were estimated using an EM algorithm from the Gene[Rate] program. Associations between genetic and non genetic parameters with sHLA-G were performed using a non-parametric test with GRAPH PAD Prism 5. Our results reveal a good conservation of the HLA-G UTR haplotype structure in populations with different origins and demographic histories. These UTR haplotypes appear to be involved in different sHLA-G expression patterns. Specifically, the UTR-2 haplotype was associated with low sHLA-G levels, displaying a dominant negative effect. Furthermore, an allelic effect of both HLA-G and HLA-A, as well as non genetic parameters, such as age and gender possibly linked to osteogenesis and sexual hormones, also seem to be involved in the modulation of sHLA-G. These data suggest that further investigation in larger cohorts and in populations from various ethnical backgrounds is necessary not only to detect new functional polymorphism in HLA-G regulatory regions, but also to reveal the extent of biological phenomena that influence sHLA-G secretion and this might therefore have an impact on transplantation practice.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0082517</identifier><identifier>PMID: 24376542</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>3' Untranslated regions ; 3' Untranslated Regions - genetics ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Alleles ; Analysis ; Antigens ; Biocompatibility ; Biomedical materials ; Child ; Child, Preschool ; Conservation ; Conserved Sequence - genetics ; Demographics ; Dentistry ; Deoxyribonucleic acid ; DNA ; Enzyme-linked immunosorbent assay ; Epidemiology ; Female ; Gene expression ; Gene Frequency ; Genetic Loci ; Genetics ; Genotyping ; Haplotypes ; Haplotypes - genetics ; Histocompatibility antigen HLA ; HLA antigens ; HLA-A Antigens - genetics ; HLA-G Antigens - genetics ; Hormones ; Human genetics ; Humans ; Immunomodulation ; Laboratories ; Life Sciences ; Linkage Disequilibrium - genetics ; Male ; Mali ; Middle Aged ; Miscarriage ; Osteogenesis ; Parasitic diseases ; Pharmacy ; Polymorphism ; Polymorphism, Single Nucleotide - genetics ; Population ; Population genetics ; Populations ; Populations and Evolution ; Regulatory sequences ; Sex hormones ; Single-nucleotide polymorphism ; Solubility ; Studies ; Transplantation ; Transplants &amp; implants ; Young Adult</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e82517-e82517</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Carlini et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Attribution</rights><rights>2013 Carlini et al 2013 Carlini et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c726t-6cbbace62372ded5fa65abc3d71322833094c8e755bea12ca3511a5804a34c7a3</citedby><cites>FETCH-LOGICAL-c726t-6cbbace62372ded5fa65abc3d71322833094c8e755bea12ca3511a5804a34c7a3</cites><orcidid>0000-0002-3133-8990 ; 0000-0001-9118-5239 ; 0000-0001-9013-2725</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871591/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871591/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24376542$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00940846$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Caramelli, David</contributor><creatorcontrib>Carlini, Federico</creatorcontrib><creatorcontrib>Traore, Karim</creatorcontrib><creatorcontrib>Cherouat, Nissem</creatorcontrib><creatorcontrib>Roubertoux, Pierre</creatorcontrib><creatorcontrib>Buhler, Stéphane</creatorcontrib><creatorcontrib>Cortey, Martì</creatorcontrib><creatorcontrib>Simon, Sophie</creatorcontrib><creatorcontrib>Doumbo, Ogobara</creatorcontrib><creatorcontrib>Chiaroni, Jacques</creatorcontrib><creatorcontrib>Picard, Christophe</creatorcontrib><creatorcontrib>Di Cristofaro, Julie</creatorcontrib><title>HLA-G UTR haplotype conservation in the Malian population: association with soluble HLA-G</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The HLA-G molecule plays an important role in immunomodulation. In a previous study carried out on a southern French population our team showed that HLA-G haplotypes, defined by SNPs in the coding region and specific SNPs located in 5'URR and 3'UTR regulatory regions, are associated with differential soluble HLA-G expression (sHLA-G). Furthermore, the structure of these HLA-G haplotypes appears to be conserved in geographically distant populations. The aim of our study is to confirm these expectations in a sub-Saharan African population and to explore additional factors, such as HLA-A alleles, that might influence sHLA-G expression. DNA and plasma samples were collected from 229 Malians; HLA-G and HLA-A genotyping were respectively performed by the Snap Shot® method and by Luminex™ technology. sHLA-G dosage was performed using an ELISA kit. HLA-G and HLA-A allelic and haplotypic frequencies were estimated using an EM algorithm from the Gene[Rate] program. Associations between genetic and non genetic parameters with sHLA-G were performed using a non-parametric test with GRAPH PAD Prism 5. Our results reveal a good conservation of the HLA-G UTR haplotype structure in populations with different origins and demographic histories. These UTR haplotypes appear to be involved in different sHLA-G expression patterns. Specifically, the UTR-2 haplotype was associated with low sHLA-G levels, displaying a dominant negative effect. Furthermore, an allelic effect of both HLA-G and HLA-A, as well as non genetic parameters, such as age and gender possibly linked to osteogenesis and sexual hormones, also seem to be involved in the modulation of sHLA-G. These data suggest that further investigation in larger cohorts and in populations from various ethnical backgrounds is necessary not only to detect new functional polymorphism in HLA-G regulatory regions, but also to reveal the extent of biological phenomena that influence sHLA-G secretion and this might therefore have an impact on transplantation practice.</description><subject>3' Untranslated regions</subject><subject>3' Untranslated Regions - genetics</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alleles</subject><subject>Analysis</subject><subject>Antigens</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Conservation</subject><subject>Conserved Sequence - genetics</subject><subject>Demographics</subject><subject>Dentistry</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Frequency</subject><subject>Genetic Loci</subject><subject>Genetics</subject><subject>Genotyping</subject><subject>Haplotypes</subject><subject>Haplotypes - genetics</subject><subject>Histocompatibility antigen HLA</subject><subject>HLA antigens</subject><subject>HLA-A Antigens - genetics</subject><subject>HLA-G Antigens - genetics</subject><subject>Hormones</subject><subject>Human genetics</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Laboratories</subject><subject>Life Sciences</subject><subject>Linkage Disequilibrium - genetics</subject><subject>Male</subject><subject>Mali</subject><subject>Middle Aged</subject><subject>Miscarriage</subject><subject>Osteogenesis</subject><subject>Parasitic diseases</subject><subject>Pharmacy</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Population</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Populations and Evolution</subject><subject>Regulatory sequences</subject><subject>Sex hormones</subject><subject>Single-nucleotide polymorphism</subject><subject>Solubility</subject><subject>Studies</subject><subject>Transplantation</subject><subject>Transplants &amp; 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In a previous study carried out on a southern French population our team showed that HLA-G haplotypes, defined by SNPs in the coding region and specific SNPs located in 5'URR and 3'UTR regulatory regions, are associated with differential soluble HLA-G expression (sHLA-G). Furthermore, the structure of these HLA-G haplotypes appears to be conserved in geographically distant populations. The aim of our study is to confirm these expectations in a sub-Saharan African population and to explore additional factors, such as HLA-A alleles, that might influence sHLA-G expression. DNA and plasma samples were collected from 229 Malians; HLA-G and HLA-A genotyping were respectively performed by the Snap Shot® method and by Luminex™ technology. sHLA-G dosage was performed using an ELISA kit. HLA-G and HLA-A allelic and haplotypic frequencies were estimated using an EM algorithm from the Gene[Rate] program. Associations between genetic and non genetic parameters with sHLA-G were performed using a non-parametric test with GRAPH PAD Prism 5. Our results reveal a good conservation of the HLA-G UTR haplotype structure in populations with different origins and demographic histories. These UTR haplotypes appear to be involved in different sHLA-G expression patterns. Specifically, the UTR-2 haplotype was associated with low sHLA-G levels, displaying a dominant negative effect. Furthermore, an allelic effect of both HLA-G and HLA-A, as well as non genetic parameters, such as age and gender possibly linked to osteogenesis and sexual hormones, also seem to be involved in the modulation of sHLA-G. These data suggest that further investigation in larger cohorts and in populations from various ethnical backgrounds is necessary not only to detect new functional polymorphism in HLA-G regulatory regions, but also to reveal the extent of biological phenomena that influence sHLA-G secretion and this might therefore have an impact on transplantation practice.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24376542</pmid><doi>10.1371/journal.pone.0082517</doi><tpages>e82517</tpages><orcidid>https://orcid.org/0000-0002-3133-8990</orcidid><orcidid>https://orcid.org/0000-0001-9118-5239</orcidid><orcidid>https://orcid.org/0000-0001-9013-2725</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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1932-6203
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subjects 3' Untranslated regions
3' Untranslated Regions - genetics
Adolescent
Adult
Aged
Aged, 80 and over
Alleles
Analysis
Antigens
Biocompatibility
Biomedical materials
Child
Child, Preschool
Conservation
Conserved Sequence - genetics
Demographics
Dentistry
Deoxyribonucleic acid
DNA
Enzyme-linked immunosorbent assay
Epidemiology
Female
Gene expression
Gene Frequency
Genetic Loci
Genetics
Genotyping
Haplotypes
Haplotypes - genetics
Histocompatibility antigen HLA
HLA antigens
HLA-A Antigens - genetics
HLA-G Antigens - genetics
Hormones
Human genetics
Humans
Immunomodulation
Laboratories
Life Sciences
Linkage Disequilibrium - genetics
Male
Mali
Middle Aged
Miscarriage
Osteogenesis
Parasitic diseases
Pharmacy
Polymorphism
Polymorphism, Single Nucleotide - genetics
Population
Population genetics
Populations
Populations and Evolution
Regulatory sequences
Sex hormones
Single-nucleotide polymorphism
Solubility
Studies
Transplantation
Transplants & implants
Young Adult
title HLA-G UTR haplotype conservation in the Malian population: association with soluble HLA-G
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