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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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 & 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 & implants</subject><subject>Young 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BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carlini, Federico</au><au>Traore, Karim</au><au>Cherouat, Nissem</au><au>Roubertoux, Pierre</au><au>Buhler, Stéphane</au><au>Cortey, Martì</au><au>Simon, Sophie</au><au>Doumbo, Ogobara</au><au>Chiaroni, Jacques</au><au>Picard, Christophe</au><au>Di Cristofaro, Julie</au><au>Caramelli, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA-G UTR haplotype conservation in the Malian population: association with soluble HLA-G</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-12-23</date><risdate>2013</risdate><volume>8</volume><issue>12</issue><spage>e82517</spage><epage>e82517</epage><pages>e82517-e82517</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-12, Vol.8 (12), p.e82517-e82517 |
issn | 1932-6203 1932-6203 |
language | eng |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry |
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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