HLA-G allelic variants are associated with differences in the HLA-G mRNA isoform profile and HLA-G mRNA levels
During pregnancy, the human extra-villous trophoblast in the contact zone between maternal and fetal tissue in the placenta does not express the classical MHC class I and II molecules. Instead, HLA-G and -C, and possibly HLA-E, are expressed. HLA-G may modulate the immunological relationship between...
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Veröffentlicht in: | Immunogenetics (New York) 2003-05, Vol.55 (2), p.63-79 |
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description | During pregnancy, the human extra-villous trophoblast in the contact zone between maternal and fetal tissue in the placenta does not express the classical MHC class I and II molecules. Instead, HLA-G and -C, and possibly HLA-E, are expressed. HLA-G may modulate the immunological relationship between mother and fetus in several ways. Finally, the expression of membrane-bound HLA-G and soluble HLA-G has been proposed to influence the outcome of pregnancy, and an aberrant HLA-G expression in pre-eclamptic placentas and spontaneous abortions has been reported. Here, an association between certain HLA-G polymorphisms and the mRNA levels of the different alternatively spliced HLA-G isoforms in first trimester trophoblast cell populations is reported. Several alternatively spliced HLA-G mRNA isoforms, including a 14-bp polymorphism in the 3'UTR end (exon 8) of the HLA-G gene, are expressed at a significantly lower level than the corresponding HLA-G mRNA isoforms with the 14-bp sequence deleted. Furthermore, characteristic HLA-G mRNA isoform expression patterns were associated with specific HLA-G genotypes and alleles. In the HLA-G*01012 and - G*01013 alleles that include the 14-bp sequence, an additional alternative splicing was observed, with the first 92-bp of exon 8 spliced out. This was most pronounced in HLA-G genotypes with G*01013. These findings may have functional implications for the recent reports of aberrant HLA-G expression and reproductive success. |
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Instead, HLA-G and -C, and possibly HLA-E, are expressed. HLA-G may modulate the immunological relationship between mother and fetus in several ways. Finally, the expression of membrane-bound HLA-G and soluble HLA-G has been proposed to influence the outcome of pregnancy, and an aberrant HLA-G expression in pre-eclamptic placentas and spontaneous abortions has been reported. Here, an association between certain HLA-G polymorphisms and the mRNA levels of the different alternatively spliced HLA-G isoforms in first trimester trophoblast cell populations is reported. Several alternatively spliced HLA-G mRNA isoforms, including a 14-bp polymorphism in the 3'UTR end (exon 8) of the HLA-G gene, are expressed at a significantly lower level than the corresponding HLA-G mRNA isoforms with the 14-bp sequence deleted. Furthermore, characteristic HLA-G mRNA isoform expression patterns were associated with specific HLA-G genotypes and alleles. In the HLA-G*01012 and - G*01013 alleles that include the 14-bp sequence, an additional alternative splicing was observed, with the first 92-bp of exon 8 spliced out. This was most pronounced in HLA-G genotypes with G*01013. These findings may have functional implications for the recent reports of aberrant HLA-G expression and reproductive success.</description><identifier>ISSN: 0093-7711</identifier><identifier>EISSN: 1432-1211</identifier><identifier>DOI: 10.1007/s00251-003-0547-z</identifier><identifier>PMID: 12712263</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Alternative Splicing ; Antigens ; Biochemistry ; Biopsy ; Cytokines ; Fetuses ; Gene Expression Profiling ; Genetic Variation ; Genotypes ; Histocompatibility Antigens Class I - genetics ; HLA Antigens - genetics ; HLA-G Antigens ; Humans ; Miscarriage ; Polymorphism ; Pregnancy ; Pregnancy complications ; Proteins ; Reproduction ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Trophoblasts - metabolism</subject><ispartof>Immunogenetics (New York), 2003-05, Vol.55 (2), p.63-79</ispartof><rights>Springer-Verlag 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-b2671e5c571d089bac55b542569becabfb9a41c348133ab04d3cf1c8d287a1923</citedby><cites>FETCH-LOGICAL-c355t-b2671e5c571d089bac55b542569becabfb9a41c348133ab04d3cf1c8d287a1923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12712263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hviid, Thomas Vauvert F</creatorcontrib><creatorcontrib>Hylenius, Sine</creatorcontrib><creatorcontrib>Rørbye, Christina</creatorcontrib><creatorcontrib>Nielsen, Lone G</creatorcontrib><title>HLA-G allelic variants are associated with differences in the HLA-G mRNA isoform profile and HLA-G mRNA levels</title><title>Immunogenetics (New York)</title><addtitle>Immunogenetics</addtitle><description>During pregnancy, the human extra-villous trophoblast in the contact zone between maternal and fetal tissue in the placenta does not express the classical MHC class I and II molecules. Instead, HLA-G and -C, and possibly HLA-E, are expressed. HLA-G may modulate the immunological relationship between mother and fetus in several ways. Finally, the expression of membrane-bound HLA-G and soluble HLA-G has been proposed to influence the outcome of pregnancy, and an aberrant HLA-G expression in pre-eclamptic placentas and spontaneous abortions has been reported. Here, an association between certain HLA-G polymorphisms and the mRNA levels of the different alternatively spliced HLA-G isoforms in first trimester trophoblast cell populations is reported. Several alternatively spliced HLA-G mRNA isoforms, including a 14-bp polymorphism in the 3'UTR end (exon 8) of the HLA-G gene, are expressed at a significantly lower level than the corresponding HLA-G mRNA isoforms with the 14-bp sequence deleted. Furthermore, characteristic HLA-G mRNA isoform expression patterns were associated with specific HLA-G genotypes and alleles. In the HLA-G*01012 and - G*01013 alleles that include the 14-bp sequence, an additional alternative splicing was observed, with the first 92-bp of exon 8 spliced out. This was most pronounced in HLA-G genotypes with G*01013. These findings may have functional implications for the recent reports of aberrant HLA-G expression and reproductive success.</description><subject>Alternative Splicing</subject><subject>Antigens</subject><subject>Biochemistry</subject><subject>Biopsy</subject><subject>Cytokines</subject><subject>Fetuses</subject><subject>Gene Expression Profiling</subject><subject>Genetic Variation</subject><subject>Genotypes</subject><subject>Histocompatibility Antigens Class I - genetics</subject><subject>HLA Antigens - genetics</subject><subject>HLA-G Antigens</subject><subject>Humans</subject><subject>Miscarriage</subject><subject>Polymorphism</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>Proteins</subject><subject>Reproduction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Trophoblasts - metabolism</subject><issn>0093-7711</issn><issn>1432-1211</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkU1LJDEQhoOs6OjuD9jLEvbgLVqVdDrdx0H8gkFB9BzS6WqMpLvdpEfRX28PM7DLXjzVod7npYqHsZ8IpwhgzjKA1CgAlABdGPGxxxZYKClQIn5jC4BaCWMQD9lRzs8AqGtZHrBDlAalLNWCDderpbjiLkaKwfNXl4IbpsxdIu5yHn1wE7X8LUxPvA1dR4kGT5mHgU9PxLd0f3-75CGP3Zh6_pLGLsSZHtp_15FeKebvbL9zMdOP3Txmj5cXD-fXYnV3dXO-XAmvtJ5EI0uDpL022EJVN85r3ehC6rJuyLuma2pXoFdFhUq5BopW-Q591crKOKylOmYn2975mj9rypPtQ_YUoxtoXGdrlEIwqL8MYmVMXZflHPz9X_B5XKdhfmJTBvMdetOG25BPY86JOvuSQu_Su0WwG2V2q8zOyuxGmf2YmV-74nXTU_uX2DlSn9WAjzk</recordid><startdate>200305</startdate><enddate>200305</enddate><creator>Hviid, Thomas Vauvert F</creator><creator>Hylenius, Sine</creator><creator>Rørbye, Christina</creator><creator>Nielsen, Lone G</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200305</creationdate><title>HLA-G allelic variants are associated with differences in the HLA-G mRNA isoform profile and HLA-G mRNA levels</title><author>Hviid, Thomas Vauvert F ; Hylenius, Sine ; Rørbye, Christina ; Nielsen, Lone G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-b2671e5c571d089bac55b542569becabfb9a41c348133ab04d3cf1c8d287a1923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alternative Splicing</topic><topic>Antigens</topic><topic>Biochemistry</topic><topic>Biopsy</topic><topic>Cytokines</topic><topic>Fetuses</topic><topic>Gene Expression Profiling</topic><topic>Genetic Variation</topic><topic>Genotypes</topic><topic>Histocompatibility Antigens Class I - genetics</topic><topic>HLA Antigens - genetics</topic><topic>HLA-G Antigens</topic><topic>Humans</topic><topic>Miscarriage</topic><topic>Polymorphism</topic><topic>Pregnancy</topic><topic>Pregnancy complications</topic><topic>Proteins</topic><topic>Reproduction</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Trophoblasts - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hviid, Thomas Vauvert F</creatorcontrib><creatorcontrib>Hylenius, Sine</creatorcontrib><creatorcontrib>Rørbye, Christina</creatorcontrib><creatorcontrib>Nielsen, Lone G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunogenetics (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hviid, Thomas Vauvert F</au><au>Hylenius, Sine</au><au>Rørbye, Christina</au><au>Nielsen, Lone G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA-G allelic variants are associated with differences in the HLA-G mRNA isoform profile and HLA-G mRNA levels</atitle><jtitle>Immunogenetics (New York)</jtitle><addtitle>Immunogenetics</addtitle><date>2003-05</date><risdate>2003</risdate><volume>55</volume><issue>2</issue><spage>63</spage><epage>79</epage><pages>63-79</pages><issn>0093-7711</issn><eissn>1432-1211</eissn><abstract>During pregnancy, the human extra-villous trophoblast in the contact zone between maternal and fetal tissue in the placenta does not express the classical MHC class I and II molecules. Instead, HLA-G and -C, and possibly HLA-E, are expressed. HLA-G may modulate the immunological relationship between mother and fetus in several ways. Finally, the expression of membrane-bound HLA-G and soluble HLA-G has been proposed to influence the outcome of pregnancy, and an aberrant HLA-G expression in pre-eclamptic placentas and spontaneous abortions has been reported. Here, an association between certain HLA-G polymorphisms and the mRNA levels of the different alternatively spliced HLA-G isoforms in first trimester trophoblast cell populations is reported. Several alternatively spliced HLA-G mRNA isoforms, including a 14-bp polymorphism in the 3'UTR end (exon 8) of the HLA-G gene, are expressed at a significantly lower level than the corresponding HLA-G mRNA isoforms with the 14-bp sequence deleted. Furthermore, characteristic HLA-G mRNA isoform expression patterns were associated with specific HLA-G genotypes and alleles. In the HLA-G*01012 and - G*01013 alleles that include the 14-bp sequence, an additional alternative splicing was observed, with the first 92-bp of exon 8 spliced out. This was most pronounced in HLA-G genotypes with G*01013. These findings may have functional implications for the recent reports of aberrant HLA-G expression and reproductive success.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>12712263</pmid><doi>10.1007/s00251-003-0547-z</doi><tpages>17</tpages></addata></record> |
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subjects | Alternative Splicing Antigens Biochemistry Biopsy Cytokines Fetuses Gene Expression Profiling Genetic Variation Genotypes Histocompatibility Antigens Class I - genetics HLA Antigens - genetics HLA-G Antigens Humans Miscarriage Polymorphism Pregnancy Pregnancy complications Proteins Reproduction Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics RNA, Messenger - metabolism Trophoblasts - metabolism |
title | HLA-G allelic variants are associated with differences in the HLA-G mRNA isoform profile and HLA-G mRNA levels |
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