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Autoimmunity-associated intronic SNP (rs2281808) detected by a simple phenotypic assay: Unique case or broader opportunity?
Multiple genome-wide association studies have shown that the single-nucleotide polymorphism (SNP) rs2281808 TT variant, present within the signal regulatory protein gamma (SIRPG) gene, is associated with autoimmune diseases, such as type 1 diabetes. SIRPγ is the only SIRP expressed on T cells. The r...
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Published in: | Clinical immunology (Orlando, Fla.) Fla.), 2019-01, Vol.198, p.57-61 |
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description | Multiple genome-wide association studies have shown that the single-nucleotide polymorphism (SNP) rs2281808 TT variant, present within the signal regulatory protein gamma (SIRPG) gene, is associated with autoimmune diseases, such as type 1 diabetes. SIRPγ is the only SIRP expressed on T cells. The role of SIRPγ in human T-cells or the effect of the TT variant are poorly understood. In this short report, we demonstrate the rather unusual finding that this intronic SNP is associated with a reduction of SIRPγ expression on T cells, both in healthy subjects as well as patients with type 1 diabetes. Using this information, we propose that a simple flow cytometric detection of SIRPγ could be a potential diagnostic testing approach for the presence of SNP in the appropriate clinical context.
•This is an interesting example of a phenotypic assay of protein expression tightly correlating with an intronic SNP.•A single-nucleotide polymorphism (SNP) in the SIRPG gene (rs2281808) is known to be associated with autoimmune disease.•SNP rs2281808 can be detected by a flow cytometric assay detecting the expression of the corresponding protein on T-cells.•The expression pattern may allow such detection to be utilized as a clinical diagnostic/prognostic test for rs2281808. |
doi_str_mv | 10.1016/j.clim.2018.12.018 |
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•This is an interesting example of a phenotypic assay of protein expression tightly correlating with an intronic SNP.•A single-nucleotide polymorphism (SNP) in the SIRPG gene (rs2281808) is known to be associated with autoimmune disease.•SNP rs2281808 can be detected by a flow cytometric assay detecting the expression of the corresponding protein on T-cells.•The expression pattern may allow such detection to be utilized as a clinical diagnostic/prognostic test for rs2281808.</description><identifier>ISSN: 1521-6616</identifier><identifier>EISSN: 1521-7035</identifier><identifier>DOI: 10.1016/j.clim.2018.12.018</identifier><identifier>PMID: 30579937</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antigens, Differentiation - genetics ; Autoimmunity ; Diabetes Mellitus, Type 1 - genetics ; Diagnostic ; Flow Cytometry ; Genotype ; Humans ; Middle Aged ; Phenotype ; Polymorphism, Single Nucleotide ; Receptors, Immunologic - genetics ; SIRPγ ; SNP rs2281808 ; Young Adult</subject><ispartof>Clinical immunology (Orlando, Fla.), 2019-01, Vol.198, p.57-61</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-283eb150be0a12d6950894cd385e431fc1c1e84553fe665c4853415fc3f208433</citedby><cites>FETCH-LOGICAL-c455t-283eb150be0a12d6950894cd385e431fc1c1e84553fe665c4853415fc3f208433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30579937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinha, Sushmita</creatorcontrib><creatorcontrib>Renavikar, Pranav S.</creatorcontrib><creatorcontrib>Crawford, Michael P.</creatorcontrib><creatorcontrib>Rodgers, Jake W.</creatorcontrib><creatorcontrib>Tsalikian, Eva</creatorcontrib><creatorcontrib>Tansey, Michael</creatorcontrib><creatorcontrib>Karandikar, Nitin J.</creatorcontrib><title>Autoimmunity-associated intronic SNP (rs2281808) detected by a simple phenotypic assay: Unique case or broader opportunity?</title><title>Clinical immunology (Orlando, Fla.)</title><addtitle>Clin Immunol</addtitle><description>Multiple genome-wide association studies have shown that the single-nucleotide polymorphism (SNP) rs2281808 TT variant, present within the signal regulatory protein gamma (SIRPG) gene, is associated with autoimmune diseases, such as type 1 diabetes. SIRPγ is the only SIRP expressed on T cells. The role of SIRPγ in human T-cells or the effect of the TT variant are poorly understood. In this short report, we demonstrate the rather unusual finding that this intronic SNP is associated with a reduction of SIRPγ expression on T cells, both in healthy subjects as well as patients with type 1 diabetes. Using this information, we propose that a simple flow cytometric detection of SIRPγ could be a potential diagnostic testing approach for the presence of SNP in the appropriate clinical context.
•This is an interesting example of a phenotypic assay of protein expression tightly correlating with an intronic SNP.•A single-nucleotide polymorphism (SNP) in the SIRPG gene (rs2281808) is known to be associated with autoimmune disease.•SNP rs2281808 can be detected by a flow cytometric assay detecting the expression of the corresponding protein on T-cells.•The expression pattern may allow such detection to be utilized as a clinical diagnostic/prognostic test for rs2281808.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antigens, Differentiation - genetics</subject><subject>Autoimmunity</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Diagnostic</subject><subject>Flow Cytometry</subject><subject>Genotype</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Phenotype</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Receptors, Immunologic - genetics</subject><subject>SIRPγ</subject><subject>SNP rs2281808</subject><subject>Young Adult</subject><issn>1521-6616</issn><issn>1521-7035</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kUtv1DAUhS0EomXgD7BAXpZFgq8dexyEQFVVHlIFSNC15Tg31KMkDnZSKeLP4-kMFWxYHUv-7rmPQ8hzYCUwUK92pev9UHIGugReZnlATkFyKLZMyIfHt1KgTsiTlHaMMcm5ekxOBJPbuhbbU_LrfJmDH4Zl9PNa2JSC83bGlvpxjmH0jn77_JWexcS5Bs30S9rijG5PNCu1NPlh6pFONziGeZ0ynz3s-ppej_7ngtTZhDRE2sRgW4w0TFOI8123d0_Jo872CZ8ddUOu319-v_hYXH358Oni_KpwlZRzwbXABiRrkFngraol03XlWqElVgI6Bw5QZ1R0qJR0lZaiAtk50XGmKyE25O3Bd1qaAVuHeTXbmyn6wcbVBOvNvz-jvzE_wq1RIt8uO2zI2dEghrxUms3gk8O-tyOGJRkOikGloaozyg-oiyGliN19G2Bmn5rZmX1qZp-aAW6y5KIXfw94X_Inpgy8OQCYz3TrMZrkPI4OWx9zGKYN_n_-vwHSjanq</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Sinha, Sushmita</creator><creator>Renavikar, Pranav S.</creator><creator>Crawford, Michael P.</creator><creator>Rodgers, Jake W.</creator><creator>Tsalikian, Eva</creator><creator>Tansey, Michael</creator><creator>Karandikar, Nitin J.</creator><general>Elsevier Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>Autoimmunity-associated intronic SNP (rs2281808) detected by a simple phenotypic assay: Unique case or broader opportunity?</title><author>Sinha, Sushmita ; Renavikar, Pranav S. ; Crawford, Michael P. ; Rodgers, Jake W. ; Tsalikian, Eva ; Tansey, Michael ; Karandikar, Nitin J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-283eb150be0a12d6950894cd385e431fc1c1e84553fe665c4853415fc3f208433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antigens, Differentiation - genetics</topic><topic>Autoimmunity</topic><topic>Diabetes Mellitus, Type 1 - genetics</topic><topic>Diagnostic</topic><topic>Flow Cytometry</topic><topic>Genotype</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Receptors, Immunologic - genetics</topic><topic>SIRPγ</topic><topic>SNP rs2281808</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sinha, Sushmita</creatorcontrib><creatorcontrib>Renavikar, Pranav S.</creatorcontrib><creatorcontrib>Crawford, Michael P.</creatorcontrib><creatorcontrib>Rodgers, Jake W.</creatorcontrib><creatorcontrib>Tsalikian, Eva</creatorcontrib><creatorcontrib>Tansey, Michael</creatorcontrib><creatorcontrib>Karandikar, Nitin J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical immunology (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sinha, Sushmita</au><au>Renavikar, Pranav S.</au><au>Crawford, Michael P.</au><au>Rodgers, Jake W.</au><au>Tsalikian, Eva</au><au>Tansey, Michael</au><au>Karandikar, Nitin J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autoimmunity-associated intronic SNP (rs2281808) detected by a simple phenotypic assay: Unique case or broader opportunity?</atitle><jtitle>Clinical immunology (Orlando, Fla.)</jtitle><addtitle>Clin Immunol</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>198</volume><spage>57</spage><epage>61</epage><pages>57-61</pages><issn>1521-6616</issn><eissn>1521-7035</eissn><abstract>Multiple genome-wide association studies have shown that the single-nucleotide polymorphism (SNP) rs2281808 TT variant, present within the signal regulatory protein gamma (SIRPG) gene, is associated with autoimmune diseases, such as type 1 diabetes. SIRPγ is the only SIRP expressed on T cells. The role of SIRPγ in human T-cells or the effect of the TT variant are poorly understood. In this short report, we demonstrate the rather unusual finding that this intronic SNP is associated with a reduction of SIRPγ expression on T cells, both in healthy subjects as well as patients with type 1 diabetes. Using this information, we propose that a simple flow cytometric detection of SIRPγ could be a potential diagnostic testing approach for the presence of SNP in the appropriate clinical context.
•This is an interesting example of a phenotypic assay of protein expression tightly correlating with an intronic SNP.•A single-nucleotide polymorphism (SNP) in the SIRPG gene (rs2281808) is known to be associated with autoimmune disease.•SNP rs2281808 can be detected by a flow cytometric assay detecting the expression of the corresponding protein on T-cells.•The expression pattern may allow such detection to be utilized as a clinical diagnostic/prognostic test for rs2281808.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30579937</pmid><doi>10.1016/j.clim.2018.12.018</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antigens, Differentiation - genetics Autoimmunity Diabetes Mellitus, Type 1 - genetics Diagnostic Flow Cytometry Genotype Humans Middle Aged Phenotype Polymorphism, Single Nucleotide Receptors, Immunologic - genetics SIRPγ SNP rs2281808 Young Adult |
title | Autoimmunity-associated intronic SNP (rs2281808) detected by a simple phenotypic assay: Unique case or broader opportunity? |
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