A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms
Background and Objectives An Australian Caucasian blood donor consistently presented a serology profile for the Duffy blood group as Fy(a+b+) with Fya antigen expression weaker than other examples of Fy(a+b+) red cells. Molecular typing studies were performed to investigate the reason for the observ...
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Veröffentlicht in: | Vox sanguinis 2015-01, Vol.108 (1), p.52-57 |
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creator | Lopez, G. H. Condon, J. A. Wilson, B. Martin, J. R. Liew, Y.-W. Flower, R. L. Hyland, C. A. |
description | Background and Objectives
An Australian Caucasian blood donor consistently presented a serology profile for the Duffy blood group as Fy(a+b+) with Fya antigen expression weaker than other examples of Fy(a+b+) red cells. Molecular typing studies were performed to investigate the reason for the observed serology profile.
Material and Methods
Blood group genotyping was performed using a commercial SNP microarray platform. Sanger sequencing was performed using primer sets to amplify across exons 1 and 2 of the FY gene and using allele‐specific primers.
Results
The propositus was genotyped as FY*A/B, FY*X heterozygote that predicted the Fy(a+b+w) phenotype. Sequencing identified the 265T and 298A variants on the FY*A allele. This link between FY*A allele and 265T was confirmed by allele‐specific PCR.
Conclusion
The reduced Fya antigen reactivity is attributed to a FY*A allele‐carrying 265T and 298A variants previously defined in combination only with the FY*B allele and associated with weak Fyb antigen expression. This novel allele should be considered in genotyping interpretative algorithms for generating a predicted phenotype. |
doi_str_mv | 10.1111/vox.12185 |
format | Article |
fullrecord | <record><control><sourceid>proquest_wiley</sourceid><recordid>TN_cdi_proquest_journals_1638717859</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3532670371</sourcerecordid><originalsourceid>FETCH-LOGICAL-i1065-127ad3c6e0daf1535a342d5676a2ed1a57be3fdc6696ee5d6b546f8b4a34bac33</originalsourceid><addsrcrecordid>eNpFkUtvEzEUhS0EEqGw4B9YYj2tH2N7wi4U0iKiFkF4lI3lmbmTunXGg-085p_x83AaHt5cX91zvrM4CL2k5JTmd7b1-1PKaCUeoQktGS9IScljNCGkZMWUEPUUPYvxjhBSsUpM0K8Z7v0WHJ7fzLBxDhzgnU23ON0CZlIsselbzKbVDH---hhx58MaghuxidE31iRoMewbt4k2U8b_3vnNm7-8A2EH5h7Pxzovya6gz6YhQIzW96-xXQ_ONibl5RCA892ncbD9Cts-QcjKlK_bjHIrH3LEOj5HTzrjIrz4M0_Ql_m75fllsbi-eH8-WxSWEikKypRpeSOBtKajggvDS9YKqaRh0FIjVA28axsppxJAtLIWpeyqusy62jScn6BXR-4Q_M8NxKTv_Cb0OVJTyStFVSWmWXV2VO2sg1EPwa5NGDUl-tCKzq3oh1b01-vvD5_sKI4OGxPs_zlMuNdScSX0t6sL_eHH28WSqE_6kv8GPY-T9w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1638717859</pqid></control><display><type>article</type><title>A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms</title><source>Access via Wiley Online Library</source><creator>Lopez, G. H. ; Condon, J. A. ; Wilson, B. ; Martin, J. R. ; Liew, Y.-W. ; Flower, R. L. ; Hyland, C. A.</creator><creatorcontrib>Lopez, G. H. ; Condon, J. A. ; Wilson, B. ; Martin, J. R. ; Liew, Y.-W. ; Flower, R. L. ; Hyland, C. A.</creatorcontrib><description>Background and Objectives
An Australian Caucasian blood donor consistently presented a serology profile for the Duffy blood group as Fy(a+b+) with Fya antigen expression weaker than other examples of Fy(a+b+) red cells. Molecular typing studies were performed to investigate the reason for the observed serology profile.
Material and Methods
Blood group genotyping was performed using a commercial SNP microarray platform. Sanger sequencing was performed using primer sets to amplify across exons 1 and 2 of the FY gene and using allele‐specific primers.
Results
The propositus was genotyped as FY*A/B, FY*X heterozygote that predicted the Fy(a+b+w) phenotype. Sequencing identified the 265T and 298A variants on the FY*A allele. This link between FY*A allele and 265T was confirmed by allele‐specific PCR.
Conclusion
The reduced Fya antigen reactivity is attributed to a FY*A allele‐carrying 265T and 298A variants previously defined in combination only with the FY*B allele and associated with weak Fyb antigen expression. This novel allele should be considered in genotyping interpretative algorithms for generating a predicted phenotype.</description><identifier>ISSN: 0042-9007</identifier><identifier>EISSN: 1423-0410</identifier><identifier>DOI: 10.1111/vox.12185</identifier><identifier>CODEN: VOSAAD</identifier><language>eng</language><publisher>Amsterdam: Blackwell Publishing Ltd</publisher><subject>Algorithms ; Antigens ; Blood & organ donations ; Duffy blood group ; FY01W.02 ; Genes ; Hematology ; novel FYA allele ; reduced Fya expression</subject><ispartof>Vox sanguinis, 2015-01, Vol.108 (1), p.52-57</ispartof><rights>2014 International Society of Blood Transfusion</rights><rights>Copyright Vox Sanguinis © 2015 International Society of Blood Transfusion</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fvox.12185$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fvox.12185$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Lopez, G. H.</creatorcontrib><creatorcontrib>Condon, J. A.</creatorcontrib><creatorcontrib>Wilson, B.</creatorcontrib><creatorcontrib>Martin, J. R.</creatorcontrib><creatorcontrib>Liew, Y.-W.</creatorcontrib><creatorcontrib>Flower, R. L.</creatorcontrib><creatorcontrib>Hyland, C. A.</creatorcontrib><title>A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms</title><title>Vox sanguinis</title><addtitle>Vox Sang</addtitle><description>Background and Objectives
An Australian Caucasian blood donor consistently presented a serology profile for the Duffy blood group as Fy(a+b+) with Fya antigen expression weaker than other examples of Fy(a+b+) red cells. Molecular typing studies were performed to investigate the reason for the observed serology profile.
Material and Methods
Blood group genotyping was performed using a commercial SNP microarray platform. Sanger sequencing was performed using primer sets to amplify across exons 1 and 2 of the FY gene and using allele‐specific primers.
Results
The propositus was genotyped as FY*A/B, FY*X heterozygote that predicted the Fy(a+b+w) phenotype. Sequencing identified the 265T and 298A variants on the FY*A allele. This link between FY*A allele and 265T was confirmed by allele‐specific PCR.
Conclusion
The reduced Fya antigen reactivity is attributed to a FY*A allele‐carrying 265T and 298A variants previously defined in combination only with the FY*B allele and associated with weak Fyb antigen expression. This novel allele should be considered in genotyping interpretative algorithms for generating a predicted phenotype.</description><subject>Algorithms</subject><subject>Antigens</subject><subject>Blood & organ donations</subject><subject>Duffy blood group</subject><subject>FY01W.02</subject><subject>Genes</subject><subject>Hematology</subject><subject>novel FYA allele</subject><subject>reduced Fya expression</subject><issn>0042-9007</issn><issn>1423-0410</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpFkUtvEzEUhS0EEqGw4B9YYj2tH2N7wi4U0iKiFkF4lI3lmbmTunXGg-085p_x83AaHt5cX91zvrM4CL2k5JTmd7b1-1PKaCUeoQktGS9IScljNCGkZMWUEPUUPYvxjhBSsUpM0K8Z7v0WHJ7fzLBxDhzgnU23ON0CZlIsselbzKbVDH---hhx58MaghuxidE31iRoMewbt4k2U8b_3vnNm7-8A2EH5h7Pxzovya6gz6YhQIzW96-xXQ_ONibl5RCA892ncbD9Cts-QcjKlK_bjHIrH3LEOj5HTzrjIrz4M0_Ql_m75fllsbi-eH8-WxSWEikKypRpeSOBtKajggvDS9YKqaRh0FIjVA28axsppxJAtLIWpeyqusy62jScn6BXR-4Q_M8NxKTv_Cb0OVJTyStFVSWmWXV2VO2sg1EPwa5NGDUl-tCKzq3oh1b01-vvD5_sKI4OGxPs_zlMuNdScSX0t6sL_eHH28WSqE_6kv8GPY-T9w</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Lopez, G. H.</creator><creator>Condon, J. A.</creator><creator>Wilson, B.</creator><creator>Martin, J. R.</creator><creator>Liew, Y.-W.</creator><creator>Flower, R. L.</creator><creator>Hyland, C. A.</creator><general>Blackwell Publishing Ltd</general><general>S. Karger AG</general><scope>BSCLL</scope><scope>7QL</scope><scope>7T5</scope><scope>7TM</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope></search><sort><creationdate>201501</creationdate><title>A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms</title><author>Lopez, G. H. ; Condon, J. A. ; Wilson, B. ; Martin, J. R. ; Liew, Y.-W. ; Flower, R. L. ; Hyland, C. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i1065-127ad3c6e0daf1535a342d5676a2ed1a57be3fdc6696ee5d6b546f8b4a34bac33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Algorithms</topic><topic>Antigens</topic><topic>Blood & organ donations</topic><topic>Duffy blood group</topic><topic>FY01W.02</topic><topic>Genes</topic><topic>Hematology</topic><topic>novel FYA allele</topic><topic>reduced Fya expression</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lopez, G. H.</creatorcontrib><creatorcontrib>Condon, J. A.</creatorcontrib><creatorcontrib>Wilson, B.</creatorcontrib><creatorcontrib>Martin, J. R.</creatorcontrib><creatorcontrib>Liew, Y.-W.</creatorcontrib><creatorcontrib>Flower, R. L.</creatorcontrib><creatorcontrib>Hyland, C. A.</creatorcontrib><collection>Istex</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Vox sanguinis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lopez, G. H.</au><au>Condon, J. A.</au><au>Wilson, B.</au><au>Martin, J. R.</au><au>Liew, Y.-W.</au><au>Flower, R. L.</au><au>Hyland, C. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms</atitle><jtitle>Vox sanguinis</jtitle><addtitle>Vox Sang</addtitle><date>2015-01</date><risdate>2015</risdate><volume>108</volume><issue>1</issue><spage>52</spage><epage>57</epage><pages>52-57</pages><issn>0042-9007</issn><eissn>1423-0410</eissn><coden>VOSAAD</coden><abstract>Background and Objectives
An Australian Caucasian blood donor consistently presented a serology profile for the Duffy blood group as Fy(a+b+) with Fya antigen expression weaker than other examples of Fy(a+b+) red cells. Molecular typing studies were performed to investigate the reason for the observed serology profile.
Material and Methods
Blood group genotyping was performed using a commercial SNP microarray platform. Sanger sequencing was performed using primer sets to amplify across exons 1 and 2 of the FY gene and using allele‐specific primers.
Results
The propositus was genotyped as FY*A/B, FY*X heterozygote that predicted the Fy(a+b+w) phenotype. Sequencing identified the 265T and 298A variants on the FY*A allele. This link between FY*A allele and 265T was confirmed by allele‐specific PCR.
Conclusion
The reduced Fya antigen reactivity is attributed to a FY*A allele‐carrying 265T and 298A variants previously defined in combination only with the FY*B allele and associated with weak Fyb antigen expression. This novel allele should be considered in genotyping interpretative algorithms for generating a predicted phenotype.</abstract><cop>Amsterdam</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/vox.12185</doi><tpages>6</tpages></addata></record> |
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subjects | Algorithms Antigens Blood & organ donations Duffy blood group FY01W.02 Genes Hematology novel FYA allele reduced Fya expression |
title | A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms |
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