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Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population

:  Psoriasis is a chronic skin disease that results in red and scaly lesions. Several psoriasis susceptibility loci have been identified across the genome, of which PSORS1 on 6p21.3 is predominant. There is an ongoing debate regarding whether the HLA‐C allele, Cw*0602, can be considered the major pr...

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Published in:Experimental dermatology 2003-08, Vol.12 (4), p.435-444
Main Authors: Holm, Sofia J., Carlén, Lina M., Mallbris, Lotus, Ståhle-Bäckdahl, Mona, O'Brien, Kevin P.
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container_issue 4
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container_title Experimental dermatology
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creator Holm, Sofia J.
Carlén, Lina M.
Mallbris, Lotus
Ståhle-Bäckdahl, Mona
O'Brien, Kevin P.
description :  Psoriasis is a chronic skin disease that results in red and scaly lesions. Several psoriasis susceptibility loci have been identified across the genome, of which PSORS1 on 6p21.3 is predominant. There is an ongoing debate regarding whether the HLA‐C allele, Cw*0602, can be considered the major predisposing factor in this region. Investigation of other genes in the PSORS1 region with regard to psoriasis may provide alternate candidates to HLA‐C. We have characterized two overlapping genes, SEEK1 and SPR1. SEEK1 encodes two putative protein isoforms: the first being one of 152 amino acids from the full‐length splice‐isoform (exon 1–6), and the second being one of 100 amino acids from an alternate splice‐isoform (exon 1 and 6). SPR1 encodes a highly conserved protein of 134 amino acids, and in addition to characterization of human SPR1 we report the cloning of its orthologs in mouse and pig. Both SEEK1 and SPR1 are expressed in normal and psoriasis skin. In a case–control study, five of the nine single nucleotide polymorphisms (SNPs) found in SEEK1 were associated with psoriasis, while one of the four SNPs found in SPR1 showed association. Testing the Cw*0602 confounding status revealed that two of the SEEK1 SNPs showed Cw*0602‐independent association, while the SPR1 SNP showed Cw*0602‐dependent association. The second exon of SEEK1, containing the two Cw*0602‐independent SNPs, showed the highest concentration of the psoriasis‐associating SNPs, but did not appear to be translated.
doi_str_mv 10.1034/j.1600-0625.2003.00048.x
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Several psoriasis susceptibility loci have been identified across the genome, of which PSORS1 on 6p21.3 is predominant. There is an ongoing debate regarding whether the HLA‐C allele, Cw*0602, can be considered the major predisposing factor in this region. Investigation of other genes in the PSORS1 region with regard to psoriasis may provide alternate candidates to HLA‐C. We have characterized two overlapping genes, SEEK1 and SPR1. SEEK1 encodes two putative protein isoforms: the first being one of 152 amino acids from the full‐length splice‐isoform (exon 1–6), and the second being one of 100 amino acids from an alternate splice‐isoform (exon 1 and 6). SPR1 encodes a highly conserved protein of 134 amino acids, and in addition to characterization of human SPR1 we report the cloning of its orthologs in mouse and pig. Both SEEK1 and SPR1 are expressed in normal and psoriasis skin. In a case–control study, five of the nine single nucleotide polymorphisms (SNPs) found in SEEK1 were associated with psoriasis, while one of the four SNPs found in SPR1 showed association. Testing the Cw*0602 confounding status revealed that two of the SEEK1 SNPs showed Cw*0602‐independent association, while the SPR1 SNP showed Cw*0602‐dependent association. The second exon of SEEK1, containing the two Cw*0602‐independent SNPs, showed the highest concentration of the psoriasis‐associating SNPs, but did not appear to be translated.</description><identifier>ISSN: 0906-6705</identifier><identifier>EISSN: 1600-0625</identifier><identifier>DOI: 10.1034/j.1600-0625.2003.00048.x</identifier><identifier>PMID: 12930300</identifier><language>eng</language><publisher>Oxford, UK: Munksgaard International Publishers</publisher><subject>Adolescent ; Adult ; Aged ; Amino Acid Sequence ; Animals ; Base Sequence ; Biological and medical sciences ; Case-Control Studies ; Child ; Child, Preschool ; Chromosome Mapping ; Chromosomes, Human, Pair 6 - genetics ; Cloning, Molecular ; Cornified Envelope Proline-Rich Proteins ; Dermatology ; DNA, Complementary - genetics ; Female ; Gene Expression ; genetic disease ; HLA-C ; HLA-C Antigens - genetics ; Humans ; Infant ; major histocompatibility complex ; Male ; Medical sciences ; Medicin och hälsovetenskap ; Membrane Proteins ; Mice ; Middle Aged ; Molecular Sequence Data ; Polymorphism, Single Nucleotide ; Protein Isoforms - genetics ; Proteins - genetics ; psoriasis ; Psoriasis - genetics ; Psoriasis. 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Several psoriasis susceptibility loci have been identified across the genome, of which PSORS1 on 6p21.3 is predominant. There is an ongoing debate regarding whether the HLA‐C allele, Cw*0602, can be considered the major predisposing factor in this region. Investigation of other genes in the PSORS1 region with regard to psoriasis may provide alternate candidates to HLA‐C. We have characterized two overlapping genes, SEEK1 and SPR1. SEEK1 encodes two putative protein isoforms: the first being one of 152 amino acids from the full‐length splice‐isoform (exon 1–6), and the second being one of 100 amino acids from an alternate splice‐isoform (exon 1 and 6). SPR1 encodes a highly conserved protein of 134 amino acids, and in addition to characterization of human SPR1 we report the cloning of its orthologs in mouse and pig. Both SEEK1 and SPR1 are expressed in normal and psoriasis skin. In a case–control study, five of the nine single nucleotide polymorphisms (SNPs) found in SEEK1 were associated with psoriasis, while one of the four SNPs found in SPR1 showed association. Testing the Cw*0602 confounding status revealed that two of the SEEK1 SNPs showed Cw*0602‐independent association, while the SPR1 SNP showed Cw*0602‐dependent association. The second exon of SEEK1, containing the two Cw*0602‐independent SNPs, showed the highest concentration of the psoriasis‐associating SNPs, but did not appear to be translated.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 6 - genetics</subject><subject>Cloning, Molecular</subject><subject>Cornified Envelope Proline-Rich Proteins</subject><subject>Dermatology</subject><subject>DNA, Complementary - genetics</subject><subject>Female</subject><subject>Gene Expression</subject><subject>genetic disease</subject><subject>HLA-C</subject><subject>HLA-C Antigens - genetics</subject><subject>Humans</subject><subject>Infant</subject><subject>major histocompatibility complex</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicin och hälsovetenskap</subject><subject>Membrane Proteins</subject><subject>Mice</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Protein Isoforms - genetics</subject><subject>Proteins - genetics</subject><subject>psoriasis</subject><subject>Psoriasis - genetics</subject><subject>Psoriasis. 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Lichen</subject><subject>Sequence Homology, Amino Acid</subject><subject>Sus scrofa</subject><subject>Sweden</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNks1u1DAURiMEokPhFZA3sEt6r3-SWGKD2mEoraCiBbqz3MRhPE3iECeambcnYcJkhcTKV_Y5tq8_BwFBiBAYP9tEGAOEEFMRUQAWAQBPo92TYHFceBosQEIcxgmIk-CF9xsATFgingcnSCUDBrAIihtX7ivXNmvrK09sTbq1IbfL5RUSXefk9uYrkp-mNp64msQNxYgR7b3LrO4M2dpuTRrvWqu9nfWtya0fFlzTl7qzrn4ZPCt06c2raTwNvn1Y3p1_DK-_rC7P31-HmcA0DfMU0YAQEoucpUxkOTLGuYaEcUMlpzFLM4kJZXxsm2oGyGWuZU4zRIrsNAgP-_qtafoH1bS20u1eOW3VNPU4VEaJNE2AD3zyT75pXT5Lf0WUHDEZzbcHc8B-9cZ3qrI-M2Wpa-N6rxIWi5iCHMD0AGat8741xfEQBDWmqTZqDE2NoamxLfUnTbUb1NfTGf1DZfJZnOIbgDcToH2my6LVdWb9zHHJU4li4N4duK0tzf6_L6CW9xdDMb-q9Z3ZHXXdPqp4_FHqx-eVur_7_mkVXzEl2G_w98fH</recordid><startdate>200308</startdate><enddate>200308</enddate><creator>Holm, Sofia J.</creator><creator>Carlén, Lina M.</creator><creator>Mallbris, Lotus</creator><creator>Ståhle-Bäckdahl, Mona</creator><creator>O'Brien, Kevin P.</creator><general>Munksgaard International Publishers</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><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>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>200308</creationdate><title>Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population</title><author>Holm, Sofia J. ; Carlén, Lina M. ; Mallbris, Lotus ; Ståhle-Bäckdahl, Mona ; O'Brien, Kevin P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5188-d811e05591fd3835cd13344a0734e2942638c91723420032a30149da9d2c11213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Pair 6 - genetics</topic><topic>Cloning, Molecular</topic><topic>Cornified Envelope Proline-Rich Proteins</topic><topic>Dermatology</topic><topic>DNA, Complementary - genetics</topic><topic>Female</topic><topic>Gene Expression</topic><topic>genetic disease</topic><topic>HLA-C</topic><topic>HLA-C Antigens - genetics</topic><topic>Humans</topic><topic>Infant</topic><topic>major histocompatibility complex</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicin och hälsovetenskap</topic><topic>Membrane Proteins</topic><topic>Mice</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Protein Isoforms - genetics</topic><topic>Proteins - genetics</topic><topic>psoriasis</topic><topic>Psoriasis - genetics</topic><topic>Psoriasis. Parapsoriasis. Lichen</topic><topic>Sequence Homology, Amino Acid</topic><topic>Sus scrofa</topic><topic>Sweden</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holm, Sofia J.</creatorcontrib><creatorcontrib>Carlén, Lina M.</creatorcontrib><creatorcontrib>Mallbris, Lotus</creatorcontrib><creatorcontrib>Ståhle-Bäckdahl, Mona</creatorcontrib><creatorcontrib>O'Brien, Kevin P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>SwePub</collection><collection>SwePub Articles</collection><jtitle>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holm, Sofia J.</au><au>Carlén, Lina M.</au><au>Mallbris, Lotus</au><au>Ståhle-Bäckdahl, Mona</au><au>O'Brien, Kevin P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2003-08</date><risdate>2003</risdate><volume>12</volume><issue>4</issue><spage>435</spage><epage>444</epage><pages>435-444</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>:  Psoriasis is a chronic skin disease that results in red and scaly lesions. Several psoriasis susceptibility loci have been identified across the genome, of which PSORS1 on 6p21.3 is predominant. There is an ongoing debate regarding whether the HLA‐C allele, Cw*0602, can be considered the major predisposing factor in this region. Investigation of other genes in the PSORS1 region with regard to psoriasis may provide alternate candidates to HLA‐C. We have characterized two overlapping genes, SEEK1 and SPR1. SEEK1 encodes two putative protein isoforms: the first being one of 152 amino acids from the full‐length splice‐isoform (exon 1–6), and the second being one of 100 amino acids from an alternate splice‐isoform (exon 1 and 6). SPR1 encodes a highly conserved protein of 134 amino acids, and in addition to characterization of human SPR1 we report the cloning of its orthologs in mouse and pig. Both SEEK1 and SPR1 are expressed in normal and psoriasis skin. In a case–control study, five of the nine single nucleotide polymorphisms (SNPs) found in SEEK1 were associated with psoriasis, while one of the four SNPs found in SPR1 showed association. Testing the Cw*0602 confounding status revealed that two of the SEEK1 SNPs showed Cw*0602‐independent association, while the SPR1 SNP showed Cw*0602‐dependent association. The second exon of SEEK1, containing the two Cw*0602‐independent SNPs, showed the highest concentration of the psoriasis‐associating SNPs, but did not appear to be translated.</abstract><cop>Oxford, UK</cop><pub>Munksgaard International Publishers</pub><pmid>12930300</pmid><doi>10.1034/j.1600-0625.2003.00048.x</doi><tpages>10</tpages></addata></record>
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identifier ISSN: 0906-6705
ispartof Experimental dermatology, 2003-08, Vol.12 (4), p.435-444
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1600-0625
language eng
recordid cdi_swepub_primary_oai_swepub_ki_se_588704
source Wiley
subjects Adolescent
Adult
Aged
Amino Acid Sequence
Animals
Base Sequence
Biological and medical sciences
Case-Control Studies
Child
Child, Preschool
Chromosome Mapping
Chromosomes, Human, Pair 6 - genetics
Cloning, Molecular
Cornified Envelope Proline-Rich Proteins
Dermatology
DNA, Complementary - genetics
Female
Gene Expression
genetic disease
HLA-C
HLA-C Antigens - genetics
Humans
Infant
major histocompatibility complex
Male
Medical sciences
Medicin och hälsovetenskap
Membrane Proteins
Mice
Middle Aged
Molecular Sequence Data
Polymorphism, Single Nucleotide
Protein Isoforms - genetics
Proteins - genetics
psoriasis
Psoriasis - genetics
Psoriasis. Parapsoriasis. Lichen
Sequence Homology, Amino Acid
Sus scrofa
Sweden
title Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population
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