The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity
The dual-specificity phosphatase 6 (DUSP6) gene resides at chromosome location 12q22–23, which is one of the candidate loci for susceptibility to bipolar disorder and which encodes a phosphatase selective for extracellular signal-regulated kinase (ERK). Previously, we reported a positive association...
Gespeichert in:
Veröffentlicht in: | Progress in neuro-psychopharmacology & biological psychiatry 2012-04, Vol.37 (1), p.41-49 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 49 |
---|---|
container_issue | 1 |
container_start_page | 41 |
container_title | Progress in neuro-psychopharmacology & biological psychiatry |
container_volume | 37 |
creator | Kim, Se Hyun Shin, Soon Young Lee, Kyu Young Joo, Eun Jeong Song, Joo Youn Ahn, Yong Min Lee, Young Han Kim, Yong Sik |
description | The dual-specificity phosphatase 6 (DUSP6) gene resides at chromosome location 12q22–23, which is one of the candidate loci for susceptibility to bipolar disorder and which encodes a phosphatase selective for extracellular signal-regulated kinase (ERK). Previously, we reported a positive association between the functional Leu114Val polymorphism (rs2279574) in DUSP6 and bipolar disorder. Given that the association between DUSP6 and the reported down-regulation of DUSP6 transcript in bipolar postmortem brains were sex-dimorphic, showing significance in women but not men, we performed two independent analyses in homogenous samples of male and female Korean patients with bipolar disorder or schizophrenia using samples enlarged from our previous report. Among the examined DUSP6 SNPs, five (rs769700, rs704076, rs770087, rs808820, and rs2279574) showed positive allelic associations, with the frequency of minor alleles (C, T, G, G, and G) in each SNP significantly increased in women with BD. Consequently, the “C-T-G-G-G” haplotype was significantly over-represented (P=0.016; OR=3.242), whereas the “T-G-T-A-T” haplotype was significantly under-represented (P=0.014; OR=0.697). We found no significant associations with DUSP6 SNPs in men with bipolar disorder or schizophrenia. We also investigated the functions of the functional SNPs' positive associations and found that Leu114Val (rs2279574; T/G) and Ser144Ala (rs770087; T/G) mutations in DUSP6 proteins reduced lithium-induced ERK1/2 phosphorylation in vitro, implicating the dominant active functions. Thus, DUSP6 may not only play important roles in the pathogenesis of bipolar disorder, particularly in women, but also affect the therapeutic response to lithium through modulating lithium's effects on intracellular signaling.
► DUSP6 gene is shown to be associated with BD in Korea. ► Association between DUSP6 and BD is found in female patients. ► Leu114Val or Ser144Ala mutation of DUSP6 blunts the ERK activation by lithium. |
doi_str_mv | 10.1016/j.pnpbp.2011.11.014 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_926503762</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0278584611003447</els_id><sourcerecordid>1011210035</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-3d455fdcb0c90fa0f3cc5d9487375e6d379c1076a928ba55591c26829418282d3</originalsourceid><addsrcrecordid>eNp9kMFOGzEQhi1UVFLoEyBVvrWXpB577V0fOFRAW1QkEJCz5bVni6NkvbUdKt6-pgGOSL80c_j-Gekj5BjYAhior6vFNE79tOAMYFHDoNkjM-jabt5wUO_IjPG6y65RB-RDzivGGAgm3pMDzkFK0HxGlnf3SH_jiCU4anOOLtgS4kjjQM-Wt9eK_g3lnvZhimubqA85Jo-J2tHTUDLFYUBXaC2c3_yi1pXwEMrjEdkf7Drjx-d5SJbfz-9Of84vr35cnH67nDuhocyFb6QcvOuZ02ywbBDOSa-brhWtROVFqx2wVlnNu95KKTU4rjquG-h4x704JJ93d6cU_2wxF7MJ2eF6bUeM22w0V5KJVvFKfnmTrEaBA2NCVlTsUJdizgkHM6WwsemxQk-cMivz37x5Mm9qqvna-vT8YNtv0L92XlRX4GQHYBXyEDCZ7AKODn1IVaHxMbz54B-lgJNa</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1011210035</pqid></control><display><type>article</type><title>The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Kim, Se Hyun ; Shin, Soon Young ; Lee, Kyu Young ; Joo, Eun Jeong ; Song, Joo Youn ; Ahn, Yong Min ; Lee, Young Han ; Kim, Yong Sik</creator><creatorcontrib>Kim, Se Hyun ; Shin, Soon Young ; Lee, Kyu Young ; Joo, Eun Jeong ; Song, Joo Youn ; Ahn, Yong Min ; Lee, Young Han ; Kim, Yong Sik</creatorcontrib><description>The dual-specificity phosphatase 6 (DUSP6) gene resides at chromosome location 12q22–23, which is one of the candidate loci for susceptibility to bipolar disorder and which encodes a phosphatase selective for extracellular signal-regulated kinase (ERK). Previously, we reported a positive association between the functional Leu114Val polymorphism (rs2279574) in DUSP6 and bipolar disorder. Given that the association between DUSP6 and the reported down-regulation of DUSP6 transcript in bipolar postmortem brains were sex-dimorphic, showing significance in women but not men, we performed two independent analyses in homogenous samples of male and female Korean patients with bipolar disorder or schizophrenia using samples enlarged from our previous report. Among the examined DUSP6 SNPs, five (rs769700, rs704076, rs770087, rs808820, and rs2279574) showed positive allelic associations, with the frequency of minor alleles (C, T, G, G, and G) in each SNP significantly increased in women with BD. Consequently, the “C-T-G-G-G” haplotype was significantly over-represented (P=0.016; OR=3.242), whereas the “T-G-T-A-T” haplotype was significantly under-represented (P=0.014; OR=0.697). We found no significant associations with DUSP6 SNPs in men with bipolar disorder or schizophrenia. We also investigated the functions of the functional SNPs' positive associations and found that Leu114Val (rs2279574; T/G) and Ser144Ala (rs770087; T/G) mutations in DUSP6 proteins reduced lithium-induced ERK1/2 phosphorylation in vitro, implicating the dominant active functions. Thus, DUSP6 may not only play important roles in the pathogenesis of bipolar disorder, particularly in women, but also affect the therapeutic response to lithium through modulating lithium's effects on intracellular signaling.
► DUSP6 gene is shown to be associated with BD in Korea. ► Association between DUSP6 and BD is found in female patients. ► Leu114Val or Ser144Ala mutation of DUSP6 blunts the ERK activation by lithium.</description><identifier>ISSN: 0278-5846</identifier><identifier>EISSN: 1878-4216</identifier><identifier>DOI: 10.1016/j.pnpbp.2011.11.014</identifier><identifier>PMID: 22155192</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Adult ; Alleles ; Bipolar disorder ; Bipolar Disorder - enzymology ; Bipolar Disorder - genetics ; Brain ; Dual Specificity Phosphatase 6 - genetics ; Dual-specificity phosphatase 6 ; Enzyme Activation - genetics ; Enzyme Activation - physiology ; Extracellular signal-regulated kinase ; Female ; Gene frequency ; Genetic association ; Genetic Association Studies - methods ; Haplotypes ; HeLa Cells ; Humans ; Intracellular signalling ; Leu114Val polymorphism ; Lithium ; Male ; MAP Kinase Signaling System - genetics ; MAP Kinase Signaling System - physiology ; Mental disorders ; Middle Aged ; Mutation ; Phosphorylation ; Polymorphism, Single Nucleotide - genetics ; Schizophrenia ; Ser144Ala polymorphism ; Single-nucleotide polymorphism ; Transcription ; Young Adult</subject><ispartof>Progress in neuro-psychopharmacology & biological psychiatry, 2012-04, Vol.37 (1), p.41-49</ispartof><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-3d455fdcb0c90fa0f3cc5d9487375e6d379c1076a928ba55591c26829418282d3</citedby><cites>FETCH-LOGICAL-c391t-3d455fdcb0c90fa0f3cc5d9487375e6d379c1076a928ba55591c26829418282d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.pnpbp.2011.11.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22155192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Se Hyun</creatorcontrib><creatorcontrib>Shin, Soon Young</creatorcontrib><creatorcontrib>Lee, Kyu Young</creatorcontrib><creatorcontrib>Joo, Eun Jeong</creatorcontrib><creatorcontrib>Song, Joo Youn</creatorcontrib><creatorcontrib>Ahn, Yong Min</creatorcontrib><creatorcontrib>Lee, Young Han</creatorcontrib><creatorcontrib>Kim, Yong Sik</creatorcontrib><title>The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity</title><title>Progress in neuro-psychopharmacology & biological psychiatry</title><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><description>The dual-specificity phosphatase 6 (DUSP6) gene resides at chromosome location 12q22–23, which is one of the candidate loci for susceptibility to bipolar disorder and which encodes a phosphatase selective for extracellular signal-regulated kinase (ERK). Previously, we reported a positive association between the functional Leu114Val polymorphism (rs2279574) in DUSP6 and bipolar disorder. Given that the association between DUSP6 and the reported down-regulation of DUSP6 transcript in bipolar postmortem brains were sex-dimorphic, showing significance in women but not men, we performed two independent analyses in homogenous samples of male and female Korean patients with bipolar disorder or schizophrenia using samples enlarged from our previous report. Among the examined DUSP6 SNPs, five (rs769700, rs704076, rs770087, rs808820, and rs2279574) showed positive allelic associations, with the frequency of minor alleles (C, T, G, G, and G) in each SNP significantly increased in women with BD. Consequently, the “C-T-G-G-G” haplotype was significantly over-represented (P=0.016; OR=3.242), whereas the “T-G-T-A-T” haplotype was significantly under-represented (P=0.014; OR=0.697). We found no significant associations with DUSP6 SNPs in men with bipolar disorder or schizophrenia. We also investigated the functions of the functional SNPs' positive associations and found that Leu114Val (rs2279574; T/G) and Ser144Ala (rs770087; T/G) mutations in DUSP6 proteins reduced lithium-induced ERK1/2 phosphorylation in vitro, implicating the dominant active functions. Thus, DUSP6 may not only play important roles in the pathogenesis of bipolar disorder, particularly in women, but also affect the therapeutic response to lithium through modulating lithium's effects on intracellular signaling.
► DUSP6 gene is shown to be associated with BD in Korea. ► Association between DUSP6 and BD is found in female patients. ► Leu114Val or Ser144Ala mutation of DUSP6 blunts the ERK activation by lithium.</description><subject>Adult</subject><subject>Alleles</subject><subject>Bipolar disorder</subject><subject>Bipolar Disorder - enzymology</subject><subject>Bipolar Disorder - genetics</subject><subject>Brain</subject><subject>Dual Specificity Phosphatase 6 - genetics</subject><subject>Dual-specificity phosphatase 6</subject><subject>Enzyme Activation - genetics</subject><subject>Enzyme Activation - physiology</subject><subject>Extracellular signal-regulated kinase</subject><subject>Female</subject><subject>Gene frequency</subject><subject>Genetic association</subject><subject>Genetic Association Studies - methods</subject><subject>Haplotypes</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Intracellular signalling</subject><subject>Leu114Val polymorphism</subject><subject>Lithium</subject><subject>Male</subject><subject>MAP Kinase Signaling System - genetics</subject><subject>MAP Kinase Signaling System - physiology</subject><subject>Mental disorders</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Phosphorylation</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Schizophrenia</subject><subject>Ser144Ala polymorphism</subject><subject>Single-nucleotide polymorphism</subject><subject>Transcription</subject><subject>Young Adult</subject><issn>0278-5846</issn><issn>1878-4216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFOGzEQhi1UVFLoEyBVvrWXpB577V0fOFRAW1QkEJCz5bVni6NkvbUdKt6-pgGOSL80c_j-Gekj5BjYAhior6vFNE79tOAMYFHDoNkjM-jabt5wUO_IjPG6y65RB-RDzivGGAgm3pMDzkFK0HxGlnf3SH_jiCU4anOOLtgS4kjjQM-Wt9eK_g3lnvZhimubqA85Jo-J2tHTUDLFYUBXaC2c3_yi1pXwEMrjEdkf7Drjx-d5SJbfz-9Of84vr35cnH67nDuhocyFb6QcvOuZ02ywbBDOSa-brhWtROVFqx2wVlnNu95KKTU4rjquG-h4x704JJ93d6cU_2wxF7MJ2eF6bUeM22w0V5KJVvFKfnmTrEaBA2NCVlTsUJdizgkHM6WwsemxQk-cMivz37x5Mm9qqvna-vT8YNtv0L92XlRX4GQHYBXyEDCZ7AKODn1IVaHxMbz54B-lgJNa</recordid><startdate>20120427</startdate><enddate>20120427</enddate><creator>Kim, Se Hyun</creator><creator>Shin, Soon Young</creator><creator>Lee, Kyu Young</creator><creator>Joo, Eun Jeong</creator><creator>Song, Joo Youn</creator><creator>Ahn, Yong Min</creator><creator>Lee, Young Han</creator><creator>Kim, Yong Sik</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>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20120427</creationdate><title>The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity</title><author>Kim, Se Hyun ; Shin, Soon Young ; Lee, Kyu Young ; Joo, Eun Jeong ; Song, Joo Youn ; Ahn, Yong Min ; Lee, Young Han ; Kim, Yong Sik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-3d455fdcb0c90fa0f3cc5d9487375e6d379c1076a928ba55591c26829418282d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Alleles</topic><topic>Bipolar disorder</topic><topic>Bipolar Disorder - enzymology</topic><topic>Bipolar Disorder - genetics</topic><topic>Brain</topic><topic>Dual Specificity Phosphatase 6 - genetics</topic><topic>Dual-specificity phosphatase 6</topic><topic>Enzyme Activation - genetics</topic><topic>Enzyme Activation - physiology</topic><topic>Extracellular signal-regulated kinase</topic><topic>Female</topic><topic>Gene frequency</topic><topic>Genetic association</topic><topic>Genetic Association Studies - methods</topic><topic>Haplotypes</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Intracellular signalling</topic><topic>Leu114Val polymorphism</topic><topic>Lithium</topic><topic>Male</topic><topic>MAP Kinase Signaling System - genetics</topic><topic>MAP Kinase Signaling System - physiology</topic><topic>Mental disorders</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Phosphorylation</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Schizophrenia</topic><topic>Ser144Ala polymorphism</topic><topic>Single-nucleotide polymorphism</topic><topic>Transcription</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Se Hyun</creatorcontrib><creatorcontrib>Shin, Soon Young</creatorcontrib><creatorcontrib>Lee, Kyu Young</creatorcontrib><creatorcontrib>Joo, Eun Jeong</creatorcontrib><creatorcontrib>Song, Joo Youn</creatorcontrib><creatorcontrib>Ahn, Yong Min</creatorcontrib><creatorcontrib>Lee, Young Han</creatorcontrib><creatorcontrib>Kim, Yong Sik</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Se Hyun</au><au>Shin, Soon Young</au><au>Lee, Kyu Young</au><au>Joo, Eun Jeong</au><au>Song, Joo Youn</au><au>Ahn, Yong Min</au><au>Lee, Young Han</au><au>Kim, Yong Sik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity</atitle><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><date>2012-04-27</date><risdate>2012</risdate><volume>37</volume><issue>1</issue><spage>41</spage><epage>49</epage><pages>41-49</pages><issn>0278-5846</issn><eissn>1878-4216</eissn><abstract>The dual-specificity phosphatase 6 (DUSP6) gene resides at chromosome location 12q22–23, which is one of the candidate loci for susceptibility to bipolar disorder and which encodes a phosphatase selective for extracellular signal-regulated kinase (ERK). Previously, we reported a positive association between the functional Leu114Val polymorphism (rs2279574) in DUSP6 and bipolar disorder. Given that the association between DUSP6 and the reported down-regulation of DUSP6 transcript in bipolar postmortem brains were sex-dimorphic, showing significance in women but not men, we performed two independent analyses in homogenous samples of male and female Korean patients with bipolar disorder or schizophrenia using samples enlarged from our previous report. Among the examined DUSP6 SNPs, five (rs769700, rs704076, rs770087, rs808820, and rs2279574) showed positive allelic associations, with the frequency of minor alleles (C, T, G, G, and G) in each SNP significantly increased in women with BD. Consequently, the “C-T-G-G-G” haplotype was significantly over-represented (P=0.016; OR=3.242), whereas the “T-G-T-A-T” haplotype was significantly under-represented (P=0.014; OR=0.697). We found no significant associations with DUSP6 SNPs in men with bipolar disorder or schizophrenia. We also investigated the functions of the functional SNPs' positive associations and found that Leu114Val (rs2279574; T/G) and Ser144Ala (rs770087; T/G) mutations in DUSP6 proteins reduced lithium-induced ERK1/2 phosphorylation in vitro, implicating the dominant active functions. Thus, DUSP6 may not only play important roles in the pathogenesis of bipolar disorder, particularly in women, but also affect the therapeutic response to lithium through modulating lithium's effects on intracellular signaling.
► DUSP6 gene is shown to be associated with BD in Korea. ► Association between DUSP6 and BD is found in female patients. ► Leu114Val or Ser144Ala mutation of DUSP6 blunts the ERK activation by lithium.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>22155192</pmid><doi>10.1016/j.pnpbp.2011.11.014</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0278-5846 |
ispartof | Progress in neuro-psychopharmacology & biological psychiatry, 2012-04, Vol.37 (1), p.41-49 |
issn | 0278-5846 1878-4216 |
language | eng |
recordid | cdi_proquest_miscellaneous_926503762 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adult Alleles Bipolar disorder Bipolar Disorder - enzymology Bipolar Disorder - genetics Brain Dual Specificity Phosphatase 6 - genetics Dual-specificity phosphatase 6 Enzyme Activation - genetics Enzyme Activation - physiology Extracellular signal-regulated kinase Female Gene frequency Genetic association Genetic Association Studies - methods Haplotypes HeLa Cells Humans Intracellular signalling Leu114Val polymorphism Lithium Male MAP Kinase Signaling System - genetics MAP Kinase Signaling System - physiology Mental disorders Middle Aged Mutation Phosphorylation Polymorphism, Single Nucleotide - genetics Schizophrenia Ser144Ala polymorphism Single-nucleotide polymorphism Transcription Young Adult |
title | The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T04%3A34%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20genetic%20association%20of%20DUSP6%20with%20bipolar%20disorder%20and%20its%20effect%20on%20ERK%20activity&rft.jtitle=Progress%20in%20neuro-psychopharmacology%20&%20biological%20psychiatry&rft.au=Kim,%20Se%20Hyun&rft.date=2012-04-27&rft.volume=37&rft.issue=1&rft.spage=41&rft.epage=49&rft.pages=41-49&rft.issn=0278-5846&rft.eissn=1878-4216&rft_id=info:doi/10.1016/j.pnpbp.2011.11.014&rft_dat=%3Cproquest_cross%3E1011210035%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1011210035&rft_id=info:pmid/22155192&rft_els_id=S0278584611003447&rfr_iscdi=true |