Association of 14-3-3 ε gene haplotype with completed suicide in Japanese
Genetic factors have been suggested to be involved in suicide. Although some genetic factors, such as serotonergic transduction, have been associated with suicide, the results are inconsistent. There is a possibility that various signaling anomalies are involved in the biological vulnerability to su...
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creator | Yanagi, Masaya Shirakawa, Osamu Kitamura, Noboru Okamura, Kenji Sakurai, Kaoru Nishiguchi, Naoki Hashimoto, Takeshi Nushida, Hideyuki Ueno, Yasuhiro Kanbe, Daiji Kawamura, Meiko Araki, Kazuaki Nawa, Hiroyuki Maeda, Kiyoshi |
description | Genetic factors have been suggested to be involved in suicide. Although some genetic factors, such as serotonergic transduction, have been associated with suicide, the results are inconsistent. There is a possibility that various signaling anomalies are involved in the biological vulnerability to suicide. We carried out a genome-wide gene-expression study in the brains of suicide victims using DNA microarrays;14-3-3 ε, which is related to neurogenesis, was one of the genes upregulated in the brains of suicide victims in the microarray analysis. This was confirmed by Western blot analysis. To examine the possibility of the involvement of 14-3-3 ε in the pathogenesis of suicide, we investigated the association of the 14-3-3 ε gene and completed suicide. We used three high-frequency SNPs (rs1532976, rs3752826, and rs9393) and found a significant association of two alleles (rs1532976 and rs3752826) with completed suicide (
p
< 0.05). Moreover, the distribution of haplotype revealed a more significant difference between completed suicide and controls (
p
=0.0005). This finding suggests that 14-3-3 ε is a potential suicide susceptibility gene and implies that dysregulation of neurogenesis may be involved in suicide. |
doi_str_mv | 10.1007/s10038-005-0241-0 |
format | Article |
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p
< 0.05). Moreover, the distribution of haplotype revealed a more significant difference between completed suicide and controls (
p
=0.0005). This finding suggests that 14-3-3 ε is a potential suicide susceptibility gene and implies that dysregulation of neurogenesis may be involved in suicide.</description><identifier>ISSN: 1434-5161</identifier><identifier>EISSN: 1435-232X</identifier><identifier>DOI: 10.1007/s10038-005-0241-0</identifier><identifier>PMID: 15838597</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>14-3-3 protein ; 14-3-3 Proteins - genetics ; Adult ; Aged ; Biomedicine ; DNA microarrays ; Female ; Gene Expression ; Gene Expression Profiling ; Gene Function ; Gene Therapy ; Genetic factors ; Genetic Predisposition to Disease ; Genomes ; Genotype ; Haplotypes ; Haplotypes - genetics ; Human Genetics ; Humans ; Japan ; Male ; Middle Aged ; Molecular Medicine ; Neurogenesis ; Oligonucleotide Array Sequence Analysis ; Original Article ; Polymorphism, Single Nucleotide - genetics ; Signal transduction ; Single-nucleotide polymorphism ; Suicide ; Suicide genes</subject><ispartof>Journal of human genetics, 2005-04, Vol.50 (4), p.210-216</ispartof><rights>The Japan Society of Human Genetics and Springer-Verlag 2005</rights><rights>The Japan Society of Human Genetics and Springer-Verlag 2005.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-473a55da0dcf959e49621ec8b166891e66be12be08f5e3863808763ca58d815f3</citedby><cites>FETCH-LOGICAL-c437t-473a55da0dcf959e49621ec8b166891e66be12be08f5e3863808763ca58d815f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10038-005-0241-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10038-005-0241-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15838597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yanagi, Masaya</creatorcontrib><creatorcontrib>Shirakawa, Osamu</creatorcontrib><creatorcontrib>Kitamura, Noboru</creatorcontrib><creatorcontrib>Okamura, Kenji</creatorcontrib><creatorcontrib>Sakurai, Kaoru</creatorcontrib><creatorcontrib>Nishiguchi, Naoki</creatorcontrib><creatorcontrib>Hashimoto, Takeshi</creatorcontrib><creatorcontrib>Nushida, Hideyuki</creatorcontrib><creatorcontrib>Ueno, Yasuhiro</creatorcontrib><creatorcontrib>Kanbe, Daiji</creatorcontrib><creatorcontrib>Kawamura, Meiko</creatorcontrib><creatorcontrib>Araki, Kazuaki</creatorcontrib><creatorcontrib>Nawa, Hiroyuki</creatorcontrib><creatorcontrib>Maeda, Kiyoshi</creatorcontrib><title>Association of 14-3-3 ε gene haplotype with completed suicide in Japanese</title><title>Journal of human genetics</title><addtitle>J Hum Genet</addtitle><addtitle>J Hum Genet</addtitle><description>Genetic factors have been suggested to be involved in suicide. Although some genetic factors, such as serotonergic transduction, have been associated with suicide, the results are inconsistent. There is a possibility that various signaling anomalies are involved in the biological vulnerability to suicide. We carried out a genome-wide gene-expression study in the brains of suicide victims using DNA microarrays;14-3-3 ε, which is related to neurogenesis, was one of the genes upregulated in the brains of suicide victims in the microarray analysis. This was confirmed by Western blot analysis. To examine the possibility of the involvement of 14-3-3 ε in the pathogenesis of suicide, we investigated the association of the 14-3-3 ε gene and completed suicide. We used three high-frequency SNPs (rs1532976, rs3752826, and rs9393) and found a significant association of two alleles (rs1532976 and rs3752826) with completed suicide (
p
< 0.05). Moreover, the distribution of haplotype revealed a more significant difference between completed suicide and controls (
p
=0.0005). This finding suggests that 14-3-3 ε is a potential suicide susceptibility gene and implies that dysregulation of neurogenesis may be involved in suicide.</description><subject>14-3-3 protein</subject><subject>14-3-3 Proteins - genetics</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomedicine</subject><subject>DNA microarrays</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Function</subject><subject>Gene Therapy</subject><subject>Genetic factors</subject><subject>Genetic Predisposition to Disease</subject><subject>Genomes</subject><subject>Genotype</subject><subject>Haplotypes</subject><subject>Haplotypes - genetics</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Japan</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Neurogenesis</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Original Article</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Signal transduction</subject><subject>Single-nucleotide polymorphism</subject><subject>Suicide</subject><subject>Suicide genes</subject><issn>1434-5161</issn><issn>1435-232X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kM1KxDAQx4Mofqw-gBcJCN6imaRJ06OInwheFLyFbDp1u3Sb2rTIPpiv4TOZdRcEwUsmML_5z_Aj5Bj4OXCeX8T0SsM4V4yLDBjfIvuQScWEFK_bP_-MKdCwRw5inPNEi1zskj1QRhpV5Pvk4TLG4Gs31KGloaKQMckk_fqkb9ginbmuCcOyQ_pRDzPqw6JrcMCSxrH2dYm0bumD61yLEQ_JTuWaiEebOiEvN9fPV3fs8en2_urykflM5gPLcumUKh0vfVWoArNCC0BvpqC1KQC1niKIKXJTKZRGS8NNrqV3ypQGVCUn5Gyd2_XhfcQ42EUdPTZNuiKM0erccFEYmcDTP-A8jH2bbrMiE0qDzmFFwZryfYixx8p2fb1w_dICtyvNdq3ZJs12pdnyNHOySR6nCyx_JzZeEyDWQEyt9g3739X_p34Daz6FuA</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Yanagi, Masaya</creator><creator>Shirakawa, Osamu</creator><creator>Kitamura, Noboru</creator><creator>Okamura, Kenji</creator><creator>Sakurai, Kaoru</creator><creator>Nishiguchi, Naoki</creator><creator>Hashimoto, Takeshi</creator><creator>Nushida, Hideyuki</creator><creator>Ueno, Yasuhiro</creator><creator>Kanbe, Daiji</creator><creator>Kawamura, Meiko</creator><creator>Araki, Kazuaki</creator><creator>Nawa, Hiroyuki</creator><creator>Maeda, Kiyoshi</creator><general>Springer Japan</general><general>Nature Publishing Group</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20050401</creationdate><title>Association of 14-3-3 ε gene haplotype with completed suicide in Japanese</title><author>Yanagi, Masaya ; Shirakawa, Osamu ; Kitamura, Noboru ; Okamura, Kenji ; Sakurai, Kaoru ; Nishiguchi, Naoki ; Hashimoto, Takeshi ; Nushida, Hideyuki ; Ueno, Yasuhiro ; Kanbe, Daiji ; Kawamura, Meiko ; Araki, Kazuaki ; Nawa, Hiroyuki ; Maeda, Kiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-473a55da0dcf959e49621ec8b166891e66be12be08f5e3863808763ca58d815f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>14-3-3 protein</topic><topic>14-3-3 Proteins - 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Academic</collection><jtitle>Journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yanagi, Masaya</au><au>Shirakawa, Osamu</au><au>Kitamura, Noboru</au><au>Okamura, Kenji</au><au>Sakurai, Kaoru</au><au>Nishiguchi, Naoki</au><au>Hashimoto, Takeshi</au><au>Nushida, Hideyuki</au><au>Ueno, Yasuhiro</au><au>Kanbe, Daiji</au><au>Kawamura, Meiko</au><au>Araki, Kazuaki</au><au>Nawa, Hiroyuki</au><au>Maeda, Kiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of 14-3-3 ε gene haplotype with completed suicide in Japanese</atitle><jtitle>Journal of human genetics</jtitle><stitle>J Hum Genet</stitle><addtitle>J Hum Genet</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>50</volume><issue>4</issue><spage>210</spage><epage>216</epage><pages>210-216</pages><issn>1434-5161</issn><eissn>1435-232X</eissn><abstract>Genetic factors have been suggested to be involved in suicide. Although some genetic factors, such as serotonergic transduction, have been associated with suicide, the results are inconsistent. There is a possibility that various signaling anomalies are involved in the biological vulnerability to suicide. We carried out a genome-wide gene-expression study in the brains of suicide victims using DNA microarrays;14-3-3 ε, which is related to neurogenesis, was one of the genes upregulated in the brains of suicide victims in the microarray analysis. This was confirmed by Western blot analysis. To examine the possibility of the involvement of 14-3-3 ε in the pathogenesis of suicide, we investigated the association of the 14-3-3 ε gene and completed suicide. We used three high-frequency SNPs (rs1532976, rs3752826, and rs9393) and found a significant association of two alleles (rs1532976 and rs3752826) with completed suicide (
p
< 0.05). Moreover, the distribution of haplotype revealed a more significant difference between completed suicide and controls (
p
=0.0005). This finding suggests that 14-3-3 ε is a potential suicide susceptibility gene and implies that dysregulation of neurogenesis may be involved in suicide.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>15838597</pmid><doi>10.1007/s10038-005-0241-0</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 14-3-3 protein 14-3-3 Proteins - genetics Adult Aged Biomedicine DNA microarrays Female Gene Expression Gene Expression Profiling Gene Function Gene Therapy Genetic factors Genetic Predisposition to Disease Genomes Genotype Haplotypes Haplotypes - genetics Human Genetics Humans Japan Male Middle Aged Molecular Medicine Neurogenesis Oligonucleotide Array Sequence Analysis Original Article Polymorphism, Single Nucleotide - genetics Signal transduction Single-nucleotide polymorphism Suicide Suicide genes |
title | Association of 14-3-3 ε gene haplotype with completed suicide in Japanese |
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