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Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia
Voltage-gated L-type calcium channels (VLCC) are distributed widely throughout the brain. Among the genes involved in schizophrenia (SCZ), genes encoding VLCC subunits have attracted widespread attention. Among the four subunits comprising the VLCC (α − 1, α −2/δ, β, and γ), the γ subunit that compr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840350/ https://www.ncbi.nlm.nih.gov/pubmed/27102562 http://dx.doi.org/10.1038/srep24914 |
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author | Guan, Fanglin Zhang, Tianxiao Liu, Xinshe Han, Wei Lin, Huali Li, Lu Chen, Gang Li, Tao |
author_facet | Guan, Fanglin Zhang, Tianxiao Liu, Xinshe Han, Wei Lin, Huali Li, Lu Chen, Gang Li, Tao |
author_sort | Guan, Fanglin |
collection | PubMed |
description | Voltage-gated L-type calcium channels (VLCC) are distributed widely throughout the brain. Among the genes involved in schizophrenia (SCZ), genes encoding VLCC subunits have attracted widespread attention. Among the four subunits comprising the VLCC (α − 1, α −2/δ, β, and γ), the γ subunit that comprises an eight-member protein family is the least well understood. In our study, to further investigate the risk susceptibility by the γ subunit gene family to SCZ, we conducted a large-scale association study in Han Chinese individuals. The SNP rs17645023 located in the intergenic region of CACNG4 and CACNG5 was identified to be significantly associated with SCZ (OR = 0.856, P = 5.43 × 10(−5)). Similar results were obtained in the meta-analysis with the current SCZ PGC data (OR = 0.8853). We also identified a two-SNP haplotype (rs10420331-rs11084307, P = 1.4 × 10(−6)) covering the intronic region of CACNG8 to be significantly associated with SCZ. Epistasis analyses were conducted, and significant statistical interaction (OR = 0.622, P = 2.93 × 10(−6), P(perm) < 0.001) was observed between rs192808 (CACNG6) and rs2048137 (CACNG5). Our results indicate that CACNG4, CACNG5, CACNG6 and CACNG8 may contribute to the risk of SCZ. The statistical epistasis identified between CACNG5 and CACNG6 suggests that there may be an underlying biological interaction between the two genes. |
format | Online Article Text |
id | pubmed-4840350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48403502016-04-28 Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia Guan, Fanglin Zhang, Tianxiao Liu, Xinshe Han, Wei Lin, Huali Li, Lu Chen, Gang Li, Tao Sci Rep Article Voltage-gated L-type calcium channels (VLCC) are distributed widely throughout the brain. Among the genes involved in schizophrenia (SCZ), genes encoding VLCC subunits have attracted widespread attention. Among the four subunits comprising the VLCC (α − 1, α −2/δ, β, and γ), the γ subunit that comprises an eight-member protein family is the least well understood. In our study, to further investigate the risk susceptibility by the γ subunit gene family to SCZ, we conducted a large-scale association study in Han Chinese individuals. The SNP rs17645023 located in the intergenic region of CACNG4 and CACNG5 was identified to be significantly associated with SCZ (OR = 0.856, P = 5.43 × 10(−5)). Similar results were obtained in the meta-analysis with the current SCZ PGC data (OR = 0.8853). We also identified a two-SNP haplotype (rs10420331-rs11084307, P = 1.4 × 10(−6)) covering the intronic region of CACNG8 to be significantly associated with SCZ. Epistasis analyses were conducted, and significant statistical interaction (OR = 0.622, P = 2.93 × 10(−6), P(perm) < 0.001) was observed between rs192808 (CACNG6) and rs2048137 (CACNG5). Our results indicate that CACNG4, CACNG5, CACNG6 and CACNG8 may contribute to the risk of SCZ. The statistical epistasis identified between CACNG5 and CACNG6 suggests that there may be an underlying biological interaction between the two genes. Nature Publishing Group 2016-04-22 /pmc/articles/PMC4840350/ /pubmed/27102562 http://dx.doi.org/10.1038/srep24914 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Guan, Fanglin Zhang, Tianxiao Liu, Xinshe Han, Wei Lin, Huali Li, Lu Chen, Gang Li, Tao Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title | Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title_full | Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title_fullStr | Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title_full_unstemmed | Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title_short | Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
title_sort | evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840350/ https://www.ncbi.nlm.nih.gov/pubmed/27102562 http://dx.doi.org/10.1038/srep24914 |
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