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ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies

BACKGROUND: The chromosome 22q11 region is proposed as a major candidate locus for susceptibility genes to schizophrenia. Recently, the gene ZDHHC8 encoding a putative palmitoyltransferase at 22q11 was proposed to increase liability to schizophrenia based on both animal models and human association...

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Autores principales: Faul, Thomas, Gawlik, Micha, Bauer, Martin, Jung, Sven, Pfuhlmann, Bruno, Jabs, Burkhard, Knapp, Michael, Stöber, Gerald
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1274335/
https://www.ncbi.nlm.nih.gov/pubmed/16225675
http://dx.doi.org/10.1186/1471-244X-5-35
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author Faul, Thomas
Gawlik, Micha
Bauer, Martin
Jung, Sven
Pfuhlmann, Bruno
Jabs, Burkhard
Knapp, Michael
Stöber, Gerald
author_facet Faul, Thomas
Gawlik, Micha
Bauer, Martin
Jung, Sven
Pfuhlmann, Bruno
Jabs, Burkhard
Knapp, Michael
Stöber, Gerald
author_sort Faul, Thomas
collection PubMed
description BACKGROUND: The chromosome 22q11 region is proposed as a major candidate locus for susceptibility genes to schizophrenia. Recently, the gene ZDHHC8 encoding a putative palmitoyltransferase at 22q11 was proposed to increase liability to schizophrenia based on both animal models and human association studies by significant over-transmission of allele rs175174A in female, but not male subjects with schizophrenia. METHODS: Given the genetic complexity of schizophrenia and the potential genetic heterogeneity in different populations, we examined rs175174 in 204 German proband-parent triads and in an independent case-control study (schizophrenic cases: n = 433; controls: n = 186). RESULTS: In the triads heterozygous parents transmitted allele G preferentially to females, and allele A to males (heterogeneity χ(2 )= 4.43; p = 0.035). The case-control sample provided no further evidence for overall or gender-specific effects regarding allele and genotype frequency distributions. CONCLUSION: The findings on rs175174 at ZDHHC8 are still far from being conclusive, but evidence for sexual dimorphism is moderate, and our data do not support a significant genetic contribution of rs175174 to the aetiopathogenesis of schizophrenia.
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spelling pubmed-12743352005-10-29 ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies Faul, Thomas Gawlik, Micha Bauer, Martin Jung, Sven Pfuhlmann, Bruno Jabs, Burkhard Knapp, Michael Stöber, Gerald BMC Psychiatry Research Article BACKGROUND: The chromosome 22q11 region is proposed as a major candidate locus for susceptibility genes to schizophrenia. Recently, the gene ZDHHC8 encoding a putative palmitoyltransferase at 22q11 was proposed to increase liability to schizophrenia based on both animal models and human association studies by significant over-transmission of allele rs175174A in female, but not male subjects with schizophrenia. METHODS: Given the genetic complexity of schizophrenia and the potential genetic heterogeneity in different populations, we examined rs175174 in 204 German proband-parent triads and in an independent case-control study (schizophrenic cases: n = 433; controls: n = 186). RESULTS: In the triads heterozygous parents transmitted allele G preferentially to females, and allele A to males (heterogeneity χ(2 )= 4.43; p = 0.035). The case-control sample provided no further evidence for overall or gender-specific effects regarding allele and genotype frequency distributions. CONCLUSION: The findings on rs175174 at ZDHHC8 are still far from being conclusive, but evidence for sexual dimorphism is moderate, and our data do not support a significant genetic contribution of rs175174 to the aetiopathogenesis of schizophrenia. BioMed Central 2005-10-14 /pmc/articles/PMC1274335/ /pubmed/16225675 http://dx.doi.org/10.1186/1471-244X-5-35 Text en Copyright © 2005 Faul et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Faul, Thomas
Gawlik, Micha
Bauer, Martin
Jung, Sven
Pfuhlmann, Bruno
Jabs, Burkhard
Knapp, Michael
Stöber, Gerald
ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title_full ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title_fullStr ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title_full_unstemmed ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title_short ZDHHC8 as a candidate gene for schizophrenia: Analysis of a putative functional intronic marker in case-control and family-based association studies
title_sort zdhhc8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1274335/
https://www.ncbi.nlm.nih.gov/pubmed/16225675
http://dx.doi.org/10.1186/1471-244X-5-35
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