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A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband
Schizophrenia is a debilitating mental disorder affecting approximately 1% of the world's population. Childhood onset schizophrenia (COS), defined as onset before age 13, is a rare and severe form of the illness that may have more salient genetic influence. We identified a ~134 kb duplication s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447216/ https://www.ncbi.nlm.nih.gov/pubmed/23074677 http://dx.doi.org/10.1155/2011/585893 |
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author | Wilson, Nicole K. A. Lee, Yohan Long, Robert Hermetz, Karen Rudd, M. Katharine Miller, Rachel Rapoport, Judith L. Addington, Anjené M. |
author_facet | Wilson, Nicole K. A. Lee, Yohan Long, Robert Hermetz, Karen Rudd, M. Katharine Miller, Rachel Rapoport, Judith L. Addington, Anjené M. |
author_sort | Wilson, Nicole K. A. |
collection | PubMed |
description | Schizophrenia is a debilitating mental disorder affecting approximately 1% of the world's population. Childhood onset schizophrenia (COS), defined as onset before age 13, is a rare and severe form of the illness that may have more salient genetic influence. We identified a ~134 kb duplication spanning exons 2–4 of the Slit-Robo GTPase-activating protein 3 (SRGAP3) gene on chromosome 3p25.3 that tracks with psychotic illness in the family of a COS proband. Cloning and sequencing of the duplication junction confirmed that the duplication is tandem, and analysis of the resulting mRNA transcript suggests that the duplication would result in a frame shift mutation. This is the first family report of a SRGAP3 copy number variant (CNV) in schizophrenia. Considering that SRGAP3 is important in neural development, we conclude that this SRGAP3 duplication may be an important factor contributing to the psychotic phenotype in this family. |
format | Online Article Text |
id | pubmed-3447216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34472162012-10-16 A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband Wilson, Nicole K. A. Lee, Yohan Long, Robert Hermetz, Karen Rudd, M. Katharine Miller, Rachel Rapoport, Judith L. Addington, Anjené M. Case Rep Genet Case Report Schizophrenia is a debilitating mental disorder affecting approximately 1% of the world's population. Childhood onset schizophrenia (COS), defined as onset before age 13, is a rare and severe form of the illness that may have more salient genetic influence. We identified a ~134 kb duplication spanning exons 2–4 of the Slit-Robo GTPase-activating protein 3 (SRGAP3) gene on chromosome 3p25.3 that tracks with psychotic illness in the family of a COS proband. Cloning and sequencing of the duplication junction confirmed that the duplication is tandem, and analysis of the resulting mRNA transcript suggests that the duplication would result in a frame shift mutation. This is the first family report of a SRGAP3 copy number variant (CNV) in schizophrenia. Considering that SRGAP3 is important in neural development, we conclude that this SRGAP3 duplication may be an important factor contributing to the psychotic phenotype in this family. Hindawi Publishing Corporation 2011 2011-09-12 /pmc/articles/PMC3447216/ /pubmed/23074677 http://dx.doi.org/10.1155/2011/585893 Text en Copyright © 2011 Nicole K. A. Wilson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Wilson, Nicole K. A. Lee, Yohan Long, Robert Hermetz, Karen Rudd, M. Katharine Miller, Rachel Rapoport, Judith L. Addington, Anjené M. A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title_full | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title_fullStr | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title_full_unstemmed | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title_short | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband |
title_sort | novel microduplication in the neurodevelopmental gene srgap3 that segregates with psychotic illness in the family of a cos proband |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447216/ https://www.ncbi.nlm.nih.gov/pubmed/23074677 http://dx.doi.org/10.1155/2011/585893 |
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