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Functional validation of CHMP7 as an ADHD risk gene
Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder of childhood with a strong genetic component. Despite the success of mapping ADHD risk loci, little work has been done to experimentally verify the contribution of these loci to ADHD phenotypes. Meta-analysis of four ge...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648633/ https://www.ncbi.nlm.nih.gov/pubmed/33159045 http://dx.doi.org/10.1038/s41398-020-01077-w |
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author | Dark, Callum Williams, Caitlin Bellgrove, Mark A. Hawi, Ziarih Bryson-Richardson, Robert J. |
author_facet | Dark, Callum Williams, Caitlin Bellgrove, Mark A. Hawi, Ziarih Bryson-Richardson, Robert J. |
author_sort | Dark, Callum |
collection | PubMed |
description | Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder of childhood with a strong genetic component. Despite the success of mapping ADHD risk loci, little work has been done to experimentally verify the contribution of these loci to ADHD phenotypes. Meta-analysis of four genome-wide association studies in ADHD suggested CHMP7 as a predisposing gene for ADHD. A DNA variant (rs2294123) mapped to CHMP7 has been shown (via bioinformatic analysis) to have a high likelihood for functionality and correlate with reduced transcript levels. We used CRISPR-Cas9 genome editing to generate a chmp7 zebrafish model for ADHD. chmp7(+/−) fish showed comparable reductions in mRNA levels to individuals homozygous for the CHMP7 ADHD risk allele. These fish displayed significant hyperactivity over a 24-h period at 6 days post-fertilisation compared to chmp7(+/+), but this effect did not persist into juvenile and adulthood stages. In addition, chmp7(+/−) fish had significantly smaller total brain volumes than chmp7(+/+) fish. Finally, the hyperactivity at 6 days post-fertilisation was significantly reduced through the application of methylphenidate, a mainstay pharmacological treatment for ADHD. Overall, this study highlights an important role for CHMP7 in the neurodevelopment of ADHD, and demonstrates the utility of zebrafish for modelling the functional effects of genes conferring risk to ADHD. |
format | Online Article Text |
id | pubmed-7648633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76486332020-11-09 Functional validation of CHMP7 as an ADHD risk gene Dark, Callum Williams, Caitlin Bellgrove, Mark A. Hawi, Ziarih Bryson-Richardson, Robert J. Transl Psychiatry Article Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder of childhood with a strong genetic component. Despite the success of mapping ADHD risk loci, little work has been done to experimentally verify the contribution of these loci to ADHD phenotypes. Meta-analysis of four genome-wide association studies in ADHD suggested CHMP7 as a predisposing gene for ADHD. A DNA variant (rs2294123) mapped to CHMP7 has been shown (via bioinformatic analysis) to have a high likelihood for functionality and correlate with reduced transcript levels. We used CRISPR-Cas9 genome editing to generate a chmp7 zebrafish model for ADHD. chmp7(+/−) fish showed comparable reductions in mRNA levels to individuals homozygous for the CHMP7 ADHD risk allele. These fish displayed significant hyperactivity over a 24-h period at 6 days post-fertilisation compared to chmp7(+/+), but this effect did not persist into juvenile and adulthood stages. In addition, chmp7(+/−) fish had significantly smaller total brain volumes than chmp7(+/+) fish. Finally, the hyperactivity at 6 days post-fertilisation was significantly reduced through the application of methylphenidate, a mainstay pharmacological treatment for ADHD. Overall, this study highlights an important role for CHMP7 in the neurodevelopment of ADHD, and demonstrates the utility of zebrafish for modelling the functional effects of genes conferring risk to ADHD. Nature Publishing Group UK 2020-11-06 /pmc/articles/PMC7648633/ /pubmed/33159045 http://dx.doi.org/10.1038/s41398-020-01077-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dark, Callum Williams, Caitlin Bellgrove, Mark A. Hawi, Ziarih Bryson-Richardson, Robert J. Functional validation of CHMP7 as an ADHD risk gene |
title | Functional validation of CHMP7 as an ADHD risk gene |
title_full | Functional validation of CHMP7 as an ADHD risk gene |
title_fullStr | Functional validation of CHMP7 as an ADHD risk gene |
title_full_unstemmed | Functional validation of CHMP7 as an ADHD risk gene |
title_short | Functional validation of CHMP7 as an ADHD risk gene |
title_sort | functional validation of chmp7 as an adhd risk gene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648633/ https://www.ncbi.nlm.nih.gov/pubmed/33159045 http://dx.doi.org/10.1038/s41398-020-01077-w |
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