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Next-generation profiling to identify the molecular etiology of Parkinson dementia
OBJECTIVE: We sought to determine the underlying cortical gene expression changes associated with Parkinson dementia using a next-generation RNA sequencing approach. METHODS: In this study, we used RNA sequencing to evaluate differential gene expression and alternative splicing in the posterior cing...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881621/ https://www.ncbi.nlm.nih.gov/pubmed/27275011 http://dx.doi.org/10.1212/NXG.0000000000000075 |
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author | Henderson-Smith, Adrienne Corneveaux, Jason J. De Both, Matthew Cuyugan, Lori Liang, Winnie S. Huentelman, Matthew Adler, Charles Driver-Dunckley, Erika Beach, Thomas G. Dunckley, Travis L. |
author_facet | Henderson-Smith, Adrienne Corneveaux, Jason J. De Both, Matthew Cuyugan, Lori Liang, Winnie S. Huentelman, Matthew Adler, Charles Driver-Dunckley, Erika Beach, Thomas G. Dunckley, Travis L. |
author_sort | Henderson-Smith, Adrienne |
collection | PubMed |
description | OBJECTIVE: We sought to determine the underlying cortical gene expression changes associated with Parkinson dementia using a next-generation RNA sequencing approach. METHODS: In this study, we used RNA sequencing to evaluate differential gene expression and alternative splicing in the posterior cingulate cortex from neurologically normal control patients, patients with Parkinson disease, and patients with Parkinson disease with dementia. RESULTS: Genes overexpressed in both disease states were involved with an immune response, whereas shared underexpressed genes functioned in signal transduction or as components of the cytoskeleton. Alternative splicing analysis produced a pattern of immune and RNA-processing disturbances. CONCLUSIONS: Genes with the greatest degree of differential expression did not overlap with genes exhibiting significant alternative splicing activity. Such variation indicates the importance of broadening expression studies to include exon-level changes because there can be significant differential splicing activity with potential structural consequences, a subtlety that is not detected when examining differential gene expression alone, or is underrepresented with probe-limited array technology. |
format | Online Article Text |
id | pubmed-4881621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-48816212016-06-03 Next-generation profiling to identify the molecular etiology of Parkinson dementia Henderson-Smith, Adrienne Corneveaux, Jason J. De Both, Matthew Cuyugan, Lori Liang, Winnie S. Huentelman, Matthew Adler, Charles Driver-Dunckley, Erika Beach, Thomas G. Dunckley, Travis L. Neurol Genet Article OBJECTIVE: We sought to determine the underlying cortical gene expression changes associated with Parkinson dementia using a next-generation RNA sequencing approach. METHODS: In this study, we used RNA sequencing to evaluate differential gene expression and alternative splicing in the posterior cingulate cortex from neurologically normal control patients, patients with Parkinson disease, and patients with Parkinson disease with dementia. RESULTS: Genes overexpressed in both disease states were involved with an immune response, whereas shared underexpressed genes functioned in signal transduction or as components of the cytoskeleton. Alternative splicing analysis produced a pattern of immune and RNA-processing disturbances. CONCLUSIONS: Genes with the greatest degree of differential expression did not overlap with genes exhibiting significant alternative splicing activity. Such variation indicates the importance of broadening expression studies to include exon-level changes because there can be significant differential splicing activity with potential structural consequences, a subtlety that is not detected when examining differential gene expression alone, or is underrepresented with probe-limited array technology. Wolters Kluwer 2016-05-24 /pmc/articles/PMC4881621/ /pubmed/27275011 http://dx.doi.org/10.1212/NXG.0000000000000075 Text en © 2016 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Article Henderson-Smith, Adrienne Corneveaux, Jason J. De Both, Matthew Cuyugan, Lori Liang, Winnie S. Huentelman, Matthew Adler, Charles Driver-Dunckley, Erika Beach, Thomas G. Dunckley, Travis L. Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title | Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title_full | Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title_fullStr | Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title_full_unstemmed | Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title_short | Next-generation profiling to identify the molecular etiology of Parkinson dementia |
title_sort | next-generation profiling to identify the molecular etiology of parkinson dementia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881621/ https://www.ncbi.nlm.nih.gov/pubmed/27275011 http://dx.doi.org/10.1212/NXG.0000000000000075 |
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