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Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease
OBJECTIVES: In order to determine how gene expression is altered in disease it is of fundamental importance that the global distribution of gene expression levels across the disease-free brain are understood and how differences between tissue types might inform tissue choice for investigation of alt...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123947/ https://www.ncbi.nlm.nih.gov/pubmed/30180886 http://dx.doi.org/10.1186/s13104-018-3732-8 |
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author | Chappell, Sally Patel, Tulsi Guetta-Baranes, Tamar Sang, Fei Francis, Paul T. Morgan, Kevin Brookes, Keeley J. |
author_facet | Chappell, Sally Patel, Tulsi Guetta-Baranes, Tamar Sang, Fei Francis, Paul T. Morgan, Kevin Brookes, Keeley J. |
author_sort | Chappell, Sally |
collection | PubMed |
description | OBJECTIVES: In order to determine how gene expression is altered in disease it is of fundamental importance that the global distribution of gene expression levels across the disease-free brain are understood and how differences between tissue types might inform tissue choice for investigation of altered expression in disease state. The aim of this pilot project was to use RNA-sequencing to investigate gene expression differences between five general areas of post-mortem human brain (frontal, temporal, occipital, parietal and cerebellum), and in particular changes in gene expression in the cerebellum compared to cortex regions for genes relevant to Alzheimer’s disease, as the cerebellum is largely preserved from disease pathology and could be an area of interest for neuroprotective pathways. RESULTS: General gene expression profiles were found to be similar between cortical regions of the brain, however the cerebellum presented a distinct expression profile. Focused exploration of gene expression for genes associated with Alzheimer’s disease suggest that those involved in the immunity pathway show little expression in the brain. Furthermore some Alzheimer’s disease associated genes display significantly different expression in the cerebellum compared with other brain regions, which might indicate potential neuroprotective measures. |
format | Online Article Text |
id | pubmed-6123947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61239472018-09-10 Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease Chappell, Sally Patel, Tulsi Guetta-Baranes, Tamar Sang, Fei Francis, Paul T. Morgan, Kevin Brookes, Keeley J. BMC Res Notes Research Note OBJECTIVES: In order to determine how gene expression is altered in disease it is of fundamental importance that the global distribution of gene expression levels across the disease-free brain are understood and how differences between tissue types might inform tissue choice for investigation of altered expression in disease state. The aim of this pilot project was to use RNA-sequencing to investigate gene expression differences between five general areas of post-mortem human brain (frontal, temporal, occipital, parietal and cerebellum), and in particular changes in gene expression in the cerebellum compared to cortex regions for genes relevant to Alzheimer’s disease, as the cerebellum is largely preserved from disease pathology and could be an area of interest for neuroprotective pathways. RESULTS: General gene expression profiles were found to be similar between cortical regions of the brain, however the cerebellum presented a distinct expression profile. Focused exploration of gene expression for genes associated with Alzheimer’s disease suggest that those involved in the immunity pathway show little expression in the brain. Furthermore some Alzheimer’s disease associated genes display significantly different expression in the cerebellum compared with other brain regions, which might indicate potential neuroprotective measures. BioMed Central 2018-09-04 /pmc/articles/PMC6123947/ /pubmed/30180886 http://dx.doi.org/10.1186/s13104-018-3732-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Chappell, Sally Patel, Tulsi Guetta-Baranes, Tamar Sang, Fei Francis, Paul T. Morgan, Kevin Brookes, Keeley J. Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title | Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title_full | Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title_fullStr | Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title_full_unstemmed | Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title_short | Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer’s disease |
title_sort | observations of extensive gene expression differences in the cerebellum and potential relevance to alzheimer’s disease |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123947/ https://www.ncbi.nlm.nih.gov/pubmed/30180886 http://dx.doi.org/10.1186/s13104-018-3732-8 |
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