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Exploration into biomarker potential of region-specific brain gene co-expression networks
The human brain is a complex organ that consists of several regions each with a unique gene expression pattern. Our intent in this study was to construct a gene co-expression network (GCN) for the normal brain using RNA expression profiles from the Genotype-Tissue Expression (GTEx) project. The brai...
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/PMC7553962/ https://www.ncbi.nlm.nih.gov/pubmed/33051491 http://dx.doi.org/10.1038/s41598-020-73611-1 |
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author | Hang, Yuqing Aburidi, Mohammed Husain, Benafsh Hickman, Allison R. Poehlman, William L. Feltus, F. Alex |
author_facet | Hang, Yuqing Aburidi, Mohammed Husain, Benafsh Hickman, Allison R. Poehlman, William L. Feltus, F. Alex |
author_sort | Hang, Yuqing |
collection | PubMed |
description | The human brain is a complex organ that consists of several regions each with a unique gene expression pattern. Our intent in this study was to construct a gene co-expression network (GCN) for the normal brain using RNA expression profiles from the Genotype-Tissue Expression (GTEx) project. The brain GCN contains gene correlation relationships that are broadly present in the brain or specific to thirteen brain regions, which we later combined into six overarching brain mini-GCNs based on the brain’s structure. Using the expression profiles of brain region-specific GCN edges, we determined how well the brain region samples could be discriminated from each other, visually with t-SNE plots or quantitatively with the Gene Oracle deep learning classifier. Next, we tested these gene sets on their relevance to human tumors of brain and non-brain origin. Interestingly, we found that genes in the six brain mini-GCNs showed markedly higher mutation rates in tumors relative to matched sets of random genes. Further, we found that cortex genes subdivided Head and Neck Squamous Cell Carcinoma (HNSC) tumors and Pheochromocytoma and Paraganglioma (PCPG) tumors into distinct groups. The brain GCN and mini-GCNs are useful resources for the classification of brain regions and identification of biomarker genes for brain related phenotypes. |
format | Online Article Text |
id | pubmed-7553962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75539622020-10-14 Exploration into biomarker potential of region-specific brain gene co-expression networks Hang, Yuqing Aburidi, Mohammed Husain, Benafsh Hickman, Allison R. Poehlman, William L. Feltus, F. Alex Sci Rep Article The human brain is a complex organ that consists of several regions each with a unique gene expression pattern. Our intent in this study was to construct a gene co-expression network (GCN) for the normal brain using RNA expression profiles from the Genotype-Tissue Expression (GTEx) project. The brain GCN contains gene correlation relationships that are broadly present in the brain or specific to thirteen brain regions, which we later combined into six overarching brain mini-GCNs based on the brain’s structure. Using the expression profiles of brain region-specific GCN edges, we determined how well the brain region samples could be discriminated from each other, visually with t-SNE plots or quantitatively with the Gene Oracle deep learning classifier. Next, we tested these gene sets on their relevance to human tumors of brain and non-brain origin. Interestingly, we found that genes in the six brain mini-GCNs showed markedly higher mutation rates in tumors relative to matched sets of random genes. Further, we found that cortex genes subdivided Head and Neck Squamous Cell Carcinoma (HNSC) tumors and Pheochromocytoma and Paraganglioma (PCPG) tumors into distinct groups. The brain GCN and mini-GCNs are useful resources for the classification of brain regions and identification of biomarker genes for brain related phenotypes. Nature Publishing Group UK 2020-10-13 /pmc/articles/PMC7553962/ /pubmed/33051491 http://dx.doi.org/10.1038/s41598-020-73611-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hang, Yuqing Aburidi, Mohammed Husain, Benafsh Hickman, Allison R. Poehlman, William L. Feltus, F. Alex Exploration into biomarker potential of region-specific brain gene co-expression networks |
title | Exploration into biomarker potential of region-specific brain gene co-expression networks |
title_full | Exploration into biomarker potential of region-specific brain gene co-expression networks |
title_fullStr | Exploration into biomarker potential of region-specific brain gene co-expression networks |
title_full_unstemmed | Exploration into biomarker potential of region-specific brain gene co-expression networks |
title_short | Exploration into biomarker potential of region-specific brain gene co-expression networks |
title_sort | exploration into biomarker potential of region-specific brain gene co-expression networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553962/ https://www.ncbi.nlm.nih.gov/pubmed/33051491 http://dx.doi.org/10.1038/s41598-020-73611-1 |
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