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Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases
The role of the blood–brain barrier (BBB) in Alzheimer’s and other neurodegenerative diseases is still the subject of many studies. However, those studies using high-throughput methods have been compromised by the lack of Gene Ontology (GO) annotations describing the role of proteins in the normal f...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546235/ https://www.ncbi.nlm.nih.gov/pubmed/34697638 http://dx.doi.org/10.1093/database/baab067 |
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author | Saverimuttu, Shirin C C Kramarz, Barbara Rodríguez-López, Milagros Garmiri, Penelope Attrill, Helen Thurlow, Katherine E Makris, Marios de Miranda Pinheiro, Sandra Orchard, Sandra Lovering, Ruth C |
author_facet | Saverimuttu, Shirin C C Kramarz, Barbara Rodríguez-López, Milagros Garmiri, Penelope Attrill, Helen Thurlow, Katherine E Makris, Marios de Miranda Pinheiro, Sandra Orchard, Sandra Lovering, Ruth C |
author_sort | Saverimuttu, Shirin C C |
collection | PubMed |
description | The role of the blood–brain barrier (BBB) in Alzheimer’s and other neurodegenerative diseases is still the subject of many studies. However, those studies using high-throughput methods have been compromised by the lack of Gene Ontology (GO) annotations describing the role of proteins in the normal function of the BBB. The GO Consortium provides a gold-standard bioinformatics resource used for analysis and interpretation of large biomedical data sets. However, the GO is also used by other research communities and, therefore, must meet a variety of demands on the breadth and depth of information that is provided. To meet the needs of the Alzheimer’s research community we have focused on the GO annotation of the BBB, with over 100 transport or junctional proteins prioritized for annotation. This project has led to a substantial increase in the number of human proteins associated with BBB-relevant GO terms as well as more comprehensive annotation of these proteins in many other processes. Furthermore, data describing the microRNAs that regulate the expression of these priority proteins have also been curated. Thus, this project has increased both the breadth and depth of annotation for these prioritized BBB proteins. Database URLhttps://www.ebi.ac.uk/QuickGO/ |
format | Online Article Text |
id | pubmed-8546235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85462352021-10-26 Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases Saverimuttu, Shirin C C Kramarz, Barbara Rodríguez-López, Milagros Garmiri, Penelope Attrill, Helen Thurlow, Katherine E Makris, Marios de Miranda Pinheiro, Sandra Orchard, Sandra Lovering, Ruth C Database (Oxford) Original Article The role of the blood–brain barrier (BBB) in Alzheimer’s and other neurodegenerative diseases is still the subject of many studies. However, those studies using high-throughput methods have been compromised by the lack of Gene Ontology (GO) annotations describing the role of proteins in the normal function of the BBB. The GO Consortium provides a gold-standard bioinformatics resource used for analysis and interpretation of large biomedical data sets. However, the GO is also used by other research communities and, therefore, must meet a variety of demands on the breadth and depth of information that is provided. To meet the needs of the Alzheimer’s research community we have focused on the GO annotation of the BBB, with over 100 transport or junctional proteins prioritized for annotation. This project has led to a substantial increase in the number of human proteins associated with BBB-relevant GO terms as well as more comprehensive annotation of these proteins in many other processes. Furthermore, data describing the microRNAs that regulate the expression of these priority proteins have also been curated. Thus, this project has increased both the breadth and depth of annotation for these prioritized BBB proteins. Database URLhttps://www.ebi.ac.uk/QuickGO/ Oxford University Press 2021-10-26 /pmc/articles/PMC8546235/ /pubmed/34697638 http://dx.doi.org/10.1093/database/baab067 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Saverimuttu, Shirin C C Kramarz, Barbara Rodríguez-López, Milagros Garmiri, Penelope Attrill, Helen Thurlow, Katherine E Makris, Marios de Miranda Pinheiro, Sandra Orchard, Sandra Lovering, Ruth C Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title | Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title_full | Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title_fullStr | Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title_full_unstemmed | Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title_short | Gene Ontology curation of the blood–brain barrier to improve the analysis of Alzheimer’s and other neurological diseases |
title_sort | gene ontology curation of the blood–brain barrier to improve the analysis of alzheimer’s and other neurological diseases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546235/ https://www.ncbi.nlm.nih.gov/pubmed/34697638 http://dx.doi.org/10.1093/database/baab067 |
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