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Sensing the cilium, digital capture of ciliary data for comparative genomics investigations

BACKGROUND: Cilia are specialized, hair-like structures that project from the cell bodies of eukaryotic cells. With increased understanding of the distribution and functions of various types of cilia, interest in these organelles is accelerating. To effectively use this great expansion in knowledge,...

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Autores principales: Christie, Karen R., Blake, Judith A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907423/
https://www.ncbi.nlm.nih.gov/pubmed/29713460
http://dx.doi.org/10.1186/s13630-018-0057-0
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author Christie, Karen R.
Blake, Judith A.
author_facet Christie, Karen R.
Blake, Judith A.
author_sort Christie, Karen R.
collection PubMed
description BACKGROUND: Cilia are specialized, hair-like structures that project from the cell bodies of eukaryotic cells. With increased understanding of the distribution and functions of various types of cilia, interest in these organelles is accelerating. To effectively use this great expansion in knowledge, this information must be made digitally accessible and available for large-scale analytical and computational investigation. Capture and integration of knowledge about cilia into existing knowledge bases, thus providing the ability to improve comparative genomic data analysis, is the objective of this work. METHODS: We focused on the capture of information about cilia as studied in the laboratory mouse, a primary model of human biology. The workflow developed establishes a standard for capture of comparative functional data relevant to human biology. We established the 310 closest mouse orthologs of the 302 human genes defined in the SYSCILIA Gold Standard set of ciliary genes. For the mouse genes, we identified biomedical literature for curation and used Gene Ontology (GO) curation paradigms to provide functional annotations from these publications. RESULTS: Employing a methodology for comprehensive capture of experimental data about cilia genes in structured, digital form, we established a workflow for curation of experimental literature detailing molecular function and roles of cilia proteins starting with the mouse orthologs of the human SYSCILIA gene set. We worked closely with the GO Consortium ontology development editors and the SYSCILIA Consortium to improve the representation of ciliary biology within the GO. During the time frame of the ontology improvement project, we have fully curated 134 of these 310 mouse genes, resulting in an increase in the number of ciliary and other experimental annotations. CONCLUSIONS: We have improved the GO annotations available for mouse genes orthologous to the human genes in the SYSCILIA Consortium’s Gold Standard set. In addition, ciliary terminology in the GO itself was improved in collaboration with GO ontology developers and the SYSCILIA Consortium. These improvements to the GO terms for the functions and roles of ciliary proteins, along with the increase in annotations of the corresponding genes, enhance the representation of ciliary processes and localizations and improve access to these data during large-scale bioinformatic analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13630-018-0057-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-59074232018-04-30 Sensing the cilium, digital capture of ciliary data for comparative genomics investigations Christie, Karen R. Blake, Judith A. Cilia Research BACKGROUND: Cilia are specialized, hair-like structures that project from the cell bodies of eukaryotic cells. With increased understanding of the distribution and functions of various types of cilia, interest in these organelles is accelerating. To effectively use this great expansion in knowledge, this information must be made digitally accessible and available for large-scale analytical and computational investigation. Capture and integration of knowledge about cilia into existing knowledge bases, thus providing the ability to improve comparative genomic data analysis, is the objective of this work. METHODS: We focused on the capture of information about cilia as studied in the laboratory mouse, a primary model of human biology. The workflow developed establishes a standard for capture of comparative functional data relevant to human biology. We established the 310 closest mouse orthologs of the 302 human genes defined in the SYSCILIA Gold Standard set of ciliary genes. For the mouse genes, we identified biomedical literature for curation and used Gene Ontology (GO) curation paradigms to provide functional annotations from these publications. RESULTS: Employing a methodology for comprehensive capture of experimental data about cilia genes in structured, digital form, we established a workflow for curation of experimental literature detailing molecular function and roles of cilia proteins starting with the mouse orthologs of the human SYSCILIA gene set. We worked closely with the GO Consortium ontology development editors and the SYSCILIA Consortium to improve the representation of ciliary biology within the GO. During the time frame of the ontology improvement project, we have fully curated 134 of these 310 mouse genes, resulting in an increase in the number of ciliary and other experimental annotations. CONCLUSIONS: We have improved the GO annotations available for mouse genes orthologous to the human genes in the SYSCILIA Consortium’s Gold Standard set. In addition, ciliary terminology in the GO itself was improved in collaboration with GO ontology developers and the SYSCILIA Consortium. These improvements to the GO terms for the functions and roles of ciliary proteins, along with the increase in annotations of the corresponding genes, enhance the representation of ciliary processes and localizations and improve access to these data during large-scale bioinformatic analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13630-018-0057-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-19 /pmc/articles/PMC5907423/ /pubmed/29713460 http://dx.doi.org/10.1186/s13630-018-0057-0 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
Christie, Karen R.
Blake, Judith A.
Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title_full Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title_fullStr Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title_full_unstemmed Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title_short Sensing the cilium, digital capture of ciliary data for comparative genomics investigations
title_sort sensing the cilium, digital capture of ciliary data for comparative genomics investigations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907423/
https://www.ncbi.nlm.nih.gov/pubmed/29713460
http://dx.doi.org/10.1186/s13630-018-0057-0
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