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Using Reactome to build an autophagy mechanism knowledgebase
The 21st century has revealed much about the fundamental cellular process of autophagy. Autophagy controls the catabolism and recycling of various cellular components both as a constitutive process and as a response to stress and foreign material invasion. There is considerable knowledge of the mole...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204961/ https://www.ncbi.nlm.nih.gov/pubmed/32486891 http://dx.doi.org/10.1080/15548627.2020.1761659 |
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author | Varusai, Thawfeek Mohamed Jupe, Steven Sevilla, Cristoffer Matthews, Lisa Gillespie, Marc Stein, Lincoln Wu, Guanming D’Eustachio, Peter Metzakopian, Emmanouil Hermjakob, Henning |
author_facet | Varusai, Thawfeek Mohamed Jupe, Steven Sevilla, Cristoffer Matthews, Lisa Gillespie, Marc Stein, Lincoln Wu, Guanming D’Eustachio, Peter Metzakopian, Emmanouil Hermjakob, Henning |
author_sort | Varusai, Thawfeek Mohamed |
collection | PubMed |
description | The 21st century has revealed much about the fundamental cellular process of autophagy. Autophagy controls the catabolism and recycling of various cellular components both as a constitutive process and as a response to stress and foreign material invasion. There is considerable knowledge of the molecular mechanisms of autophagy, and this is still growing as new modalities emerge. There is a need to investigate autophagy mechanisms reliably, comprehensively and conveniently. Reactome is a freely available knowledgebase that consists of manually curated molecular events (reactions) organized into cellular pathways (https://reactome.org/). Pathways/reactions in Reactome are hierarchically structured, graphically presented and extensively annotated. Data analysis tools, such as pathway enrichment, expression data overlay and species comparison, are also available. For customized analysis, information can also be programmatically queried. Here, we discuss the curation and annotation of the molecular mechanisms of autophagy in Reactome. We also demonstrate the value that Reactome adds to research by reanalyzing a previously published work on genome-wide CRISPR screening of autophagy components. Abbreviations: CMA: chaperone-mediated autophagy; GO: Gene Ontology; MA: macroautophagy; MI: microautophagy; MTOR: mechanistic target of rapamycin kinase; SQSTM1: sequestosome 1 |
format | Online Article Text |
id | pubmed-8204961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-82049612021-06-24 Using Reactome to build an autophagy mechanism knowledgebase Varusai, Thawfeek Mohamed Jupe, Steven Sevilla, Cristoffer Matthews, Lisa Gillespie, Marc Stein, Lincoln Wu, Guanming D’Eustachio, Peter Metzakopian, Emmanouil Hermjakob, Henning Autophagy Resource The 21st century has revealed much about the fundamental cellular process of autophagy. Autophagy controls the catabolism and recycling of various cellular components both as a constitutive process and as a response to stress and foreign material invasion. There is considerable knowledge of the molecular mechanisms of autophagy, and this is still growing as new modalities emerge. There is a need to investigate autophagy mechanisms reliably, comprehensively and conveniently. Reactome is a freely available knowledgebase that consists of manually curated molecular events (reactions) organized into cellular pathways (https://reactome.org/). Pathways/reactions in Reactome are hierarchically structured, graphically presented and extensively annotated. Data analysis tools, such as pathway enrichment, expression data overlay and species comparison, are also available. For customized analysis, information can also be programmatically queried. Here, we discuss the curation and annotation of the molecular mechanisms of autophagy in Reactome. We also demonstrate the value that Reactome adds to research by reanalyzing a previously published work on genome-wide CRISPR screening of autophagy components. Abbreviations: CMA: chaperone-mediated autophagy; GO: Gene Ontology; MA: macroautophagy; MI: microautophagy; MTOR: mechanistic target of rapamycin kinase; SQSTM1: sequestosome 1 Taylor & Francis 2020-06-02 /pmc/articles/PMC8204961/ /pubmed/32486891 http://dx.doi.org/10.1080/15548627.2020.1761659 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Resource Varusai, Thawfeek Mohamed Jupe, Steven Sevilla, Cristoffer Matthews, Lisa Gillespie, Marc Stein, Lincoln Wu, Guanming D’Eustachio, Peter Metzakopian, Emmanouil Hermjakob, Henning Using Reactome to build an autophagy mechanism knowledgebase |
title | Using Reactome to build an autophagy mechanism knowledgebase |
title_full | Using Reactome to build an autophagy mechanism knowledgebase |
title_fullStr | Using Reactome to build an autophagy mechanism knowledgebase |
title_full_unstemmed | Using Reactome to build an autophagy mechanism knowledgebase |
title_short | Using Reactome to build an autophagy mechanism knowledgebase |
title_sort | using reactome to build an autophagy mechanism knowledgebase |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204961/ https://www.ncbi.nlm.nih.gov/pubmed/32486891 http://dx.doi.org/10.1080/15548627.2020.1761659 |
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