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Identifying mouse developmental essential genes using machine learning
The genes that are required for organismal survival are annotated as ‘essential genes’. Identifying all the essential genes of an animal species can reveal critical functions that are needed during the development of the organism. To inform studies on mouse development, we developed a supervised mac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307915/ https://www.ncbi.nlm.nih.gov/pubmed/30563825 http://dx.doi.org/10.1242/dmm.034546 |
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author | Tian, David Wenlock, Stephanie Kabir, Mitra Tzotzos, George Doig, Andrew J. Hentges, Kathryn E. |
author_facet | Tian, David Wenlock, Stephanie Kabir, Mitra Tzotzos, George Doig, Andrew J. Hentges, Kathryn E. |
author_sort | Tian, David |
collection | PubMed |
description | The genes that are required for organismal survival are annotated as ‘essential genes’. Identifying all the essential genes of an animal species can reveal critical functions that are needed during the development of the organism. To inform studies on mouse development, we developed a supervised machine learning classifier based on phenotype data from mouse knockout experiments. We used this classifier to predict the essentiality of mouse genes lacking experimental data. Validation of our predictions against a blind test set of recent mouse knockout experimental data indicated a high level of accuracy (>80%). We also validated our predictions for other mouse mutagenesis methodologies, demonstrating that the predictions are accurate for lethal phenotypes isolated in random chemical mutagenesis screens and embryonic stem cell screens. The biological functions that are enriched in essential and non-essential genes have been identified, showing that essential genes tend to encode intracellular proteins that interact with nucleic acids. The genome distribution of predicted essential and non-essential genes was analysed, demonstrating that the density of essential genes varies throughout the genome. A comparison with human essential and non-essential genes was performed, revealing conservation between human and mouse gene essentiality status. Our genome-wide predictions of mouse essential genes will be of value for the planning of mouse knockout experiments and phenotyping assays, for understanding the functional processes required during mouse development, and for the prioritisation of disease candidate genes identified in human genome and exome sequence datasets. |
format | Online Article Text |
id | pubmed-6307915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63079152018-12-28 Identifying mouse developmental essential genes using machine learning Tian, David Wenlock, Stephanie Kabir, Mitra Tzotzos, George Doig, Andrew J. Hentges, Kathryn E. Dis Model Mech Resource Article The genes that are required for organismal survival are annotated as ‘essential genes’. Identifying all the essential genes of an animal species can reveal critical functions that are needed during the development of the organism. To inform studies on mouse development, we developed a supervised machine learning classifier based on phenotype data from mouse knockout experiments. We used this classifier to predict the essentiality of mouse genes lacking experimental data. Validation of our predictions against a blind test set of recent mouse knockout experimental data indicated a high level of accuracy (>80%). We also validated our predictions for other mouse mutagenesis methodologies, demonstrating that the predictions are accurate for lethal phenotypes isolated in random chemical mutagenesis screens and embryonic stem cell screens. The biological functions that are enriched in essential and non-essential genes have been identified, showing that essential genes tend to encode intracellular proteins that interact with nucleic acids. The genome distribution of predicted essential and non-essential genes was analysed, demonstrating that the density of essential genes varies throughout the genome. A comparison with human essential and non-essential genes was performed, revealing conservation between human and mouse gene essentiality status. Our genome-wide predictions of mouse essential genes will be of value for the planning of mouse knockout experiments and phenotyping assays, for understanding the functional processes required during mouse development, and for the prioritisation of disease candidate genes identified in human genome and exome sequence datasets. The Company of Biologists Ltd 2018-12-01 2018-12-13 /pmc/articles/PMC6307915/ /pubmed/30563825 http://dx.doi.org/10.1242/dmm.034546 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Resource Article Tian, David Wenlock, Stephanie Kabir, Mitra Tzotzos, George Doig, Andrew J. Hentges, Kathryn E. Identifying mouse developmental essential genes using machine learning |
title | Identifying mouse developmental essential genes using machine learning |
title_full | Identifying mouse developmental essential genes using machine learning |
title_fullStr | Identifying mouse developmental essential genes using machine learning |
title_full_unstemmed | Identifying mouse developmental essential genes using machine learning |
title_short | Identifying mouse developmental essential genes using machine learning |
title_sort | identifying mouse developmental essential genes using machine learning |
topic | Resource Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307915/ https://www.ncbi.nlm.nih.gov/pubmed/30563825 http://dx.doi.org/10.1242/dmm.034546 |
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