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Learning from the unknown: exploring the range of bacterial functionality
Determining the repertoire of a microbe's molecular functions is a central question in microbial biology. Modern techniques achieve this goal by comparing microbial genetic material against reference databases of functionally annotated genes/proteins or known taxonomic markers such as 16S rRNA....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602916/ https://www.ncbi.nlm.nih.gov/pubmed/37739408 http://dx.doi.org/10.1093/nar/gkad757 |
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author | Mahlich, Yannick Zhu, Chengsheng Chung, Henri Velaga, Pavan K De Paolis Kaluza, M Clara Radivojac, Predrag Friedberg, Iddo Bromberg, Yana |
author_facet | Mahlich, Yannick Zhu, Chengsheng Chung, Henri Velaga, Pavan K De Paolis Kaluza, M Clara Radivojac, Predrag Friedberg, Iddo Bromberg, Yana |
author_sort | Mahlich, Yannick |
collection | PubMed |
description | Determining the repertoire of a microbe's molecular functions is a central question in microbial biology. Modern techniques achieve this goal by comparing microbial genetic material against reference databases of functionally annotated genes/proteins or known taxonomic markers such as 16S rRNA. Here, we describe a novel approach to exploring bacterial functional repertoires without reference databases. Our Fusion scheme establishes functional relationships between bacteria and assigns organisms to Fusion-taxa that differ from otherwise defined taxonomic clades. Three key findings of our work stand out. First, bacterial functional comparisons outperform marker genes in assigning taxonomic clades. Fusion profiles are also better for this task than other functional annotation schemes. Second, Fusion-taxa are robust to addition of novel organisms and are, arguably, able to capture the environment-driven bacterial diversity. Finally, our alignment-free nucleic acid-based Siamese Neural Network model, created using Fusion functions, enables finding shared functionality of very distant, possibly structurally different, microbial homologs. Our work can thus help annotate functional repertoires of bacterial organisms and further guide our understanding of microbial communities. |
format | Online Article Text |
id | pubmed-10602916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106029162023-10-28 Learning from the unknown: exploring the range of bacterial functionality Mahlich, Yannick Zhu, Chengsheng Chung, Henri Velaga, Pavan K De Paolis Kaluza, M Clara Radivojac, Predrag Friedberg, Iddo Bromberg, Yana Nucleic Acids Res Computational Biology Determining the repertoire of a microbe's molecular functions is a central question in microbial biology. Modern techniques achieve this goal by comparing microbial genetic material against reference databases of functionally annotated genes/proteins or known taxonomic markers such as 16S rRNA. Here, we describe a novel approach to exploring bacterial functional repertoires without reference databases. Our Fusion scheme establishes functional relationships between bacteria and assigns organisms to Fusion-taxa that differ from otherwise defined taxonomic clades. Three key findings of our work stand out. First, bacterial functional comparisons outperform marker genes in assigning taxonomic clades. Fusion profiles are also better for this task than other functional annotation schemes. Second, Fusion-taxa are robust to addition of novel organisms and are, arguably, able to capture the environment-driven bacterial diversity. Finally, our alignment-free nucleic acid-based Siamese Neural Network model, created using Fusion functions, enables finding shared functionality of very distant, possibly structurally different, microbial homologs. Our work can thus help annotate functional repertoires of bacterial organisms and further guide our understanding of microbial communities. Oxford University Press 2023-09-22 /pmc/articles/PMC10602916/ /pubmed/37739408 http://dx.doi.org/10.1093/nar/gkad757 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology Mahlich, Yannick Zhu, Chengsheng Chung, Henri Velaga, Pavan K De Paolis Kaluza, M Clara Radivojac, Predrag Friedberg, Iddo Bromberg, Yana Learning from the unknown: exploring the range of bacterial functionality |
title | Learning from the unknown: exploring the range of bacterial functionality |
title_full | Learning from the unknown: exploring the range of bacterial functionality |
title_fullStr | Learning from the unknown: exploring the range of bacterial functionality |
title_full_unstemmed | Learning from the unknown: exploring the range of bacterial functionality |
title_short | Learning from the unknown: exploring the range of bacterial functionality |
title_sort | learning from the unknown: exploring the range of bacterial functionality |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602916/ https://www.ncbi.nlm.nih.gov/pubmed/37739408 http://dx.doi.org/10.1093/nar/gkad757 |
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