Cargando…
Bacterial protein meta-interactomes predict cross-species interactions and protein function
BACKGROUND: Protein-protein interactions (PPIs) can offer compelling evidence for protein function, especially when viewed in the context of proteome-wide interactomes. Bacteria have been popular subjects of interactome studies: more than six different bacterial species have been the subjects of com...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353844/ https://www.ncbi.nlm.nih.gov/pubmed/28298180 http://dx.doi.org/10.1186/s12859-017-1585-0 |
_version_ | 1782515214336393216 |
---|---|
author | Caufield, J. Harry Wimble, Christopher Shary, Semarjit Wuchty, Stefan Uetz, Peter |
author_facet | Caufield, J. Harry Wimble, Christopher Shary, Semarjit Wuchty, Stefan Uetz, Peter |
author_sort | Caufield, J. Harry |
collection | PubMed |
description | BACKGROUND: Protein-protein interactions (PPIs) can offer compelling evidence for protein function, especially when viewed in the context of proteome-wide interactomes. Bacteria have been popular subjects of interactome studies: more than six different bacterial species have been the subjects of comprehensive interactome studies while several more have had substantial segments of their proteomes screened for interactions. The protein interactomes of several bacterial species have been completed, including several from prominent human pathogens. The availability of interactome data has brought challenges, as these large data sets are difficult to compare across species, limiting their usefulness for broad studies of microbial genetics and evolution. RESULTS: In this study, we use more than 52,000 unique protein-protein interactions (PPIs) across 349 different bacterial species and strains to determine their conservation across data sets and taxonomic groups. When proteins are collapsed into orthologous groups (OGs) the resulting meta-interactome still includes more than 43,000 interactions, about 14,000 of which involve proteins of unknown function. While conserved interactions provide support for protein function in their respective species data, we found only 429 PPIs (~1% of the available data) conserved in two or more species, rendering any cross-species interactome comparison immediately useful. The meta-interactome serves as a model for predicting interactions, protein functions, and even full interactome sizes for species with limited to no experimentally observed PPI, including Bacillus subtilis and Salmonella enterica which are predicted to have up to 18,000 and 31,000 PPIs, respectively. CONCLUSIONS: In the course of this work, we have assembled cross-species interactome comparisons that will allow interactomics researchers to anticipate the structures of yet-unexplored microbial interactomes and to focus on well-conserved yet uncharacterized interactors for further study. Such conserved interactions should provide evidence for important but yet-uncharacterized aspects of bacterial physiology and may provide targets for anti-microbial therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1585-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5353844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53538442017-03-22 Bacterial protein meta-interactomes predict cross-species interactions and protein function Caufield, J. Harry Wimble, Christopher Shary, Semarjit Wuchty, Stefan Uetz, Peter BMC Bioinformatics Research Article BACKGROUND: Protein-protein interactions (PPIs) can offer compelling evidence for protein function, especially when viewed in the context of proteome-wide interactomes. Bacteria have been popular subjects of interactome studies: more than six different bacterial species have been the subjects of comprehensive interactome studies while several more have had substantial segments of their proteomes screened for interactions. The protein interactomes of several bacterial species have been completed, including several from prominent human pathogens. The availability of interactome data has brought challenges, as these large data sets are difficult to compare across species, limiting their usefulness for broad studies of microbial genetics and evolution. RESULTS: In this study, we use more than 52,000 unique protein-protein interactions (PPIs) across 349 different bacterial species and strains to determine their conservation across data sets and taxonomic groups. When proteins are collapsed into orthologous groups (OGs) the resulting meta-interactome still includes more than 43,000 interactions, about 14,000 of which involve proteins of unknown function. While conserved interactions provide support for protein function in their respective species data, we found only 429 PPIs (~1% of the available data) conserved in two or more species, rendering any cross-species interactome comparison immediately useful. The meta-interactome serves as a model for predicting interactions, protein functions, and even full interactome sizes for species with limited to no experimentally observed PPI, including Bacillus subtilis and Salmonella enterica which are predicted to have up to 18,000 and 31,000 PPIs, respectively. CONCLUSIONS: In the course of this work, we have assembled cross-species interactome comparisons that will allow interactomics researchers to anticipate the structures of yet-unexplored microbial interactomes and to focus on well-conserved yet uncharacterized interactors for further study. Such conserved interactions should provide evidence for important but yet-uncharacterized aspects of bacterial physiology and may provide targets for anti-microbial therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1585-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-16 /pmc/articles/PMC5353844/ /pubmed/28298180 http://dx.doi.org/10.1186/s12859-017-1585-0 Text en © The Author(s). 2017 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 Article Caufield, J. Harry Wimble, Christopher Shary, Semarjit Wuchty, Stefan Uetz, Peter Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title | Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title_full | Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title_fullStr | Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title_full_unstemmed | Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title_short | Bacterial protein meta-interactomes predict cross-species interactions and protein function |
title_sort | bacterial protein meta-interactomes predict cross-species interactions and protein function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353844/ https://www.ncbi.nlm.nih.gov/pubmed/28298180 http://dx.doi.org/10.1186/s12859-017-1585-0 |
work_keys_str_mv | AT caufieldjharry bacterialproteinmetainteractomespredictcrossspeciesinteractionsandproteinfunction AT wimblechristopher bacterialproteinmetainteractomespredictcrossspeciesinteractionsandproteinfunction AT sharysemarjit bacterialproteinmetainteractomespredictcrossspeciesinteractionsandproteinfunction AT wuchtystefan bacterialproteinmetainteractomespredictcrossspeciesinteractionsandproteinfunction AT uetzpeter bacterialproteinmetainteractomespredictcrossspeciesinteractionsandproteinfunction |