A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>

<p>Abstract</p> <p>Background</p> <p>Understanding gene function and genetic relationships is fundamental to our efforts to better understand biological systems. Previous studies systematically describing genetic interactions on a global scale have either focused on cor...

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Main Authors: Byrne Alexandra B, Weirauch Matthew T, Wong Victoria, Koeva Martina, Dixon Scott J, Stuart Joshua M, Roy Peter J
Format: Article
Language:English
Published: BMC 2007-09-01
Series:Journal of Biology
Online Access:http://jbiol.com/content/6/3/8
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spelling doaj-45df540364a34ca99fac8595531536892020-11-25T03:26:42ZengBMCJournal of Biology1478-58541475-49242007-09-0163810.1186/jbiol58A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>Byrne Alexandra BWeirauch Matthew TWong VictoriaKoeva MartinaDixon Scott JStuart Joshua MRoy Peter J<p>Abstract</p> <p>Background</p> <p>Understanding gene function and genetic relationships is fundamental to our efforts to better understand biological systems. Previous studies systematically describing genetic interactions on a global scale have either focused on core biological processes in protozoans or surveyed catastrophic interactions in metazoans. Here, we describe a reliable high-throughput approach capable of revealing both weak and strong genetic interactions in the nematode <it>Caenorhabditis elegans</it>.</p> <p>Results</p> <p>We investigated interactions between 11 'query' mutants in conserved signal transduction pathways and hundreds of 'target' genes compromised by RNA interference (RNAi). Mutant-RNAi combinations that grew more slowly than controls were identified, and genetic interactions inferred through an unbiased global analysis of the interaction matrix. A network of 1,246 interactions was uncovered, establishing the largest metazoan genetic-interaction network to date. We refer to this approach as systematic genetic interaction analysis (SGI). To investigate how genetic interactions connect genes on a global scale, we superimposed the SGI network on existing networks of physical, genetic, phenotypic and coexpression interactions. We identified 56 putative functional modules within the superimposed network, one of which regulates fat accumulation and is coordinated by interactions with <it>bar-1</it>(<it>ga80</it>), which encodes a homolog of β-catenin. We also discovered that SGI interactions link distinct subnetworks on a global scale. Finally, we showed that the properties of genetic networks are conserved between <it>C. elegans </it>and <it>Saccharomyces cerevisiae</it>, but that the connectivity of interactions within the current networks is not.</p> <p>Conclusions</p> <p>Synthetic genetic interactions may reveal redundancy among functional modules on a global scale, which is a previously unappreciated level of organization within metazoan systems. Although the buffering between functional modules may differ between species, studying these differences may provide insight into the evolution of divergent form and function.</p> http://jbiol.com/content/6/3/8
collection DOAJ
language English
format Article
sources DOAJ
author Byrne Alexandra B
Weirauch Matthew T
Wong Victoria
Koeva Martina
Dixon Scott J
Stuart Joshua M
Roy Peter J
spellingShingle Byrne Alexandra B
Weirauch Matthew T
Wong Victoria
Koeva Martina
Dixon Scott J
Stuart Joshua M
Roy Peter J
A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
Journal of Biology
author_facet Byrne Alexandra B
Weirauch Matthew T
Wong Victoria
Koeva Martina
Dixon Scott J
Stuart Joshua M
Roy Peter J
author_sort Byrne Alexandra B
title A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
title_short A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
title_full A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
title_fullStr A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
title_full_unstemmed A global analysis of genetic interactions in <it>Caenorhabditis elegans</it>
title_sort global analysis of genetic interactions in <it>caenorhabditis elegans</it>
publisher BMC
series Journal of Biology
issn 1478-5854
1475-4924
publishDate 2007-09-01
description <p>Abstract</p> <p>Background</p> <p>Understanding gene function and genetic relationships is fundamental to our efforts to better understand biological systems. Previous studies systematically describing genetic interactions on a global scale have either focused on core biological processes in protozoans or surveyed catastrophic interactions in metazoans. Here, we describe a reliable high-throughput approach capable of revealing both weak and strong genetic interactions in the nematode <it>Caenorhabditis elegans</it>.</p> <p>Results</p> <p>We investigated interactions between 11 'query' mutants in conserved signal transduction pathways and hundreds of 'target' genes compromised by RNA interference (RNAi). Mutant-RNAi combinations that grew more slowly than controls were identified, and genetic interactions inferred through an unbiased global analysis of the interaction matrix. A network of 1,246 interactions was uncovered, establishing the largest metazoan genetic-interaction network to date. We refer to this approach as systematic genetic interaction analysis (SGI). To investigate how genetic interactions connect genes on a global scale, we superimposed the SGI network on existing networks of physical, genetic, phenotypic and coexpression interactions. We identified 56 putative functional modules within the superimposed network, one of which regulates fat accumulation and is coordinated by interactions with <it>bar-1</it>(<it>ga80</it>), which encodes a homolog of β-catenin. We also discovered that SGI interactions link distinct subnetworks on a global scale. Finally, we showed that the properties of genetic networks are conserved between <it>C. elegans </it>and <it>Saccharomyces cerevisiae</it>, but that the connectivity of interactions within the current networks is not.</p> <p>Conclusions</p> <p>Synthetic genetic interactions may reveal redundancy among functional modules on a global scale, which is a previously unappreciated level of organization within metazoan systems. Although the buffering between functional modules may differ between species, studying these differences may provide insight into the evolution of divergent form and function.</p>
url http://jbiol.com/content/6/3/8
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