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ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion
Analysis of rewired upstream subnetworks impacting downstream differential gene expression aids the delineation of evolving molecular mechanisms. Cumulative statistics based on conventional differential correlation are limited for subnetwork rewiring analysis since rewiring is not necessarily equiva...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482087/ https://www.ncbi.nlm.nih.gov/pubmed/25897127 http://dx.doi.org/10.1093/nar/gkv358 |
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author | Zhang, Yang Liu, Z. Lewis Song, Mingzhou |
author_facet | Zhang, Yang Liu, Z. Lewis Song, Mingzhou |
author_sort | Zhang, Yang |
collection | PubMed |
description | Analysis of rewired upstream subnetworks impacting downstream differential gene expression aids the delineation of evolving molecular mechanisms. Cumulative statistics based on conventional differential correlation are limited for subnetwork rewiring analysis since rewiring is not necessarily equivalent to change in correlation coefficients. Here we present a computational method ChiNet to quantify subnetwork rewiring by statistical heterogeneity that enables detection of potential genotype changes causing altered transcription regulation in evolving organisms. Given a differentially expressed downstream gene set, ChiNet backtracks a rewired upstream subnetwork from a super-network including gene interactions known to occur under various molecular contexts. We benchmarked ChiNet for its high accuracy in distinguishing rewired artificial subnetworks, in silico yeast transcription-metabolic subnetworks, and rewired transcription subnetworks for Candida albicans versus Saccharomyces cerevisiae, against two differential-correlation based subnetwork rewiring approaches. Then, using transcriptome data from tolerant S. cerevisiae strain NRRL Y-50049 and a wild-type intolerant strain, ChiNet identified 44 metabolic pathways affected by rewired transcription subnetworks anchored to major adaptively activated transcription factor genes YAP1, RPN4, SFP1 and ROX1, in response to toxic chemical challenges involved in lignocellulose-to-biofuels conversion. These findings support the use of ChiNet in rewiring analysis of subnetworks where differential interaction patterns resulting from divergent nonlinear dynamics abound. |
format | Online Article Text |
id | pubmed-4482087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44820872015-06-30 ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion Zhang, Yang Liu, Z. Lewis Song, Mingzhou Nucleic Acids Res Computational Biology Analysis of rewired upstream subnetworks impacting downstream differential gene expression aids the delineation of evolving molecular mechanisms. Cumulative statistics based on conventional differential correlation are limited for subnetwork rewiring analysis since rewiring is not necessarily equivalent to change in correlation coefficients. Here we present a computational method ChiNet to quantify subnetwork rewiring by statistical heterogeneity that enables detection of potential genotype changes causing altered transcription regulation in evolving organisms. Given a differentially expressed downstream gene set, ChiNet backtracks a rewired upstream subnetwork from a super-network including gene interactions known to occur under various molecular contexts. We benchmarked ChiNet for its high accuracy in distinguishing rewired artificial subnetworks, in silico yeast transcription-metabolic subnetworks, and rewired transcription subnetworks for Candida albicans versus Saccharomyces cerevisiae, against two differential-correlation based subnetwork rewiring approaches. Then, using transcriptome data from tolerant S. cerevisiae strain NRRL Y-50049 and a wild-type intolerant strain, ChiNet identified 44 metabolic pathways affected by rewired transcription subnetworks anchored to major adaptively activated transcription factor genes YAP1, RPN4, SFP1 and ROX1, in response to toxic chemical challenges involved in lignocellulose-to-biofuels conversion. These findings support the use of ChiNet in rewiring analysis of subnetworks where differential interaction patterns resulting from divergent nonlinear dynamics abound. Oxford University Press 2015-05-19 2015-04-20 /pmc/articles/PMC4482087/ /pubmed/25897127 http://dx.doi.org/10.1093/nar/gkv358 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 Zhang, Yang Liu, Z. Lewis Song, Mingzhou ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title | ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title_full | ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title_fullStr | ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title_full_unstemmed | ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title_short | ChiNet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
title_sort | chinet uncovers rewired transcription subnetworks in tolerant yeast for advanced biofuels conversion |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482087/ https://www.ncbi.nlm.nih.gov/pubmed/25897127 http://dx.doi.org/10.1093/nar/gkv358 |
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