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Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics

Changes in response of a biological pathway could be a consequence of either pathway rewiring, changed input, or a combination of both. Most pathway analysis methods are not designed for mechanistic rewiring such as regulatory element variations. This limits our understanding of biological pathway e...

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Autores principales: Cotton, Travis B., Nguyen, Hien H., Said, Joseph I., Ouyang, Zhengyu, Zhang, Jinfa, Song, Mingzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894439/
https://www.ncbi.nlm.nih.gov/pubmed/25921728
http://dx.doi.org/10.1038/srep09634
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author Cotton, Travis B.
Nguyen, Hien H.
Said, Joseph I.
Ouyang, Zhengyu
Zhang, Jinfa
Song, Mingzhou
author_facet Cotton, Travis B.
Nguyen, Hien H.
Said, Joseph I.
Ouyang, Zhengyu
Zhang, Jinfa
Song, Mingzhou
author_sort Cotton, Travis B.
collection PubMed
description Changes in response of a biological pathway could be a consequence of either pathway rewiring, changed input, or a combination of both. Most pathway analysis methods are not designed for mechanistic rewiring such as regulatory element variations. This limits our understanding of biological pathway evolution. Here we present a Q-method to discern whether changed pathway response is caused by mechanistic rewiring of pathways due to evolution. The main innovation is a cumulative pathway interaction heterogeneity statistic accounting for rewiring-specific effects on the rate of change of each molecular variable across conditions. The Q-method remarkably outperformed differential-correlation based approaches on data from diverse biological processes. Strikingly, it also worked well in differentiating rewired chaotic systems, whose dynamics are notoriously difficult to predict. Applying the Q-method on transcriptome data of four yeasts, we show that pathway interaction heterogeneity for known metabolic and signaling pathways is indeed a predictor of interspecies genetic rewiring due to unbalanced TATA box-containing genes among the yeasts. The demonstrated effectiveness of the Q-method paves the way to understanding network evolution at the resolution of functional biological pathways.
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spelling pubmed-48944392016-06-10 Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics Cotton, Travis B. Nguyen, Hien H. Said, Joseph I. Ouyang, Zhengyu Zhang, Jinfa Song, Mingzhou Sci Rep Article Changes in response of a biological pathway could be a consequence of either pathway rewiring, changed input, or a combination of both. Most pathway analysis methods are not designed for mechanistic rewiring such as regulatory element variations. This limits our understanding of biological pathway evolution. Here we present a Q-method to discern whether changed pathway response is caused by mechanistic rewiring of pathways due to evolution. The main innovation is a cumulative pathway interaction heterogeneity statistic accounting for rewiring-specific effects on the rate of change of each molecular variable across conditions. The Q-method remarkably outperformed differential-correlation based approaches on data from diverse biological processes. Strikingly, it also worked well in differentiating rewired chaotic systems, whose dynamics are notoriously difficult to predict. Applying the Q-method on transcriptome data of four yeasts, we show that pathway interaction heterogeneity for known metabolic and signaling pathways is indeed a predictor of interspecies genetic rewiring due to unbalanced TATA box-containing genes among the yeasts. The demonstrated effectiveness of the Q-method paves the way to understanding network evolution at the resolution of functional biological pathways. Nature Publishing Group 2015-04-28 /pmc/articles/PMC4894439/ /pubmed/25921728 http://dx.doi.org/10.1038/srep09634 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Cotton, Travis B.
Nguyen, Hien H.
Said, Joseph I.
Ouyang, Zhengyu
Zhang, Jinfa
Song, Mingzhou
Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title_full Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title_fullStr Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title_full_unstemmed Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title_short Discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
title_sort discerning mechanistically rewired biological pathways by cumulative interaction heterogeneity statistics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894439/
https://www.ncbi.nlm.nih.gov/pubmed/25921728
http://dx.doi.org/10.1038/srep09634
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