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Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions
BACKGROUND: Plant secondary metabolites are critical to various biological processes. However, the regulations of these metabolites are complex because of regulatory rewiring or crosstalk. To unveil how regulatory behaviors on secondary metabolism reshape biological processes, we constructed and ana...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105546/ https://www.ncbi.nlm.nih.gov/pubmed/24993737 http://dx.doi.org/10.1186/1471-2229-14-180 |
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author | Lv, Qi Cheng, Rong Shi, Tieliu |
author_facet | Lv, Qi Cheng, Rong Shi, Tieliu |
author_sort | Lv, Qi |
collection | PubMed |
description | BACKGROUND: Plant secondary metabolites are critical to various biological processes. However, the regulations of these metabolites are complex because of regulatory rewiring or crosstalk. To unveil how regulatory behaviors on secondary metabolism reshape biological processes, we constructed and analyzed a dynamic regulatory network of secondary metabolic pathways in Arabidopsis. RESULTS: The dynamic regulatory network was constructed through integrating co-expressed gene pairs and regulatory interactions. Regulatory interactions were either predicted by conserved transcription factor binding sites (TFBSs) or proved by experiments. We found that integrating two data (co-expression and predicted regulatory interactions) enhanced the number of highly confident regulatory interactions by over 10% compared with using single data. The dynamic changes of regulatory network systematically manifested regulatory rewiring to explain the mechanism of regulation, such as in terpenoids metabolism, the regulatory crosstalk of RAV1 (AT1G13260) and ATHB1 (AT3G01470) on HMG1 (hydroxymethylglutaryl-CoA reductase, AT1G76490); and regulation of RAV1 on epoxysqualene biosynthesis and sterol biosynthesis. Besides, we investigated regulatory rewiring with expression, network topology and upstream signaling pathways. Regulatory rewiring was revealed by the variability of genes’ expression: pathway genes and transcription factors (TFs) were significantly differentially expressed under different conditions (such as terpenoids biosynthetic genes in tissue experiments and E2F/DP family members in genotype experiments). Both network topology and signaling pathways supported regulatory rewiring. For example, we discovered correlation among the numbers of pathway genes, TFs and network topology: one-gene pathways (such as δ-carotene biosynthesis) were regulated by a fewer TFs, and were not critical to metabolic network because of their low degrees in topology. Upstream signaling pathways of 50 TFs were identified to comprehend the underlying mechanism of TFs’ regulatory rewiring. CONCLUSION: Overall, this dynamic regulatory network largely improves the understanding of perplexed regulatory rewiring in secondary metabolism in Arabidopsis. |
format | Online Article Text |
id | pubmed-4105546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41055462014-07-23 Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions Lv, Qi Cheng, Rong Shi, Tieliu BMC Plant Biol Research Article BACKGROUND: Plant secondary metabolites are critical to various biological processes. However, the regulations of these metabolites are complex because of regulatory rewiring or crosstalk. To unveil how regulatory behaviors on secondary metabolism reshape biological processes, we constructed and analyzed a dynamic regulatory network of secondary metabolic pathways in Arabidopsis. RESULTS: The dynamic regulatory network was constructed through integrating co-expressed gene pairs and regulatory interactions. Regulatory interactions were either predicted by conserved transcription factor binding sites (TFBSs) or proved by experiments. We found that integrating two data (co-expression and predicted regulatory interactions) enhanced the number of highly confident regulatory interactions by over 10% compared with using single data. The dynamic changes of regulatory network systematically manifested regulatory rewiring to explain the mechanism of regulation, such as in terpenoids metabolism, the regulatory crosstalk of RAV1 (AT1G13260) and ATHB1 (AT3G01470) on HMG1 (hydroxymethylglutaryl-CoA reductase, AT1G76490); and regulation of RAV1 on epoxysqualene biosynthesis and sterol biosynthesis. Besides, we investigated regulatory rewiring with expression, network topology and upstream signaling pathways. Regulatory rewiring was revealed by the variability of genes’ expression: pathway genes and transcription factors (TFs) were significantly differentially expressed under different conditions (such as terpenoids biosynthetic genes in tissue experiments and E2F/DP family members in genotype experiments). Both network topology and signaling pathways supported regulatory rewiring. For example, we discovered correlation among the numbers of pathway genes, TFs and network topology: one-gene pathways (such as δ-carotene biosynthesis) were regulated by a fewer TFs, and were not critical to metabolic network because of their low degrees in topology. Upstream signaling pathways of 50 TFs were identified to comprehend the underlying mechanism of TFs’ regulatory rewiring. CONCLUSION: Overall, this dynamic regulatory network largely improves the understanding of perplexed regulatory rewiring in secondary metabolism in Arabidopsis. BioMed Central 2014-07-04 /pmc/articles/PMC4105546/ /pubmed/24993737 http://dx.doi.org/10.1186/1471-2229-14-180 Text en Copyright © 2014 Lv et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Lv, Qi Cheng, Rong Shi, Tieliu Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title | Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title_full | Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title_fullStr | Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title_full_unstemmed | Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title_short | Regulatory network rewiring for secondary metabolism in Arabidopsis thaliana under various conditions |
title_sort | regulatory network rewiring for secondary metabolism in arabidopsis thaliana under various conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105546/ https://www.ncbi.nlm.nih.gov/pubmed/24993737 http://dx.doi.org/10.1186/1471-2229-14-180 |
work_keys_str_mv | AT lvqi regulatorynetworkrewiringforsecondarymetabolisminarabidopsisthalianaundervariousconditions AT chengrong regulatorynetworkrewiringforsecondarymetabolisminarabidopsisthalianaundervariousconditions AT shitieliu regulatorynetworkrewiringforsecondarymetabolisminarabidopsisthalianaundervariousconditions |