A system biology approach highlights a hormonal enhancer effect on regulation of genes in a nitrate responsive "biomodule"

BMC Syst Biol. 2009 Jun 6:3:59. doi: 10.1186/1752-0509-3-59.

Abstract

Background: Nitrate-induced reprogramming of the transcriptome has recently been shown to be highly context dependent. Herein, a systems biology approach was developed to identify the components and role of cross-talk between nitrate and hormone signals, likely to be involved in the conditional response of NO3- signaling.

Results: Biclustering was used to identify a set of genes that are N-responsive across a range of Nitrogen (N)-treatment backgrounds (i.e. nitrogen treatments under different growth conditions) using a meta-dataset of 76 Affymetrix ATH1 chips from 5 different laboratories. Twenty-one biclusters were found to be N-responsive across subsets of this meta-dataset. N-bicluster 9 (126 genes) was selected for further analysis, as it was shown to be reproducibly responsive to NO3- as a signal, across a wide-variety of background conditions and datasets. N-bicluster 9 genes were then used as "seed" to identify putative cross-talk mechanisms between nitrate and hormone signaling. For this, the 126 nitrate-regulated genes in N-bicluster 9 were biclustered over a meta-dataset of 278 ATH1 chips spanning a variety of hormone treatments. This analysis divided the bicluster 9 genes into two classes: i) genes controlled by NO3- only vs. ii) genes controlled by both NO3- and hormones. The genes in the latter group showed a NO3- response that is significantly enhanced, compared to the former. In silico analysis identified two Cis-Regulatory Elements candidates (CRE) (E2F, HSE) potentially involved the interplay between NO3- and hormonal signals.

Conclusion: This systems analysis enabled us to derive a hypothesis in which hormone signals are proposed to enhance the nitrate response, providing a potential mechanistic explanation for the link between nitrate signaling and the control of plant development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Gene Expression Profiling
  • Gene Regulatory Networks / drug effects*
  • Genes, Plant / genetics
  • Hormones / pharmacology*
  • Multigene Family
  • Nitrates / pharmacology*
  • Plants / drug effects
  • Plants / genetics
  • Promoter Regions, Genetic / genetics
  • Regulatory Elements, Transcriptional / genetics
  • Reproducibility of Results
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Systems Biology*

Substances

  • Hormones
  • Nitrates