TY - JOUR
T1 - Modeling the global effect of the basic-leucine zipper transcription factor 1 (bZIP1) on nitrogen and light regulation in Arabidopsis
AU - Obertello, Mariana
AU - Krouk, Gabriel
AU - Katari, Manpreet S.
AU - Runko, Suzan J.
AU - Coruzzi, Gloria M.
N1 - Funding Information:
We thank Dennis Shasha and Dan Tranchina for helpful discussions. This work was supported by the following grants to G.C.: National Institutes of Health (NIH) NIGMS Grant GM032877, DOE Grant DEFG02-92ER20071, and National Science Foundation (NSF) Arabidopsis 2010 Genome Grant MCB-0929338. M.O. and M.K. were supported by NIH NIGMS Grant GM032877 and DOE FG02-92ER20071. G.K. was supported by a European-FP7-International Outgoing Fellowships (Marie Curie) (AtSYSTM-BIOL; PIOF-GA-2008-220157). S. R. was funded by New York University. The author responsible for distribution of Materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors is Gloria Coruzzi ([email protected]) 1Center for Genomics and Systems Biology, Department of Biology, New York University. 100 Washington Square East, 1009 Main Building, New York, NY 10003, USA. 2Institut de Biologie Intégrative des Plantes, UMR 5004, Biochimie et Physiologie Moléculaire des Plantes, Agro-M/CNRS/INRA/ SupAgro/UM2, Montpellier, France. 3Instituto de Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Vuelta de Obligado 2490 piso 2, C1428ADN Buenos Aires, Argentina.
PY - 2010/8/12
Y1 - 2010/8/12
N2 - Background: Nitrogen and light are two major regulators of plant metabolism and development. While genes involved in the control of each of these signals have begun to be identified, regulators that integrate gene responses to nitrogen and light signals have yet to be determined. Here, we evaluate the role of bZIP1, a transcription factor involved in light and nitrogen sensing, by exposing wild-type (WT) and bZIP1 T-DNA null mutant plants to a combinatorial space of nitrogen (N) and light (L) treatment conditions and performing transcriptome analysis. We use ANOVA analysis combined with clustering and Boolean modeling, to evaluate the role of bZIP1 in mediating L and N signaling genome-wide.Results: This transcriptome analysis demonstrates that a mutation in the bZIP1 gene can alter the L and/or N-regulation of several gene clusters. More surprisingly, the bZIP1 mutation can also trigger N and/or L regulation of genes that are not normally controlled by these signals in WT plants. This analysis also reveals that bZIP1 can, to a large extent, invert gene regulation (e.g., several genes induced by N in WT plants are repressed by N in the bZIP1 mutant).Conclusion: These findings demonstrate that the bZIP1 mutation triggers a genome-wide de-regulation in response to L and/or N signals that range from i) a reduction of the L signal effect, to ii) unlocking gene regulation in response to L and N combinations. This systems biology approach demonstrates that bZIP1 tunes L and N signaling relationships genome-wide, and can suppress regulatory mechanisms hypothesized to be needed at different developmental stages and/or environmental conditions.
AB - Background: Nitrogen and light are two major regulators of plant metabolism and development. While genes involved in the control of each of these signals have begun to be identified, regulators that integrate gene responses to nitrogen and light signals have yet to be determined. Here, we evaluate the role of bZIP1, a transcription factor involved in light and nitrogen sensing, by exposing wild-type (WT) and bZIP1 T-DNA null mutant plants to a combinatorial space of nitrogen (N) and light (L) treatment conditions and performing transcriptome analysis. We use ANOVA analysis combined with clustering and Boolean modeling, to evaluate the role of bZIP1 in mediating L and N signaling genome-wide.Results: This transcriptome analysis demonstrates that a mutation in the bZIP1 gene can alter the L and/or N-regulation of several gene clusters. More surprisingly, the bZIP1 mutation can also trigger N and/or L regulation of genes that are not normally controlled by these signals in WT plants. This analysis also reveals that bZIP1 can, to a large extent, invert gene regulation (e.g., several genes induced by N in WT plants are repressed by N in the bZIP1 mutant).Conclusion: These findings demonstrate that the bZIP1 mutation triggers a genome-wide de-regulation in response to L and/or N signals that range from i) a reduction of the L signal effect, to ii) unlocking gene regulation in response to L and N combinations. This systems biology approach demonstrates that bZIP1 tunes L and N signaling relationships genome-wide, and can suppress regulatory mechanisms hypothesized to be needed at different developmental stages and/or environmental conditions.
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U2 - 10.1186/1752-0509-4-111
DO - 10.1186/1752-0509-4-111
M3 - Article
C2 - 20704717
AN - SCOPUS:77955406540
SN - 1752-0509
VL - 4
JO - BMC Systems Biology
JF - BMC Systems Biology
M1 - 111
ER -