A system biology approach highlights a hormonal enhancer effect on regulation of genes in a nitrate responsive "biomodule"
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作者:
Nero, Damion
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NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USANYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
Nero, Damion
[1
]
Krouk, Gabriel
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NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USANYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
Krouk, Gabriel
[1
]
Tranchina, Daniel
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NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
NYU, Courant Inst Math Sci, New York, NY 10012 USANYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
Tranchina, Daniel
[1
,2
]
Coruzzi, Gloria M.
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NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USANYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
Coruzzi, Gloria M.
[1
]
机构:
[1] NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
[2] NYU, Courant Inst Math Sci, New York, NY 10012 USA
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 ATHI 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 ATHI 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.
机构:
Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
Guo, FQ
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Wang, RC
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Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
Wang, RC
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Crawford, NM
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Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
机构:
Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
Guo, FQ
;
Wang, RC
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Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
Wang, RC
;
Crawford, NM
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机构:
Univ Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Sect Cell & Dev Biol, La Jolla, CA 92093 USA