Genomic Analysis of the Nitrate Response Using a Nitrate Reductase-Null Mutant of Arabidopsis

Author:

Wang Rongchen1,Tischner Rudolf1,Gutiérrez Rodrigo A.1,Hoffman Maren1,Xing Xiujuan1,Chen Mingsheng1,Coruzzi Gloria1,Crawford Nigel M.1

Affiliation:

1. Section of Cell and Developmental Biology, Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093–0116 (R.W., X.X., N.M.C.); Albrecht von Haller Institut für Pflanzenwissenschaften, University of Gottingen, 37073 Gottingen, Germany (R.T., M.H.); Department of Biology, New York University, New York, New York 10003 (R.A.G., G.C.); and Institute of Geneti

Abstract

Abstract A nitrate reductase (NR)-null mutant of Arabidopsis was constructed that had a deletion of the major NR gene NIA2 and an insertion in the NIA1 NR gene. This mutant had no detectable NR activity and could not use nitrate as the sole nitrogen source. Starch mobilization was not induced by nitrate in this mutant but was induced by ammonium, indicating that nitrate was not the signal for this process. Microarray analysis of gene expression revealed that 595 genes responded to nitrate (5 mm nitrate for 2 h) in both wild-type and mutant plants. This group of genes was overrepresented most significantly in the functional categories of energy, metabolism, and glycolysis and gluconeogenesis. Because the nitrate response of these genes was NR independent, nitrate and not a downstream metabolite served as the signal. The microarray analysis also revealed that shoots can be as responsive to nitrate as roots, yet there was substantial organ specificity to the nitrate response.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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