Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation

Chloroplast biogenesis involves careful coordination of both plastid and nuclear gene expression, which is achieved in part by retrograde signaling from the chloroplast to the nucleus. This can be demonstrated by the fact that the herbicide, Norflurazon (NF), which causes bleaching of chloroplasts, prevents the light induction of photosynthesis-related genes in the nucleus. It has been proposed that the tetrapyrrole pathway intermediate Mg-protoporphyrin IX acts as the signaling molecule in this pathway and accumulates in the chloroplasts and cytosol of the cell after NF treatment. Here we present data that demonstrate that this model is too simplistic. We have developed a sensitive liquid chromatography-mass spectrometry (LC/MS) method to measure tetrapyrrole intermediates and have shown that no Mg-protoporphyrin IX, nor indeed any other chlorophyll-biosynthesis intermediate, can be detected in NF-treated plants under conditions in which nuclear gene expression is repressed. Conversely when endogenous Mg-protoporphyrin IX levels are artificially increased by supplementation with the tetrapyrrole precursor, 5-aminolevulinic acid, the expression of nuclear-encoded photosynthetic genes is induced, not repressed. We also demonstrate that NF-treatment leads to a strong down-regulation of tetrapyrrole biosynthesis genes, consistent with the absence of an accumulation of tetrapyrrole intermediates. Finally, there is no correlation between nuclear-gene expression and any of the chlorophyll biosynthetic intermediates over a range of growth conditions and treatments. Instead, it is possible that a perturbation of tetrapyrrole synthesis may lead to localized ROS production or an altered redox state of the plastid, which could mediate retrograde signaling.

[1]  Joanne Chory,et al.  Signals from Chloroplasts Converge to Regulate Nuclear Gene Expression , 2007, Science.

[2]  W. Rüdiger,et al.  The greening process in cress seedlings. V. Possible interference of chlorophyll precursors, accumulated after thujaplicin treatment, with light-regulated expression of Lhc genes , 1996 .

[3]  Alison G. Smith,et al.  Expression analysis of the two ferrochelatase genes in Arabidopsis in different tissues and under stress conditions reveals their different roles in haem biosynthesis , 2002, Plant Molecular Biology.

[4]  B. Grimm,et al.  Metabolic control of the tetrapyrrole biosynthetic pathway for porphyrin distribution in the barley mutant albostrians. , 2003, The Plant journal : for cell and molecular biology.

[5]  Daniel MacLean,et al.  Coordination of plastid and nuclear gene expression. , 2003, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[6]  E. López-Juez,et al.  Arabidopsis cue mutants with defective plastids are impaired primarily in the photocontrol of expression of photosynthesis-associated nuclear genes , 2005, Plant Molecular Biology.

[7]  Cornelia Göbel,et al.  Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.014662. , 2003, The Plant Cell Online.

[8]  M. J. Terry,et al.  Green or red: what stops the traffic in the tetrapyrrole pathway? , 2003, Trends in plant science.

[9]  R. Tanaka,et al.  Tetrapyrrole biosynthesis in higher plants. , 2007, Annual review of plant biology.

[10]  U. Olsson,et al.  Analysis of gun phenotype in barley magnesium chelatase and Mg-protoporphyrin IX monomethyl ester cyclase mutants. , 2005, Plant physiology and biochemistry : PPB.

[11]  H. Hirt,et al.  Reactive oxygen species: metabolism, oxidative stress, and signal transduction. , 2004, Annual review of plant biology.

[12]  J Chory,et al.  Interactions between hy1 and gun mutants of Arabidopsis, and their implications for plastid/nuclear signalling. , 2000, The Plant journal : for cell and molecular biology.

[13]  M. L. Ujwal,et al.  Divergent regulation of the HEMA gene family encoding glutamyl-tRNA reductase in Arabidopsis thaliana: expression of HEMA2 is regulated by sugars, but is independent of light and plastid signalling , 2002, Plant Molecular Biology.

[14]  H. Ohta,et al.  Induction of Isoforms of Tetrapyrrole Biosynthetic Enzymes, AtHEMA2 and AtFC1, under Stress Conditions and Their Physiological Functions in Arabidopsis12[W][OA] , 2007, Plant Physiology.

[15]  T. Sakurai,et al.  Identification of Arabidopsis Genes Regulated by High Light–Stress Using cDNA Microarray¶ , 2003, Photochemistry and photobiology.

[16]  E. Huq,et al.  PHYTOCHROME-INTERACTING FACTOR 1 Is a Critical bHLH Regulator of Chlorophyll Biosynthesis , 2004, Science.

[17]  J. Ecker,et al.  GUN4, a Regulator of Chlorophyll Synthesis and Intracellular Signaling , 2003, Science.

[18]  T. Pfannschmidt Chloroplast redox signals: how photosynthesis controls its own genes. , 2003, Trends in plant science.

[19]  M. J. Terry,et al.  The nuclear genes Lhcb and HEMA1 are differentially sensitive to plastid signals and suggest distinct roles for the GUN1 and GUN5 plastid-signalling pathways during de-etiolation. , 2004, The Plant journal : for cell and molecular biology.

[20]  J. Chory,et al.  Arabidopsis genomes uncoupled 5 (GUN5) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Joanne Chory,et al.  Plastid-to-nucleus retrograde signaling. , 2006, Annual review of plant biology.

[22]  Samuel I. Beale,et al.  Enzymes of chlorophyll biosynthesis , 1999, Photosynthesis Research.

[23]  Thierry Lagrange,et al.  Knock-out of the Magnesium Protoporphyrin IX Methyltransferase Gene in Arabidopsis , 2007, Journal of Biological Chemistry.

[24]  M. J. Terry,et al.  Loss of Nuclear Gene Expression during the Phytochrome A-Mediated Far-Red Block of Greening Response1 , 2002, Plant Physiology.

[25]  J. Papenbrock,et al.  Expression studies in tetrapyrrole biosynthesis: inverse maxima of magnesium chelatase and ferrochelatase activity during cyclic photoperiods , 1999, Planta.

[26]  B. Grimm,et al.  Recent advances in chlorophyll biosynthesis and breakdown in higher plants , 2004, Plant Molecular Biology.

[27]  N. La Rocca,et al.  Amitrole treatment of etiolated barley seedlings leads to deregulation of tetrapyrrole synthesis and to reduced expression of Lhc and RbcS genes , 2001, Planta.

[28]  T. Masuda,et al.  The steady-state level of Mg-protoporphyrin IX is not a determinant of plastid-to-nucleus signaling in Arabidopsis , 2008, Proceedings of the National Academy of Sciences.

[29]  M. J. Terry,et al.  Light-signalling pathways leading to the co-ordinated expression of HEMA1 and Lhcb during chloroplast development in Arabidopsis thaliana. , 2002, The Plant journal : for cell and molecular biology.

[30]  R. Oelmüller,et al.  Photooxidative destruction of chloroplasts and its consequences for expression of nuclear genes , 2004, Planta.

[31]  T. Mockler,et al.  Multiple Signals from Damaged Chloroplasts Converge on a Common Pathway to Regulate Nuclear Gene Expression , 2007 .

[32]  D. Söll,et al.  Regulation of HEMA1 expression by phytochrome and a plastid signal during de-etiolation in Arabidopsis thaliana. , 2001, The Plant journal : for cell and molecular biology.

[33]  Peter Kindgren,et al.  In Vivo Visualization of Mg-ProtoporphyrinIX, a Coordinator of Photosynthetic Gene Expression in the Nucleus and the Chloroplast[W] , 2007, The Plant Cell Online.

[34]  J. Ecker,et al.  Chloroplast to nucleus communication triggered by accumulation of Mg-protoporphyrinIX , 2003, Nature.