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J. Biol. Chem., Vol. 279, Issue 21, 22204-22208, May 21, 2004

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Progression and Specificity of Protein Oxidation in the Life Cycle of Arabidopsis thaliana^*

Elin Johansson, Olof Olsson, and Thomas Nyström

From the Department of Cell and Molecular Biology, Göteborg University, Box 462, 405 30 Göteborg, Sweden

Received for publication, March 9, 2004

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Protein carbonylation is an irreversible oxidative process leading to a loss of function of the modified proteins, and in a variety of model systems, including worms, flies, and mammals, carbonyl levels gradually increase with age. In contrast, we report here that in Arabidopsis thaliana an initial increase in protein oxidation during the first 20 days of the life cycle of the plant is followed by a drastic reduction in protein carbonyls prior to bolting and flower development. Protein carbonylation prior to the transition to flowering targets specific proteins such as Hsp70, ATP synthases, the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), and proteins involved in light harvesting/energy transfer and the C2 oxidative photosynthetic carbon cycle. The precipitous fall in protein carbonyl levels is due to the specific reduction in the levels of oxidized proteins rather than an overall loss of chlorophyll and Rubisco associated with the senescence syndrome. The results are discussed in light of contemporary theories of aging in animals.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Endogenously generated reactive oxygen species, produced by the electron transport chains, react with different macromolecules in the cell and cause oxidative damage. Such oxidative damage accumulates over time during the life cycle of many organisms and has been suggested to be one possible cause of aging (1, 2). Protein carbonylation is a widely used marker of protein oxidation, and sensitive methods for its detection have been developed by Stadtman and Levine (3). Direct oxidative attack on Lys, Arg, Pro, and Thr or by secondary reactions via reactive carbohydrates and lipids on Cys, His, and Lys residues can lead to the formation of protein carbonyl derivatives (4, 5). Carbonylation of proteins inhibits or alters the activities of the proteins and increases their susceptibility to proteolytic attack (5, 6). In rats, aged flies, and senescing yeast and bacteria, this oxidation has been shown to be specific and targets enzymes of the Krebs cycle and other proteins, including stress proteins, Hsp70 chaperones, and translation elongation factors (7–10). In contrast, little is known about the occurrence of and targets for protein oxidation during the life cycle of annual plants.

The annual model plant Arabidopsis thaliana has a life cycle from seed to seed of about 6 weeks under optimal growth conditions. After germination, the above ground portion of the Arabidopsis plant initially develops two cotyledons and later a compressed rosette of leaves. All structures originate from the apical shoot meristem (11, 12). Later the shoot apical meristem will undergo a transition to an inflorescence meristem. Under long day conditions this occurs when the plant has six to ten leaves, although this varies with the genetic background and the environmental conditions. Somewhat later, after the main stem has elongated and produced a complex of higher order branches, a transition to a flower meristem occurs, from which the reproductive organs develop. After fertilization and as the seeds mature, the somatic tissues of the whole plant become increasingly senescent.

Leaf senescence is the final stage of leaf development that ultimately results in the death of the plant (reviewed in Ref. 13). During this final stage, the leaf cells undergo a programmed cell death process, referred to as the senescence syndrome (14). The most widely used biomarker for the senescence syndrome is the loss of chlorophyll associated with the degeneration of chloroplast internal structures (15). Leaf senescence is an intrinsic age-dependent process and its onset appears to be regulated by the age of individual leaves (16).

We demonstrate here that the quantitative and qualitative pattern of carbonylation during progression through the life cycle of the plant A. thaliana is distinct from that of the yeast, fly, nematode, and mammalian model systems. Carbonylation first increases with the age of the plant, similar to animals and microbes, but drops abruptly prior to the vegetative to reproductive transition and does not coincide with leaf senescence. Proteomic identification of the major targets for protein carbonylation in the plant leaves indicates that proteins directly and indirectly linked to chloroplast activities exhibit special problems with respect to oxidative damage. The data highlight that there is no inevitable, stochastic, increase in protein oxidation in aging tissues of the plant A. thaliana.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Culturing Conditions—Wild-type A. thaliana plants (ecotype Col-0) were grown on a mixture of 2:1:1 of soil:vermiculite:perlite in a greenhouse in a day/night temperature regime of 22/18 °C, an 18-h photoperiod, a photon flux density of 125 µmol m^-2 s^-1, and a relative humidity of 70%. Plants were watered twice a week with a nutrition solution as described (17).

Isolation of Cellular Proteins—Protein extractions and chlorophyll measurements were from leaf number 5 and 6, unless the extractions were from very young plants in which case the whole seedlings were used. Rosette leaves from different life stages were grinded in liquid N₂ using a precooled mortar and pestle. The powder was resuspended in a buffer containing 250 mM Tris-Cl, pH 8.5, 0.5 mM EDTA, 2% lithium dodecyl sulfate, 10% glycerol, and 2 mM pefabloc (protease inhibitor, Roche Applied Science). The sample was heated for 5 min at 75 °C. Tubes were cooled and centrifuged at 20,000 x g at 4 °C for 10 min. The supernatant was transferred to a fresh tube and the protein was acetone-extracted by addition of acetone to a final concentration of 80% (v/v) at -20 °C for 30 min and then centrifuged for 20,000 x g for 5 min at room temperature. After centrifugation and vacuum drying, the protein pellet was resuspended in the same buffer as above and stored at -20 °C after the protein concentration had been determined. The concentration of proteins was estimated using Pierce BCA protein quantification kit according to the manufacturer's instructions. The relative abundance of Rubisco¹ was determined using specific antibodies (from Agrisera, Vännäs, Sweden) and Western blotting. As a secondary antibody, anti-chicken IgG from Sigma (product number A9046) was used.

Carbonylation Assays—Detection of carbonylated proteins was performed using the chemical and immunological reagents of the OxyBlot^TM Oxidized Protein Detection Kit (Intergen). The carbonyl groups in the protein side chains were derivatized to 2,4-dinitrophenylhydrazone (DNP) by reaction with 2,4-dinitrophenylhydrazine (DNPH). The chemiluminescence blotting substrate (ECLplus) was obtained from Amersham Biosciences and used according to instructions provided by the manufacturer. Immobilon-P polyvinylidene diflouride membrane was from Millipore Corp. As described above, crude protein extracts were obtained during the different life stages of the plant, the extracts were reacted with the carbonyl reagent, DNPH, dot-blotted onto polyvinylidene diflouride membranes, and oxidatively modified proteins were detected with anti-DNP antibodies. In general, 5 µg of protein were loaded into the slot-blot apparatus and 50 µg onto two-dimensional gels.

Isolation of Mitochondria—All steps included in mitochondrial isolations were performed at 4 °C. Leaves (or whole seedlings) were harvested and immediately prepared. 5–10 g w/w was homogenized in 50 ml of grinding medium (0.3 M sucrose, 25 mM tetrasodium pyrophosphate, 2 mM EDTA, 10 mM KH₂PO₄, 1% polyvinylpyrrolidone-40, 1% bovine serum albumin, and 20 mM ascorbic acid, pH 7.2) using a chilled mortar and pestle. The homogenate was filtered through a single layer of damp, chilled, fine filter cloth and centrifuged at 4500 rpm (Beckmann JA-21 centrifuge, JA-20 rotor, 3000 x g) at 4 °C for 5 min. Supernatants were kept and centrifuged for 20 min at 12,000 rpm (17,000 x g). Pellets were collected and resuspended in a small volume of wash buffer (0.15 M sucrose, 10 mM TES, and 0.05% bovine serum albumin, pH 7.2) using a soft, small brush. The solution was combined into two tubes, which were filled up with wash buffer, and two centrifugation steps, as described above, were performed. Pellets containing the mitochondria were resuspended in a small volume of wash buffer and layered on top of a step Percoll gradient (gradient solution consisting of 0.75 M sucrose, 25 mM MOPS, 2.5 mM EDTA, and 0.5% bovine serum albumin, pH 7.2) at 21, 29, and 60%. The gradient was centrifuged for 40 min at 18 000 rpm (40,000 x g). The interface of the heaviest and the middle gradient densities contained the mitochondria. The band was collected by aspiration with a 1-ml pipetteman and diluted with wash buffer in a chilled 15-ml corex tube. This tube was centrifuged for 15 min at 15,000 rpm (27,000 x g). Pellets were resuspended in wash buffer and centrifuged once as described above. The pellet containing the purified mitochondria was resuspended in a small volume of wash buffer. The protein content was quantified after acetone precipitation.

Two-dimensional Gel Electrophoresis—Protein extracts were prepared and run on two-dimensional polyacrylamide gels by the methods of O'Farrell (18) with modifications (7). Ampholines with a pH range of 3.5–10 from Amersham Biosciences AB were used. Gel electrophoresis was carried out using 11.5% SDS-polyacrylamide gels, and the gels were either stained with Coomassie Blue or immunoblotted according to standard procedures. Signal intensities in gels and blots were analyzed by the computer program PDQuest (Bio-Rad). This program detects the chemiluminescence signal contributed by each separate protein spot and divides it by the total chemiluminescence signal of the whole blot. The program also detects the intensity of the Coomassie spot contributed by each protein spot and divides it with the intensity of the total Coomassie intensity of the whole gel. By making a ratio of these parameters a relative measurement of carbonylation/amount of protein can be calculated (the oxidation index).

Mass Spectrometry—Matrix-assisted laser desorption ionization time-of-flight data were acquired on an M@LDI-LR (Micromass, Manchester, UK) in reflectron mode and ESI data in mass spectrometry and mass spectrometry-mass spectrometry mode on a Q-Tof Ultima (Micromass, Manchester, UK). Protein identifications were done using MASCOT (available at www.matrixscience.com). Proteins were identified against the nr protein data base at NCBI, where a score of 74 corresponds to a 95% confidence level. All proteins were identified with scores above 95.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Protein Oxidation Is Age-dependent—A. thaliana plants (ecotype Col-0) were grown in a photoperiod of 18 h of light and 6 h of darkness, and protein extractions were made from different life cycle stages, ranging from before bolting to 25% leaf senescence. As shown in Fig. 1, A and B, protein carbonyl levels per total protein first increases as the rosette leaves becomes chronologically older. However, this increase is followed by an abrupt decrease in oxidation levels around 20 days after planting. The carbonylation levels in the last stages of the life cycle of the plant did not change (not shown). To evaluate whether there was any difference in carbonylation status during the photoperiod (day) and the period of active mitochondrial respiration (night), total cellular protein was extracted from plants, either 4 h after the light was switched on or 5 h after the light was switched off. The carbonyl signal from these two conditions was quantified and demonstrated the same trend in terms of the kinetics of protein oxidation during the plant life cycle (Fig. 1B). The growth conditions used resulted in bolting between 23 and 26 days after planting. In parallel to carbonylation measurements, chlorophyll content was analyzed, which demonstrated that the drastic drop in protein carbonyl levels occurred prior to the loss of chlorophyll that occurs during leaf senescence. (Fig. 1, B and C).

View larger version (24K): [in this window] [in a new window]   FIG. 1. A, schematic drawings of Arabidopsis plants during its progression through the lifecycle. B, kinetics of protein carbonyl levels in the leaves of differently aged plants. Open symbols represent samples obtained from the photoperiod, and black symbols represent samples obtained from the dark period. C, chlorophyll concentration and the Rubisco levels during plant development. Open symbols represent the chlorophyll concentration, and black symbols represent Rubisco levels. All experiments were repeated at least three times. Representative results are shown.

View larger version (49K): [in this window] [in a new window]   FIG. 2. A, representative blot of a two-dimensional gel, which has been incubated with anti-DNP antibodies for detection of carbonylated proteins. The corresponding Coomassie spots were cut out and subjected to mass spectrometry. B, oxidation index of the proteins isolated in Fig 2A. This is a measure of carbonylation signal/total amount of protein, calculated by the computer program PDQuest as described under "Experimental Procedures."

Carbonylation of Mitochondrial Proteins Is Specific—The relative abundance of some carbonylated proteins of the chloroplasts makes it difficult to detect carbonyl signals from other radical oxygen species-generating organelles, such as the mitochondria, in the crude cell extracts. Thus, to identify the most carbonylated proteins in the mitochondria, we isolated pure mitochondria from plants after 21 days of growth and applied immunochemical proteomics as described above. We found that the major targets for carbonylation in the mitochondria are glycine dehydrogenase (glycine cleavage system P-protein), a P-protein-like protein, the -subunit of the ATP synthase, a glycine hydroxymethyltransferase-like protein, and aminomethyltransferase (glycine cleavage system T-protein) (Table II). Like in chloroplasts, some very abundant mitochondrial proteins, e.g. the mitochondrial F₁ ATP synthase -subunit, citrate synthase, and malate dehydrogenase, did not show any signs of carbonylation suggesting that carbonylation sensitivity is specific also in this organelle.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Rubisco catalyzes the first step in net photosynthetic CO₂ assimilation and photorespiratory carbon oxidation. The active site of Rubisco assumes a closed conformation with certain phosphorylated ligands, and in the absence of catalysis, conversion of Rubisco from the closed to the open conformation is extremely slow. Rubisco-activase facilitates this process by releasing the inhibitory sugar phosphates (reviwed in Refs. 21 and 22). Rubisco-activase is an ATP-dependent AAA+ protein (ATPases associated with a variety of cellular activities), which includes a variety of proteins with chaperone-like functions (23). Interestingly, Rubisco-activase is present in two isoforms (24), differing only at the carboxyl terminus, which arise by alternative splicing of the gene transcript (25). The longer form is subjected to redox regulation via thioredoxin-f-mediated reduction of a pair of cysteine residues in the COOH-terminal extension (26). Based on pI, molecular mass, abundance, and mass spectrometry data, we concluded that both forms of the activase are carbonylated, but the longer form (activase I; Fig. 2A) is significantly more oxidized. This is also supported by the oxidation index calculated by the computer program PDQuest (Fig. 2B).

The OEC33 protein, together with OEC24 and OEC18, bind to the core of photosystem II at the lumenal surface to regulate the water oxidation process. Photosystem II is susceptible to damage caused by excess light, and the D1 protein of this system is a specific target for such photodamage. When damaged, D1 is rapidly degraded, and it has been suggested that OEC33 stimulates this degradation (27). It would be interesting to elucidate whether the carbonylation of OEC33 affects D1 proteolysis and whether oxidation of OEC33 is, itself, a direct consequence of photodamage.

Light-harvesting chlorophyll a/b-binding (Lhc) proteins are associated with the photosystems where they absorb energy through chlorophyll excitation and transfer the energy to photochemical reaction centers. In the case of higher plants, several reports have shown that the mRNA levels of cab transcripts fluctuate diurnally (reviewed in Ref. 28) with cab mRNA levels peaking in the late morning and reaching a minimum in the late evening. Interestingly, the carbonylation of this protein also fluctuated such that oxidation was mainly observed during the night (Table I).

All of the proteins identified as carbonylated from the mitochondrial fraction (except for the -subunit of the ATP synthase) play roles in the C₂ oxidative photosynthetic carbon cycle. Besides its carboxylse activity Rubisco has oxygenase activity, and therefore some ribulose-bisphosphate is converted to 2-phosphoglycolate, a compound that cannot be utilized by the Calvin cycle. 2-Phosphoglycolate is therefore salvaged by the C₂ oxidative photosynthetic carbon cycle. In this process, two molecules of glyoxylate are joined to form glycine. Glycine moves into the mitochondrion and becomes oxidatively decarboxylated by the glycine decarboxylase complex. As shown here, several components of this complex are modified by carbonylation. This is in line with the data of Taylor et al. (29) demonstrating that glycine decarboxylase activities in peas are exquisitely sensitive to oxidative stress.

The "stochastic" as opposed to "programmed" view of aging states that aging results from random deleterious events, and oxidative damage has been suggested to be a major contributor to such stochastic degeneration of cells and organisms. It has been demonstrated that the levels of carbonylated proteins increase with age in a large variety of species, including mammals, nematodes, and flies, and that such oxidative modification plays havoc with the catalytic activity and structural integrity of the target proteins (2, 3, 6, 7). The hypothesis is supported by experimental data demonstrating that the life span of fruitflies, for example, can be prolonged by overproducing antioxidants and that alleles that retard aging in yeast, flies, worms, and mice often boost the defense of the organism against oxidative damage (30, 31)

In plants, the concept of an individual, and therefore aging, is ambiguous. Nevertheless, the mechanisms that determine the life span of whole plants are obviously amenable to scientific examination and hypotheses aimed to explain plant longevity states that plant aging may be linked to resource allocation and competition between old and young tissues (e.g. Ref. 32). Specifically, it has been argued that older leaves are outcompeted by young tissues for "anti-aging" hormones (33), such as cytokinins (34). A variation on this theme is that young tissues seek to satisfy their demand for resources by exporting "death hormones" to older cells/tissues (35), and ethylene exhibits some characteristics of such hypothetical senescencepromoting substances (36). These theories are, in part, analogous to some evolutionary models of senescence in animals, which propose that there is a trade-off, or antagonism, between reproduction activities and cellular maintenance and repair (37, 38). As an inevitable consequence, an optimal life history entails an imperfect ability of the soma to resist intrinsic stress, such as oxidative damage.

With the above-mentioned theories in mind, we argued that old tissues, e.g. leaves, of an annual plant might loose their ability to defend themselves against intrinsically generated oxidative damage during transition to reproductive development. The results obtained did not support this notion. Instead, we found that old leaves rid themselves of oxidized proteins prior to bolting and flower development. At first glance, this suggests that the progression of oxidative damage in the life cycle of animals and plants is fundamentally different. Indeed, it clearly demonstrates that increased protein oxidation is not universally and inevitably related to the age of a biological tissue. However, one aspect of protein oxidation is similar in animals and plants, that is, production of offspring occurs at a time at which the overall oxidative damage in the organism is low. In animals this coincides with the early to middle stages of the life cycle of the organism, whereas in A. thaliana, it signifies the end point of its developmental progression. This begs the question of the physiological significance of the drastic drop in protein oxidation preceding flower development and to what extent this may affect the fitness of the offspring. In addition, it would be of interest to identify the temporal and molecular nature of the signals triggering the removal of damaged proteins and whether the elimination of such damage is a prerequisite for the transition to flowering.

	FOOTNOTES

 
^* This work was supported by a grant from the Swedish Natural Science Research Council (to T. N.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

To whom correspondence should be addressed: Dept. of Cell and Molecular Biology, Göteborg Univerity, Box 462, 40530 Göteborg, Sweden. Tel.: 46-31-7732582; Fax: 46-31-7732599; E-mail: Thomas.Nystrom{at}gmm.gu.se.

¹ The abbreviations used are: Rubisco, ribulose-1,5-bisphosphate carboxylase/oxygenase; DNP, 2,4-dinitrophenylhydrazone; DNPH, 2,4-dinitrophenylhydrazine; TES, 2-{[2-hydroxy-1,1-bis(hydroxymethyl)-ethyl]amino}ethanesulfonic acid; MOPS, 4-morpholinepropanesulfonic acid.

	ACKNOWLEDGMENTS

 
We thank Professor Elzbieta Glaser for all the help concerning isolation of mitochondria and Åsa Fredriksson for the artwork.

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TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 

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