- Research article
- Open Access
Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana
© Chen et al; licensee BioMed Central Ltd. 2010
Received: 20 October 2009
Accepted: 7 March 2010
Published: 7 March 2010
DnaJ proteins participate in many metabolic pathways through dynamic interactions with various components of these processes. The role of three small chloroplast-targeted DnaJ proteins, AtJ8 (At1 g80920), AtJ11 (At4 g36040) and AtJ20 (At4 g13830), was investigated here using knock-out mutants of Arabidopsis thaliana. Photochemical efficiency, capacity of CO2 assimilation, stabilization of Photosystem (PS) II dimers and supercomplexes under high light illumination, energy distribution between PSI and PSII and phosphorylation of PSII-LHCII proteins, global gene expression profiles and oxidative stress responses of these DnaJ mutants were analyzed.
Knockout of one of these proteins caused a series of events including a decrease in photosynthetic efficiency, destabilization of PSII complexes and loss of control for balancing the redox reactions in chloroplasts. Data obtained with DNA microarray analysis demonstrated that the lack of one of these DnaJ proteins triggers a global stress response and therefore confers the plants greater tolerance to oxidative stress induced by high light or methyl viologen treatments. Expression of a set of genes encoding enzymes that detoxify reactive oxygen species (ROS) as well as a number of stress-related transcription factors behaved in the mutants at growth light similarly to that when wild-type (WT) plants were transferred to high light. Also a set of genes related to redox regulation were upregulated in the mutants. On the other hand, although the three DnaJ proteins reside in chloroplasts, the expression of most genes encoding thylakoid membrane proteins was not changed in the mutants.
It is proposed that the tolerance of the DnaJ protein knockout plants to oxidative stress occurs at the expense of the flexibility of photosynthetic reactions. Despite the fact that the effects of the individual protein knockout on the response of plants to high light treatment are quite similar, it is conceivable that both specific- and cross-talk functions exist between the three small chloroplast-targeted DnaJ proteins, AtJ8, AtJ11 and AtJ20.
Molecular chaperones participate in many important metabolic and survival reactions through dynamic interactions with various components of given processes. DnaJ proteins, also called J-domain proteins, function as molecular co-chaperones of Hsp70 and play an important role in protein folding, unfolding, and assembly under both normal and stress conditions as well as in cellular secretory pathways [1, 2]. They are divided into three categories according to their domain composition  and have been identified in a variety of cellular compartments including cytosol , mitochondria , endoplastic reticulum , and chloroplasts . Some of the DnaJ proteins also bind to the plasma membrane .
DnaJ proteins belong to a large family with several members: 22 in yeast , 41 in humans  and at least 89 in Arabidopsis . According to our database searches at least 26 DnaJ proteins of Arabidopsis are predicted to have a chloroplast targeting signal and only few of them have been characterized. Based on only a few published studies it seems that the chloroplast-targeted DnaJ proteins participate in protein folding, unfolding and assembly processes . Vitha et al. reported that ARC6, a chloroplast-targeted DnaJ-like protein localized to the plastid envelope membrane, participates in division of plastids probably by functioning in the assembly and/or stabilization of the plastid-dividing FtsZ ring in Arabidopsis . It has been found that ATJ11, a chloroplast stroma localized DnaJ protein, is ubiquitously expressed in all plant organs examined so far . DnaJ proteins found in the Arabidopsis chloroplast thylakoid proteome are likely to be important in thylakoid biogenesis . Indeed, in Chlamydomonas, one chloroplast-targeted DnaJ protein was demonstrated to function in biogenesis of the thylakoid membrane .
Three DnaJ proteins, namely At1 g80920, At4 g36040 and At4 g13830, or AtJ8, AtJ11 and AtJ20, are small chloroplast-targeted DnaJ proteins in Arabidopsis with predicted molecular masses of 18.3-, 17.8- and 23.4-kD, respectively. These three proteins belong to the simplest group of the DnaJ proteins (type III) characterised by only one specific domain, the J-domain . According to public microarray databases their gene expression patterns resemble each other . We previously found that AtJ8 gene is upregulated in darkness  similar to that of AtJ20 gene (Supplementary material in ). To get more insights into the function of these small DnaJ proteins, the T-DNA insertion knockout mutants for AtJ8, AtJ11 and AtJ20 proteins, hereafter referred to as j8, j11 and j20, respectively, were isolated and characterised. The results provide evidence that the AtJ8, AtJ11 and AtJ20 proteins participate in optimization of various reactions of photosynthesis, and conversely, their absence triggers a global stress response.
Characterization of DnaJ single mutants
Localization of the three DnaJ proteins
Capacity of CO2assimilation
Stabilization of PSII dimers and supercomplexes under high light illumination
Energy distribution between PSI and PSII and phosphorylation of the PSII-LHCII proteins
As to PSII core protein phosphorylation, under GL conditions the j8 and j11 mutants exhibited more P-CP43, P-D1 and P-D2 proteins as compared to WT while the j20 had less (Figure 5B). Under HL conditions (both 500 and 1000 μmol photons m-2 s-1) the j11 and j20 mutants had a clearly higher level of PSII core protein phosphorylation. A long-term HL illumination (1000 μmol photons m-2 s-1) experiment showed that fluctuations in phosphorylation of both the PSII core and LHCII proteins were characteristic for WT during acclimation to this HL condition. The j8 mutant showed similar fluctuations, though not as drastic as in WT (Figure 5C). The j11 and j20 mutants, however, differed from the WT and j8, showing clearly delayed and less obvious drop in the phosphorylation level of both the PSII core and LHCII proteins, which in WT and j8 occurred after 6 h illumination at HL whereas in j11 and j20, a less distinctive drop in phosphorylation was recorded after 12 - 24 h illumination at HL. Moreover in all DnaJ mutants, j8, j11 and j20, long HL illumination resulted in more drastic phosphorylation of the Cas protein (Figure 5C), a typical stress response of plants .
Gene expression profiles
More interestingly, the DnaJ mutants showed stress-related regulation of several genes even at GL conditions. Expression of a number of genes related to transcription, translation and cellular signaling and to enzymes participating in the control of reactive oxygen species (ROS) and in redox regulation resembled that observed in WT upon transfer to HL (Additional file 4). Nevertheless, the DnaJ mutants also showed unique gene expression patterns from those induced in WT by HL treatment, including upregulation of several distinct genes encoding transcription factors, heat shock proteins, DnaJ proteins as well as antioxidant and redox proteins, among others (Additional file 4). Additionally, by using the MapMan tool, it was found that changes in expression of several genes related to distinct regulation pathways were quite similar in the DnaJ mutants at GL conditions to those recorded in the HL-treated WT (Additional file 5). Several clustered genes related to different functions, including hormone metabolism, stress response, redox regulation, transcriptional regulation, and protein degradation, were visualized and the results show that almost the same numbers of genes were regulated by HL in WT or by the lack of one DnaJ protein, AtJ8, AtJ11 or AtJ20 at GL conditions (Additional file 6). Particularly, the genes related to ubiquitin and ubiquitin E3 presented a high correlation between the HL stress response in WT and the DnaJ protein knockout (Additional file 6).
Oxidative stress tolerance in the DnaJ mutants
To investigate the tolerance of the DnaJ mutants to oxidative stress, 50 μM methyl viologen (MV) was supplied to plants followed by illumination at 1000 μmol photons m-2 s-1 HL for 6 h, and the cellular ion leakage of whole plant rosettes was determined. Plants untreated with MV showed no differences in ion leakage between the DnaJ mutants and WT. In WT plants the MV treatment strongly enhanced ion leakage levels, whereas in the j11 and j20 mutant plants the ion leakage was only slightly increased, indicating that the mutants had better resistance to MV-induced oxidative stress (Figure 8C, Additional file 1). Although j8 exhibited similar levels of ion leakage as WT in MV treated plants, the oxidation level of leaf total proteins isolated from the mutant was less severe than that in WT after the HL treatment (Figure 8D). In general, the DnaJ mutants showed less oxidation of leaf total proteins, particularly the Rubisco protein, as a response to environmental light intensity changes as compared to WT (Figure 8D).
The DnaJ proteins assist the Hsp70 chaperone proteins, participating in protein folding, unfolding, and assembly processes [1, 2]. Such functions, based mainly on biochemical experiments, are still unproven for the chloroplast DnaJ proteins, and their physiological roles remain largely unknown. Here we particularly focused our study on the physiological role of the three small chloroplast-targeted DnaJ proteins, AtJ8, AtJ11 and AtJ20 which according to our database searches, only contain the J-domain (data not shown) and thus possibly have divergent functions from ordinary DnaJ proteins. Although we did not obtain comprehensive information about the localization of the three small DnaJ proteins in different cell compartments, the immunoblotting experiments with protein extracts from isolated chloroplasts clearly showed that the three DnaJ proteins are targeted to chloroplasts in Arabidopsis (Figure 2).
Small chloroplast-targeted DnaJ proteins participate in regulation of CO2fixation and in stabilization of PSII supercomplexes and dimers
Due to chloroplast location of the three small DnaJ proteins, we applied simultaneous measurements of the responses of leaf gas exchange to light and CO2 concentration [18, 19], which provided first evidence of limitation of the in vivo photosynthesis in all the three DnaJ mutants. Both the lower slopes of light response curves and lower CO2 fixation at light saturation in the mutants (particularly in j11 and j20) (Figure 3) imply limitations in electron transport required for RuBP regeneration, Rubisco activity, or metabolism of triose phosphates [18, 19]. The A-Ci curves confirmed that particularly the activity of Rubisco is compromised in the DnaJ mutants, especially in j8. Considering the general function of the DnaJ proteins as chaperone proteins , the reduced amount of Rubisco Activase in the mutants reported here, suggests that the three small chloroplast DnaJ proteins are involved in the folding, unfolding, or assembly processes of this enzyme and thus participate in regulation of Rubisco activity . It should be noted that the functional mechanisms between the DnaJ proteins AtJ8, AtJ11 and AtJ20 in regulation of CO2 fixation might be somewhat different because the j8 mutant differed in the response to ambient CO2 concentration while the j11 and j20 mutants showed lower response to light intensity, which suggests the involvement of photosynthetic light reactions in limitation of CO2 fixation. Somewhat lower photochemical efficiency of PSII, the Fv/Fm ratio, particularly in j11 and j20 mutants after the HL treatment refers to malfunction of PSII. Moreover, the HL treatments of WT and the DnaJ mutant plants suggested the involvement of AtJ11 and AtJ20 in stabilization of PSII supercomplexes and dimers.
The deduction that these small chloroplast-targeted DnaJ proteins are related to regulation of CO2 assimilation is also supported by the data from DNA microarray studies. Several genes related to the Calvin-Benson cycle showed big changes in expression in the DnaJ mutants as compared to WT (Additional file 4). Particularly the expression of Ribose 5-phosphate isomerase was significantly downregulated in the mutants under both GL and HL conditions, implying this downregulation as one of the reasons for, or a consequence of, the lower CO2 assimilation in the mutants. On the contrary, the expression of most genes related to thylakoid membrane proteins was not changed in the mutants, neither under GL nor under HL conditions as compared to WT (Additional file 4). The expression of only the FZL-like protein gene was significantly downregulated in j11 and j20 under GL and in all the three mutants under HL (Additional file 4), implying that the FZL-like protein might function in co-operation with the DnaJ proteins and control the aggregation/disaggregation of PSII complexes since the FZL-like protein regulates the organization of the thylakoid network in chloroplasts .
Knocking out one of the small chloroplast-targeted DnaJ proteins modifies the capacity for dynamic regulation of chloroplast redox reactions
Energy distribution between PSII and PSI is regulated by phosphorylation of the PSII-LHCII complexes , which in turn is strongly dependent on the redox state of electron transfer components in the thylakoid membrane as well as in the soluble stroma . Although the differences in PSII-LHCII protein phosphorylation between both the three DnaJ mutants and the different light intensities did not allow to draw any strict conclusions about energy distribution between PSII and PSI, it was clearly evident that more phosphorylated thylakoid proteins accumulated in the DnaJ mutants, particularly j11 and j20 during all different short-term illumination conditions (Figure 5B and 5C). This prompted us to analyse the thylakoid phosphoprotein profiles in the course of long-term HL illumination of both the WT and DnaJ mutant plants. Indeed, the changes in the phosphorylation pattern of thylakoid proteins revealed the capacity of the electron transfer chain to acclimate to changes in light conditions. WT clearly showed a strong phosphorylation of PSII core proteins immediately after exposure to HL, which also reflects a high reduction state of the plastoquinone (PQ) pool . Nevertheless, the dynamics of thylakoid functions allowed re-oxidation of the PQ pool in the course of HL illumination and already after 6 h this was reflected in lower phosphorylation level of the PSII core proteins D1, D2 and CP43. j8 mutant also had such a capacity to respond to the HL treatment. The j11 and j20 mutant plants showed clearly less capacity for acclimation of the thylakoid redox reactions to prolonged exposure to HL and kept the PSII core proteins strongly phosphorylated during the entire HL treatment, implying highly reduced PQ pool. Similarly, a more severe stress response of the mutants as compared to WT after prolonged HL treatment can be deduced from the strong phosphorylation of the Cas protein, reflecting highly reduced electron transfer chain in all mutants . Cas protein is a calcium-sensing receptor that was found to be located in the stroma thylakoids of chloroplasts and functions in stress responses and signaling pathways .
Knocking out any one of the small chloroplast-targeted DnaJ protein triggers a global stress response
As discussed above, the knocking out of any one of the three small chloroplast-targeted DnaJ proteins AtJ8, AtJ11 or AtJ20 causes many events in Arabidopsis, which are reminiscent of generally known stress responses in plants. The most typical response is the increased tolerance of the mutant plants to oxidative stress induced by HL and MV (Figure 8). It was recently reported that the DnaJ family proteins participate in H2O2-induced gene expression matrix in higher plants as well as in yeast and cyanobacteria . The results reported here likewise show that the DnaJ proteins are involved in ROS-induced stress responses in Arabidopsis. The gene expression profiles of the DnaJ mutants, even under GL conditions, are quite similar to those induced upon ROS-producing HL treatment in WT (Figure 6). Moreover, the transcripts of some specific antioxidant genes, like apx6, cat1, CSD3, gpx5, glutaredoxin-like, were found to be specifically upregulated only in the three small chloroplast-targeted DnaJ knockout mutants (Additional file 3 and 4). Such upregulation of ROS scavenging and antioxidant systems coincided with lower H2O2 content in the DnaJ mutants than in WT, both at GL and HL conditions (Figure 8). Many genes encoding intracellular redox regulators such as thioredoxins and glutaredoxins with strong impact on stress tolerance  were upregulated together with several receptor kinases and G-proteins in the DnaJ mutants (Additional file 5), implying redox regulation in the stress tolerance of the DnaJ mutants. Moreover, the expression of a number of genes encoding conventional transcription factors and many novel ones containing zinc-finger, MYB, NAC and AP2 domains, which are tightly correlated with stress responses , showed significant modifications in the DnaJ mutants even under GL conditions (Additional file 3 and 4). Many of their target genes are likely involved in protein modification and degradation processes, as can be deduced from the MapMan analysis (Additional file 5). These results strongly indicate that a global stress response has been triggered in the three DnaJ mutants even in the absence of external stress.
The comparison of the gene expression profiles of our DnaJ mutants with those of other mutants deposited in the public microarray database further supported the idea that the tolerance of the DnaJ mutants to oxidative stress induced by MV is due to the trigger of a global stress response in these mutants (Additional file 6 and 7). The expression of 70 genes co-downregulated in the three DnaJ mutants is quite similar to that observed for oxidative stress related mutants of Arabidopsis, oxt6 and over-tAPX mutants. Oxt6 displays more tolerance to oxidative stress  whereas over-tAPX is a transgenic line which overexpresses the thylakoid-bound ascorbate peroxidase . On the contrary, completely opposite regulation of the 70 genes was displayed by HSP90(RNAi-A3), a HSP90-reduced line of Arabidopsis showing enhanced sensitivity to high temperature and to pathogen attack , and by the CSN mutants . The most studied CSN function is the regulation of protein degradation and beyond this, the CSN also acts as a transcriptional regulator .
The functions of the three small chloroplast-targeted DnaJ proteins AtJ8, AtJ11 and AtJ20 seem to be, at least partially, redundant in Arabidopsis, yet it is evident that also specific functions exist for each protein. Knockout of the AtJ8 protein revealed less drastic influence on photosynthetic parameters than the knockout of either the AtJ11 or the AtJ20 protein. Because of the small sizes and the lack of client protein-interaction domains, the multiple, yet subtle, effects on photosynthesis performance induced by the knockout of any one of the small DnaJ proteins, AtJ8, AtJ11 or AtJ20, makes it hard to distinguish the individual roles of these DnaJ proteins in co-chaperone/chaperone cohort. Nevertheless, in general, these small chloroplast DnaJ proteins participate in optimization of CO2 fixation, in stabilization of PSII complexes and balancing the electron transfer reactions. It is conceivable that the tolerance of the DnaJ protein knockout plants to oxidative stress results from an unbalance of the redox reactions in chloroplasts, thereby modifying the chloroplast retrograde signaling mechanisms and inducing the up- or down-regulation of stress responsive genes in the nucleus [16, 31].
As a whole, it can be concluded that both specific- and cross-talk functions exist between the three small chloroplast-targeted DnaJ proteins, and the tolerance of the DnaJ protein knockout plants to oxidative stress occurs at the expense of the flexibility of photosynthetic reactions. Further studies with double and triple mutants are expected to provide stronger phenotypes and also to give deeper insights into the functions of the AtJ8, AtJ11 and AtJ20 proteins in chloroplasts.
Plant materials, growth conditions and high light treatments
Arabidopsis thaliana ecotype Columbia (Col-0) wild-type (WT) and homozygous T-DNA insertion mutants for chloroplast-targeted DnaJ proteins, At1 g80920, At4 g36040, and At4 g13830, (j8, j11 and j20, respectively) were used in the experiments. The mutant lines salk_024617, salk_015630, and salk_134365 for AtJ8, AtJ11 and AtJ20, respectively, were selected to screen the homozygotes by standard PCR protocols recommended by SIGnAL (SALK, USA). Other mutant lines for the AtJ11 and AtJ20 proteins were salk_052270 and salk_125167, respectively, the results of which are presented in the Supplemental materials. Plants were grown under standard control conditions as described previously . High light treatments (500 and 1000 μmol photons m-2 s-1) were given using the same light source and were started immediately after the diurnal dark period. Mature rosette leaves from 4 to 6 weeks old plants were used for experiments.
Chlorophyll and protein determinations
Chlorophyll was determined according to Inskeep & Bloom  and Porra et al.  from leaf discs and isolated thylakoids, respectively. The protein content was determined using a DC (detergent-compatible) protein assay kit (Bio-Rad, Hercules, CA).
Measurements of PSII photochemical efficiency, 77 K chlorophyll fluorescence spectra, and CO2assimilation
PSII photochemical efficiency was determined as a ratio of variable fluorescence (Fv) to maximal fluorescence (Fm) measured from intact leaves with a Hansatech Plant Efficiency Analyser (Hansatech, King's Lynn, UK) after a dark incubation of 30 min. 77 K chlorophyll fluorescence emission spectra were measured as described by Soitamo et al. . CO2 assimilation was determined using an open-gas portable photosynthesis system (LI-6400, LI-COR, Lincoln, Nebraska, USA) with artificial blue-red light emitting diodes (LED) source. The response of CO2 assimilation to photosynthetic photon flux density (PPFD) was carried out by varying the PPFD from 2000 μmol m-2 s-1 to zero in the presence of 400 μmol mol-1 of CO2. The response of CO2 assimilation to CO2 concentration was determined at 1000 μmol m-2 s-1 of PPFD. 10 to 15 plants were measured for both the light response curves and the CO2 response curves based on three independent biological repeats.
Preparation of antibodies against the three DnaJ proteins
The antibodies for AtJ8, AtJ11 and AtJ20 were made by Innovagen Company (Lund, Sweden). Two rabbits were immunized using a specific synthetic peptide for each protein: AtJ8 (111-134) (NH2-) CKNQMEGTEEFEPFDVYDEGLNGMN (-CONH2); AtJ11 (127-136) (NH2-) CSVYDRRMLRR (-CONH2); AtJ20 (145-158) (NH2-) CRQNRYDQEVVEEKS (-CONH2).
Isolation of intact chloroplasts, thylakoid membranes and total leaf protein extracts
Intact chloroplasts were isolated from mature Arabidopsis leaves using a two-step Percoll gradient as described previously  and the thylakoid membranes as described by Suorsa et al. . For the total leaf protein extraction, the leaf disks of equal size were cut from mature leaves and carefully homogenized in grinding buffer, composed of shock buffer (10 mM HEPES-KOH, pH 7.6, 5 mM sorbitol, 5 mM MgCl2 and 10 mM NaF) and solubilization buffer  (1:1, v:v).
Blue-native-PAGE, SDS-PAGE and immunoblotting
Proteins were separated by SDS-PAGE using 15% (w/v) acrylamide gels with 6 M urea . After electrophoresis, proteins were electroblotted to a polyvinylidene fluoride (PVDF) membrane (Millipore, Watford, Herts, UK), and subsequently blocked with 5% milk (for immunoblotting with AtJ8, AtJ11, AtJ20, D1, D2, CP43, CF1, NDH-H, Rubisco, and Rubisco Activase antibodies) or fatty acid free BSA (for immunobloting with Phosphothreonine (P-Thr) antibody and APXs and PRXs antibodies). P-Thr-specific antibody was purchased from New England Biolabs . APXs and PRXs antibodies were obtained as described previously . Other protein-specific antibodies were purchased from Research Genetics (D1 and D2), or were kindly provided by Dr Heather J. Kane (Rubisco and Rubisco Activase), Dr Roberto Barbato (CP43), Dr Torill Hundal (CF1), and Dr Gilles Peltier (NDH-H). Preparation of samples and detection of protein oxidation were performed according to the protocol of the OxyBlot protein oxidation detection kit (Intergen, Purchase, NY, USA). The protein amounts loaded in the gels were carefully controlled to fall into the linear range of the antibody response curves.
Blue-native-PAGE was performed as described previously by Rokka et al. . After electrophoresis, the gels were photographed and then shortly destained by methanol. The destained gels were used for immunoblotting with D1 and CP43 antibodies, respectively.
In vivo H2O2detection and ion leakage measurement
Accumulation of H2O2 in leaves was detected using DAB (diaminobenzidine; Sigma-Aldrich, USA) as described in Kangasjärvi et al. . The sensitivity of expanded 5-week old rosettes to Methyl viologen (MV)-induced photo-oxidative stress was determined by gently spraying the plants with 50 μM MV at the end of the dark period as described in Kangasjärvi et al. .
Global changes in gene expression were explored with spotted Arabidopsis 24 k oligonucleotide arrays (MWG Biotech; ArrayExpress database accession number A-ATMX-2, Ireland). Plant rosettes, 4-weeks old, of wild-type and the DnaJ mutants, j8, j11 and j20, were collected from GL and from HL conditions after illumination for 6 h following the diurnal dark period. Total RNA was isolated with TRIzol-reagent as described previously  and subsequently followed as described by Kangasjärvi et al. . The arrays were scanned with an Agilent scanner, and the spot intensities were quantified with ScanArray Express Microarray Analysis system 2.0 (PerkinElmer Life Sciences, USA). The data from three biological replicates were analysed with the R program and Bioconductor packages. Average expression for each line and treatment was calculated and only the genes whose expression showed more than two-fold changes (upregulated or downregulated) with the p-value less than 0.05 and the B-value more than 2.0 were used for making the heatmaps and Venn diagrams. The B-value is the log-odds that the gene is differentially expressed . The higher B-value means the higher probability of gene differential expression.
This work was financially supported by the "New star" Project of Zhejiang University, PR China and the Academy of Finland (Project No. 118637). We thank the Salk Institute Genomic Analysis Laboratory for providing the sequence-indexed Arabidopsis T-DNA insertion mutants.
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