Skip to content


  • Research article
  • Open Access

Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana

  • 2,
  • 1,
  • 1,
  • 1,
  • 1 and
  • 1Email author
BMC Plant Biology201010:43

  • Received: 20 October 2009
  • Accepted: 7 March 2010
  • Published:



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.


  • High Light
  • Methyl Viologen
  • High Light Condition
  • High Light Treatment
  • Growth Light


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 [3] and have been identified in a variety of cellular compartments including cytosol [4], mitochondria [5], endoplastic reticulum [6], and chloroplasts [7]. Some of the DnaJ proteins also bind to the plasma membrane [8].

DnaJ proteins belong to a large family with several members: 22 in yeast [1], 41 in humans [9] and at least 89 in Arabidopsis [10]. 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 [11]. 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 [12]. It has been found that ATJ11, a chloroplast stroma localized DnaJ protein, is ubiquitously expressed in all plant organs examined so far [7]. DnaJ proteins found in the Arabidopsis chloroplast thylakoid proteome are likely to be important in thylakoid biogenesis [13]. Indeed, in Chlamydomonas, one chloroplast-targeted DnaJ protein was demonstrated to function in biogenesis of the thylakoid membrane [14].

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 [1]. According to public microarray databases their gene expression patterns resemble each other [15]. We previously found that AtJ8 gene is upregulated in darkness [16] similar to that of AtJ20 gene (Supplementary material in [16]). 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

Arabidopsis plants lacking a DnaJ protein AtJ8 (At1 g80920), AtJ11 (At4 g36040) or AtJ20 (At4 g13830) did not exhibit significantly different phenotypes compared to wild-type (WT) except for slightly stunted growth of the j11 and j20 mutants (Figure 1A and 1B). Photochemical efficiency of photosystem II (PSII) (Fv/Fm ratio) was not different between the WT and the DnaJ mutants under growth light (GL) conditions, whereas, it decreased somewhat more drastically in the mutants after exposure of 6 h to high light (HL) (1000 μmol photons m-2 s-1), especially in j11 and j20 as compared to that in WT (Figure 1C). When plants were returned to GL conditions, the PSII photochemical efficiency recovered quickly and no differences were found between the WT and mutants (Figure 1C). The other mutant lines for the AtJ11 and AtJ20 proteins exhibited similar phenotypes as described above (Additional file 1).
Figure 1
Figure 1

Phenotypes of DnaJ protein knockout mutants. A, Images of 4-week old wild-type (WT) and j8, j11 and j20 mutants; B, Contents of leaf chlorophyll in WT and the DnaJ mutants under growth light condition (120 μmol photons m-2 s-1), the values are means ± SD (n = 10) of ten independent experiments; C, PSII photochemical efficiency of DnaJ mutants, the values are means ± SD (n = 10) of ten independent experiments. WT, wild-type; GL, growth light (120 μmol photons m-2 s-1); HL, high light (1000 μmol photons m-2 s-1).

Localization of the three DnaJ proteins

In order to examine the localization of the three small DnaJ proteins, an antiserum for each protein was raised in rabbits using specific synthetic peptides. Despite purification of the antisera, we did not get good reactions using leaf total protein extracts (data not shown). However, as shown in Figure 2, the protein extracts from intact chloroplasts gave a specific band in WT around 17 kD, 15 kD, and 20 kD when the AtJ8, AtJ11 and AtJ20 antisera, respectively, were used, and importantly, the specific band was missing from the respective DnaJ mutant. This indicates that chloroplasts are at least one of the compartments containing these small DnaJ proteins in Arabidopsis. It should be noted that the size of each DnaJ protein in chloroplasts is somewhat lower than the predicted molecular mass (18.3-, 17.8- and 23.4-kD for AtJ8, AtJ11 and AtJ20, respectively). This is apparently due to the processing of the preprotein after import to chloroplast. In fact, Orme et al. reported that AtJ11 is located in chloroplast stroma and the mature protein has a molecular mass of 14.3 kD [7].
Figure 2
Figure 2

Immunodetection of the three DnaJ proteins AtJ8, AtJ11 and AtJ20 in chloroplasts. Chloroplasts were isolated from the leaves of WT and respective mutants after 3 h treatment in darkness. Total chloroplast proteins were used for immunoblotting, and for immunodetection of the AtJ8 protein, 30 μg protein was loaded whereas for immunodetection of AtJ11 and AtJ20 proteins, 100 μg protein was loaded. WT, wild-type.

Capacity of CO2assimilation

To analyse whether the DnaJ proteins are involved in acquiring the maximal CO2 fixation capacity, we measured both the light response and CO2 response curves of the DnaJ mutants and WT. The light response curves showed the maximum CO2 assimilation rate at 500 μmol photons m-2 s-1 which then decreased with increasing photosynthetic photon flux density (PPFD) in both WT and the DnaJ mutants (Figure 3A). Compared to WT, the DnaJ mutants possessed lower CO2 assimilation, especially the j20 mutant. Relatively, the assimilation of j8 was only slightly lower as compared to WT, showing that the AtJ8 protein is less related to the light-dependent regulation of CO2 fixation. Nonetheless, the CO2 response curves revealed lower CO2 assimilation in j8 as compared to that in WT (Figure 3B). The A-Ci curves based on intracellular CO2 concentration less than 300 μmol mol-1 demonstrated a lower Rubisco activity in all three DnaJ mutants as deduced from lower slope values of the curves as compared to WT, especially for j8 (Figure 3C). Although the amount of the Rubisco protein (large subunit and small subunit) did not obviously differ between WT and the DnaJ mutants, an immunoblot analysis of Rubisco Activase showed reduced amounts of this enzyme under light conditions in the DnaJ mutants as compared to WT (Figure 3D).
Figure 3
Figure 3

Capacity of CO 2 assimilation in DnaJ mutants and WT. A, Light response curves; B, CO2 response curves; C, A-Ci curves which based on intracellular CO2 concentration less than 300 μmol mol-1; D, Immunoblot analysis of Rubisco Activase, Rubisco large subunit (Rubisco LU) and small subunit (Rubisco SU) in leaves collected from growth light conditions and from darkness. Total proteins were isolated from leaves after 6 h illumination under growth light and in the end of the diurnal dark period. 10 μg of leaf total proteins was loaded. Protein quantification (indicated below the blots as a percentage of protein from that present in WT in the light) is based on three independent immunoblot experiments (mean ± SD). A, CO2 assimilation; Ci, intracellular CO2 consentration; PPFD, photosynthetic photon flux density. WT, wild-type; GL, growth light (120 μmol photons m-2 s-1).

Stabilization of PSII dimers and supercomplexes under high light illumination

Since the absence of one of the DnaJ proteins, AtJ8, AtJ11 or AtJ20, pronouncedly affected the photosynthetic capacity of respective mutants, we next investigated whether the DnaJ proteins are involved in regulation of the stability of the photosynthetic pigment protein complexes in the thylakoid membrane. Based on Blue-native gel electrophoretic (BN-PAGE) separation of thylakoid protein complexes (Figure 4A), the amount of PSII-LHCII supercomplexes was less in the DnaJ mutants than in WT after 6 h HL illumination (1000 μmol photons m-2 s-1). Immunoblotting of the BN-gels with D1 antibody more clearly showed the decrease of PSII supercomplexes in the mutants after the HL treatment. Moreover, the amount of PSII dimers also significantly decreased in the DnaJ mutants upon the HL treatment, especially in j11 and j20 (Figure 4A). To get more insights into the function of the three DnaJ proteins in the maintenance of the PSII oligomers, a long-term treatment under HL was employed. As shown in Figure 4B, the PSII supercomplexes completely disappeared both from WT and the DnaJ mutants whereas the PSII dimers were much more stable in WT than in the DnaJ mutants in the course of the long-term HL treatment. As compared to WT, the DnaJ mutants j11 and j20 showed a total disappearance of PSII dimers already during 24 h of HL treatment (Figure 4B), and clearly more of CP43 proteins had released from PSII complexes at this time point as compared to WT or the j8 mutant. As the total amounts of the D1, D2, CP43, CF1 and NDH-H proteins were similar in WT and the three mutants even after the HL treatment (deduced from PAGE and immunoblotting - see Additional file 2), it can be concluded that the three DnaJ proteins do not participate in the biosynthesis of individual PSII core proteins, but only provide stability for the PSII protein complexes.
Figure 4
Figure 4

BN-PAGE analysis of thylakoid protein complexes from WT and the DnaJ mutants. Thylakoids corresponding 4 μg Chl were loaded in each lane. A, A BN gel of thylakoid protein complexes from plants exposed to growth light conditions for 6 h and from plants exposed to high light for 6 h. Top panel, BN gel directly after electrophoresis; lower panel, BN gel immunoblotted with D1 antibody. B, Immunoblots of the BN gels prepared from plants after a long-term high light (1000 μmol photons m-2 s-1) exposure. Thylakoid membrane protein complexes of WT and the DnaJ mutants were subjected to Blue-native gel electrophoresis following immunoblotting with D1 (top panel) and CP43 (lower panel) antibodies. GL, 120 μmol photons m-2 s-1 growth light; HL, 1000 μmol photons m-2 s-1 high light.

Energy distribution between PSI and PSII and phosphorylation of the PSII-LHCII proteins

The 77 K chlorophyll fluorescence emission ratio F733/F685 was recorded as an indication of energy distribution between the PSI and PSII complexes (Figure 5A). The ratio of F733/F685 was slightly lower in the DnaJ mutants than in WT both when measured from dark acclimated and from GL acclimated plants. After HL illumination no clear differences in F733/F685 ratio were found between the WT and mutants with one exception, the ratio was higher in j11 as compared to that in WT after 500 μmol photons m-2 s-1 HL illumination (Figure 5A). To evaluate whether the phosphorylation of PSII proteins is related to redistribution of energy in plants lacking the DnaJ proteins, the phosphorylation levels of the major PSII phosphoproteins D1, D2, CP43 and LHCII were determined by immunoblotting with the P-Thr antibody. As can be seen in Figure 5B, only extremely weak phosphorylation of LHCII (P-LHCII) was detected in darkness and P-LHCII strongly accumulated in light conditions. Higher intensity light (1000 μmol photons m-2 s-1) decreased the level of P-LHCII but did this less efficiently in the DnaJ mutants than in WT (Figure 5B). Interestingly, LHCII was phosphorylated to the same level in all strains under GL and moderate HL (500 μmol photons m-2 s-1), despite clear differences in the 77 K fluorescence ratio under these two light conditions.
Figure 5
Figure 5

The 77 K fluorescence emission ratio F733/F685 and the thylakoid protein phosphorylation in WT and the DnaJ mutants. A, F733/F685 ratio in WT and the DnaJ mutants after 6 h treatment of plants under different light conditions. The values are means ± SD (n = 9~12) of three independent experiments with 3 to 4 replicates. B, Phosphorylation levels of thylakoid proteins after similar light treatments of plants as in A. C, Changes in thylakoid protein phosphorylation during a long-term high light (1000 μmol photons m-2 s-1) treatment. Thylakoid membranes were isolated from leaves after treatment of plants in darkness and after illumination at growth light and high light conditions for time periods indicated. 1.0 μg of chlorophyll was loaded to the wells for immunoblotting with p-thr antibody. WT, wild-type; D, darkness; GL, 120 μmol photons m-2 s-1 growth light; HL-500, 500 μmol photons m-2 s-1high light; HL-1000, 1000 μmol photons m-2 s-1 high light.

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 [17].

Gene expression profiles

Based on somewhat similar effects on photosynthetic parameters of the knockout of any of the three small chloroplast targeted DnaJ proteins, it was of interest to analyse the gene expression profiles of these mutants. The expression of about 1,200 genes showed more than two-fold changes in WT by HL treatment, and among those genes one third were upregulated (Figure 6, Additional file 3). It was interesting to note that the gene expression profiles of the mutants showed similarities under both GL and HL conditions to the HL-treated WT, although the expression levels somewhat varied in each mutant (Figure 6). More than half of genes changing expression were found to be coregulated between the DnaJ mutants, and all three mutants shared 556 and 687 coregulated genes under GL and HL, respectively, indicating their very similar response between the DnaJ mutants (Figure 7A). In each mutant, the expression of roughly 700 genes had changed independently of the growth light condition (Figure 7B). It is also worth noting that the j11 and j20 mutants showed more divergent gene expression (920 and 1047 genes, respectively) at growth light from that in WT as compared to j8 (560 genes) whereas after HL treatment the reverse situation was recorded (Figure 7B). However, although the three DnaJ proteins are localized in the chloroplasts, most of the genes related to thylakoid membranes were not affected by lacking of one of the small DnaJ proteins (Additional file 4).
Figure 6
Figure 6

Gene expression-profilings of the DnaJ mutants with comparison to WT. Genes whose expression showed more than a two-fold change (up- or down-regulated) with the p-value less than 0.05 and the B-value more than 2.0 were selected for making the heatmaps using the R program and Bioconductor packages. The values are averages from three independent biological replicates starting from the growth of a new set of plants. The heatmap marked by WT shows the changes of gene expression in WT after 6 h illumination at 1000 μmol photons m-2 s-1 against 6 h illumination at 120 μmol photons m-2 s-1. The heatmaps marked by the names of the DnaJ mutant show the changes of gene expression in each mutant against WT under both GL and HL conditions after 6 h illumination. WT, wild-type; GL, 120 μmol photons m-2 s-1 growth light; HL, 1000 μmol photons m-2 s-1 high light. (red, upregulated; green, downregulated; black, missing value).

Figure 7
Figure 7

Venn diagrams of genes impacted by a HL treatment and by a DnaJ protein knockout. A, More than half of the genes changing expression are coregulated in the three DnaJ mutants and the mutants share 556 and 687 coregulated genes under GL and HL conditions, respectively. B, Coregulation analysis of gene expression between GL and HL conditions for each DnaJ mutant. WT, wild-type; GL, 120 μmol photons m-2 s-1 growth light; HL, 1000 μmol photons m-2 s-1 high light.

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

Based on the cues from microarray results, we next tested some oxidative stress responses of the DnaJ mutants. At first, the H2O2 levels in the leaves of the DnaJ mutants and WT were detected using DAB (diaminobenzidine) as a substrate. Notably, the staining intensity and accordingly the level of H2O2 in the DnaJ mutants was lower as compared to WT, especially in plants illuminated under HL for 6 h (Figure 8A). Since ascorbate peroxidases (APXs) and chloroplast peroxiredoxins (PRXs) associated with the water-water cycle, are generally known protectants of chloroplasts against oxidative damage, the contents of these H2O2-detoxifying enzymes were evaluated by immunoblotting. As shown in Figure 8B, the amounts of all these enzymes, including tAPX (thylakoid APX), sAPX (stroma APX), cAPX (cytoplasmic APX), and two PRXs, PrxE (peroxiredoxin E) and 2-Cys Prx (2-cysteine peroxiredoxin), were pronouncedly higher in the three DnaJ mutants as compared to WT no matter whether the plants were subjected to darkness, GL or HL conditions before measurements. Nevertheless, higher amounts of these enzymes were present in the light conditions, especially in HL. These results suggest that the higher amounts of H2O2-detoxifying enzymes contributed to the lower H2O2 levels in the mutants.
Figure 8
Figure 8

Production of ROS and the stress tolerance of WT and the DnaJ mutant j8 , j11 and j20. A, Histochemical detection of H2O2 in the leaves with DAB staining after 6 h incubation of leaves under GL (120 μmol photons m-2 s-1) and HL (1000 μmol photons m-2 s-1). B, Immunoblots depicting the levels of H2O2-detoxifying enzymes in WT and the DnaJ mutant leaves after 6 h incubation of plants under different light conditions. 10 μg of the leaf total proteins loaded. C, Ion leakage induced by 6 h HL (1000 μmol photons m-2 s-1) illumination of leaves in the presence and absence of Methyl viologen (MV), the values are means ± SD (n = 8) of two independent experiments with 4 replicates. D, OxyBlot of leaf total proteins (10 μg proteins loaded) after treatment of plants at different light intensities. GL, 120 μmol photons m-2 s-1 growth light; HL-1, 500 μmol photons m-2 s-1 high light; HL-2, 1000 μmol photons m-2 s-1 high light. WT, wild-type.

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 [1], 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 [20]. 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 [21].

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 [22], 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 [23]. 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 [23]. 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 [17]. 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 [17].

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 [24]. 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 [25] 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 [26], 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 [25] whereas over-tAPX is a transgenic line which overexpresses the thylakoid-bound ascorbate peroxidase [27]. 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 [28], and by the CSN mutants [29]. The most studied CSN function is the regulation of protein degradation and beyond this, the CSN also acts as a transcriptional regulator [30].


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 [32]. 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 [33] and Porra et al. [34] 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. [26]. 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 [17] and the thylakoid membranes as described by Suorsa et al. [35]. 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 [36] (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 [36]. 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 [37]. APXs and PRXs antibodies were obtained as described previously [32]. 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. [38]. 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. [32]. 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. [32].

Microarray analysis

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 [16] and subsequently followed as described by Kangasjärvi et al. [32]. 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 [39]. 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.

Authors’ Affiliations

Department of Biochemistry and Food Chemistry, Plant Physiology and Molecular Biology, University of Turku, FI-20014 Turku, Finland
Institute of Crop Sciences, College of Agriculture and Biotechnology, Zhejiang University, 310029 Hangzhou, China


  1. Walsh P, Bursac D, Law YC, Cyr D, Lithgow T: The J-protein family: modulating protein assembly, disassembly and translocation. EMBO Rep. 2004, 5: 567-571. 10.1038/sj.embor.7400172.PubMedPubMed CentralView ArticleGoogle Scholar
  2. Liberek K, Lewandowska A, Zietkiewicz S: Chaperones in control of protein disaggregation. EMBO J. 2008, 27: 328-335. 10.1038/sj.emboj.7601970.PubMedPubMed CentralView ArticleGoogle Scholar
  3. Cheetham ME, Caplan AJ: Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function. Cell Stress Chaperon. 1998, 3: 28-36. 10.1379/1466-1268(1998)003<0028:SFAEOD>2.3.CO;2.View ArticleGoogle Scholar
  4. Thomas JG, Baneyx F: Protein folding in the cytoplasm of Escherichia coli: requirements for the DnaK-DnaJ-GrpE and GroEL-GroES molecular chaperone machines. Mol Microbiol. 1996, 21: 1185-1196. 10.1046/j.1365-2958.1996.651436.x.PubMedView ArticleGoogle Scholar
  5. Voos W, Rottgers K: Molecular chaperones as essential mediators of mitochondria biogenesis. Biochim Biophys Acta. 2002, 1592: 52-62.View ArticleGoogle Scholar
  6. Nicoll WS, Boshoff A, Ludewig MH, Hennessy F, Jung M, Blatck GL: Approaches to the isolation and characterization of molecular chaperones. Protein Expres Purif. 2006, 46: 1-15. 10.1016/j.pep.2005.08.005.View ArticleGoogle Scholar
  7. Orme W, Walker AR, Gupta R, Gray JC: A novel plastid-targeted J-domain protein in Arabidopsis thaliana. Plant Mol Biol. 2001, 46: 615-626. 10.1023/A:1010665702621.PubMedView ArticleGoogle Scholar
  8. Porschewski P, Specht V, Stubner S, Kindl H: A novel tetratricopeptide repeat-containing J-protein localized in a plasma membrane-bound protein complex of the phytopathogenic oomycete Phytophthora megasperma. Euro J Cell Biol. 2001, 80: 527-538. 10.1078/0171-9335-00188.View ArticleGoogle Scholar
  9. Qiu XB, Shao YM, Miao S, Wang L: The diversity of the DnaJ/Hsp40 family, the crucial partners for Hsp70 chaperones. Cell Mol Life Sci. 2006, 63: 2560-2570. 10.1007/s00018-006-6192-6.PubMedView ArticleGoogle Scholar
  10. Miernyk JA: The J-domian proteins of Arabidopsis thaliana: an unexpectedly large and diverse family of chaperones. Cell Stress Chaperon. 2001, 6: 209-218. 10.1379/1466-1268(2001)006<0209:TJDPOA>2.0.CO;2.View ArticleGoogle Scholar
  11. Liu C, Willmund F, Golecki JR, Cacae S, Heâ B, Markert C, Schroda M: The chloroplast HSP70B-CDJ2-CGE1 chaperones catalyse assembly and disassembly of VIPP1 oligomers in Chlamydomonas. Plant J. 2007, 50: 265-277. 10.1111/j.1365-313X.2007.03047.x.PubMedView ArticleGoogle Scholar
  12. Vitha S, Froehlich JE, Koksharova O, Pyke KA, van Erp H, Osteryoung KW: ARC6 is a J-domain plastid division protein and an evolutionary descendant of the cyanobacterial cell division protein Ftn2. Plant Cell. 2003, 15: 1918-1933. 10.1105/tpc.013292.PubMedPubMed CentralView ArticleGoogle Scholar
  13. Friso G, Giacomelli L, Ytterberg AJ, Peltier JB, Rudella A, Sun Q, van Wijk KJ: In-depth analysis of the thylakoid membrane proteome of Arabidopsis thaliana chloroplasts: New proteins, new functions, and a plastid proteome database. Plant Cell. 2004, 16: 478-499. 10.1105/tpc.017814.PubMedPubMed CentralView ArticleGoogle Scholar
  14. Liu C, Willmund F, Whitelegge JP, Hawat S, Knapp B, Lodha M, Schroda M: J-Domain protein CDJ2 and HSP70B are a plastidic chaperone pair that interacts with vesicle-inducing protein in plastids. Mol Biol Cell. 2005, 16: 1165-1177. 10.1091/mbc.E04-08-0736.PubMedPubMed CentralView ArticleGoogle Scholar
  15. Obayashi T, Kinoshita K, Nakai K, Shibaoka M, Hayashi S, Saeki M, Shibata D, Saito K, Ohta H: ATTED-II: a database of co-expressed genes and cis elements for identifying co-regulated gene groups in Arabidopsis. Nucleic Acids Res. 2007, 35: D863-D869. 10.1093/nar/gkl783.PubMedPubMed CentralView ArticleGoogle Scholar
  16. Piippo M, Allahverdiyeva Y, Paakkarinen V, Suoranta U-M, Battchikova N, Aro E-M: Chloroplast-mediated regulation of nuclear genes in Arabidopsis thaliana in the absence of light stress. Physiol Genomics. 2006, 25: 142-152. 10.1152/physiolgenomics.00256.2005.PubMedView ArticleGoogle Scholar
  17. Vainonen JP, Sakuragi Y, Stael S, Tikkanen M, Allahverdiyeva Y, Paakkarinen V, Aro E, Suorsa M, Scheller HV, Vener A, Aro E-M: Light regulation of Cas, a novel phosphoprotein in the thylakoid membrane of Arabidopsis thaliana. FEBS J. 2008, 275: 1767-1777. 10.1111/j.1742-4658.2008.06335.x.PubMedView ArticleGoogle Scholar
  18. Long SP, Bernacchi CJ: Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error. J Exp Bot. 2003, 54: 2393-2401. 10.1093/jxb/erg262.PubMedView ArticleGoogle Scholar
  19. Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL: Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant Cell Environ. 2007, 30: 1035-1040. 10.1111/j.1365-3040.2007.01710.x.PubMedView ArticleGoogle Scholar
  20. Portis AR, Li C, Wang D, Salvucci ME: Regulation of Rubisco activase and its interaction with Rubisco. J Exp Bot. 2008, 59: 1597-1604. 10.1093/jxb/erm240.PubMedView ArticleGoogle Scholar
  21. Gao H, Sage TL, Osteryoung KW: FZL, an FZO-like protein in plants, is a determinant of thylakoid and chloroplast morphology. Proc Natl Acad Sci USA. 2006, 103: 6759-6764. 10.1073/pnas.0507287103.PubMedPubMed CentralView ArticleGoogle Scholar
  22. Tikkanen M, Nurmi M, Suorsa M, Danielsson R, Mamedov F, Styring S, Aro E-M: Phosphorylation-dependent regulation energy distribution between the two photosystems in higher plants. Biochim Biophys Acta. 2008, 1777: 425-432. 10.1016/j.bbabio.2008.02.001.PubMedView ArticleGoogle Scholar
  23. Aro E-M, Ohad I: Redox regulation of thylakoid protein phosphorylation. Antioxid Redox Signal. 2003, 1: 55-67. 10.1089/152308603321223540.View ArticleGoogle Scholar
  24. Vandenbroucke K, Robbens S, Vandepoele K, Inzé D, Peer Van de Y, Van Breusegem F: Hydrogen peroxide-induced gene expression across kingdoms: A comparative analysis. Mol Biol Evol. 2008, 25: 507-516. 10.1093/molbev/msm276.PubMedView ArticleGoogle Scholar
  25. Zhang J, Addepalli B, Yun K-Y, Hunt AG, Xu R, Rao S, Li QQ, Falcone DL: A polyadenylation factor subunit implicated in regulating oxidative signaling in Arabidopsis thaliana. PloS ONE. 2008, 3 (6): e2410-10.1371/journal.pone.0002410.PubMedPubMed CentralView ArticleGoogle Scholar
  26. Soitamo AJ, Piippo M, Allahverdiyeva Y, Battchikova N, Aro E-M: Light has a specific role in modulating Arabidopsis gene expression at low temperature. BMC Plant Biol. 2008, 8: 13-10.1186/1471-2229-8-13. doi:10.1186/1471-2229-8-13PubMedPubMed CentralView ArticleGoogle Scholar
  27. Laloi C, Stachowiak M, Pers-Kamczyc E, Warzych E, Murgia I, Apel K: Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana. Proc Natl Acad Sci USA. 2007, 104: 672-677. 10.1073/pnas.0609063103.PubMedPubMed CentralView ArticleGoogle Scholar
  28. Sangster TA, Bahrami A, Wilczek A, Watanabe E, Schellenberg K, McLellan C, Kelley A, Kong SW, Queitsch C, Lindquist S: Phenotypic diversity and altered environmental plasticity in Arabidopsis thaliana with reduced Hsp90 levels. PloS ONE. 2007, 2 (7): e648-10.1371/journal.pone.0000648.PubMedPubMed CentralView ArticleGoogle Scholar
  29. Dohmann EMN, Levesque MP, Isono E, Schmid M, Schwechheimer C: Auxin responses in mutants of the Arabidopsis CONSTITUTIVE PHOTOMORPHOGENIC9 signalosome. Plant Physiol. 2008, 147: 1369-1379. 10.1104/pp.108.121061.PubMedPubMed CentralView ArticleGoogle Scholar
  30. Chamovitz DA: Revisiting the COP9 signalosome as a transcriptional regulator. EMBO Rep. 2009, 10: 352-358. 10.1038/embor.2009.33.PubMedPubMed CentralView ArticleGoogle Scholar
  31. Koussevitzky S, Nott A, Mockler TC, Hong F, Sachetto-Martins G, Surpin M, Lim J, Mittler R, Chory J: Signals from chloroplasts converge to regulate nuclear gene expression. Science. 2007, 316: 715-719. 10.1126/science. 1140516.PubMedView ArticleGoogle Scholar
  32. Kangasjärvi S, Lepistö A, Hännikäinen K, Piippo M, Luomala EM, Aro EM, Rintamäki E: Diverse roles for chloroplast stromal and thylakoid-bound ascorbate peroxidases in plant stress responses. Biochem J. 2008, 412: 275-285. 10.1042/BJ20080030.PubMedView ArticleGoogle Scholar
  33. Inskeep WP, Bloom PR: Extinction coefficients of chlorophyll a and b in N, N-dimethylformamide and 80% acetone. Plant Physiol. 1985, 77: 483-485. 10.1104/pp.77.2.483.PubMedPubMed CentralView ArticleGoogle Scholar
  34. Porra RJ, Thompson WA, Kriedemann PE: Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophyll a and b with four different solvents: verification of the concentration of chlorophyll by atomic absorption spectroscopy. Biochim Biophys Acta. 1989, 975: 384-394. 10.1016/S0005-2728(89)80347-0.View ArticleGoogle Scholar
  35. Suorsa M, Regel RE, Paakkarinen V, Battchikova N, Herrmann RG, Aro E-M: Protein assembly of photosystem II and accumulation of subcomplexes in the absence of low molecular weight subunits PsbL and PsbJ. Euro J Biochem. 2004, 271: 96-107. 10.1046/j.1432-1033.2003.03906.x.View ArticleGoogle Scholar
  36. Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970, 227: 680-685. 10.1038/227680a0.PubMedView ArticleGoogle Scholar
  37. Rintamäki E, Martinsuo P, Pursiheimo S, Aro EM: Cooperative regulation of light-harvesting complex II phosphorylation via the plastoquinol and ferredoxin-thioredoxin system in chloroplasts. Proc Natl Acad Sci USA. 2000, 97: 11644-11649. 10.1073/pnas.180054297.PubMedPubMed CentralView ArticleGoogle Scholar
  38. Rokka A, Suorsa M, Saleem A, Battchikova N, Aro EM: Synthesis and assembly of thylakoid protein complexes: multiple assembly steps of photosystem II. Biochem J. 2005, 388: 159-168. 10.1042/BJ20042098.PubMedPubMed CentralView ArticleGoogle Scholar
  39. Smyth GK: Limma: linear models for microarray data. Bioinformatics and Computational Biology Solutions using R and Bioconductor. Edited by: Gentleman R, Carey V, Dudoit S, Irizarry R, Huber W. 2005, New York: Springer, 397-420. full_text.View ArticleGoogle Scholar


© Chen et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.