Original Research ARTICLE
Impaired Function of the Calcium-Dependent Protein Kinase, OsCPK12, Leads to Early Senescence in Rice (Oryza sativa L.)
- 1Key Laboratory for Zhejiang Super Rice Research and State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China
- 2College of Agronomy, Gansu Agricultural University, Lanzhou, China
- 3Nanchong Academy of Agricultural Sciences, Nanchong, China
- 4Rice Research and Training Center, Field Crops Research Institute, Agriculture Research Center, Kafr El Sheikh, Egypt
Premature leaf senescence affects plant yield and quality, and numerous researches about it have been conducted until now. In this study, we identified an early senescent mutant es4 in rice (Oryza sativa L.); early senescence appeared approximately at 60 dps and became increasingly senescent with the growth of es4 mutant. We detected that content of reactive oxygen species (ROS) and malondialdehyde (MDA), as well as activity of superoxide dismutase (SOD) were elevated, while chlorophyll content, soluble protein content, activity of catalase (CAT), activity of peroxidase (POD) and photosynthetic rate were reduced in the es4 mutant leaves. We mapped es4 in a 33.5 Kb physical distance on chromosome 4 by map-based cloning. Sequencing analysis in target interval indicated there was an eight bases deletion mutation in OsCPK12 which encoded a calcium-dependent protein kinase. Functional complementation of OsCPK12 in es4 completely restored the normal phenotype. We used CRISPR/Cas9 for targeted disruption of OsCPK12 in ZH8015 and all the mutants exhibited the premature senescence. All the results indicated that the phenotype of es4 was caused by the mutation of OsCPK12. Overexpression of OsCPK12 in ZH8015 enhanced the net photosynthetic rate (Pn) and chlorophyll content. OsCPK12 was mainly expressed in green organs. The results of qRT-PCR analysis showed that the expression levels of some key genes involved in senescence, chlorophyll biosynthesis, and photosynthesis were significantly altered in the es4 mutant. Our results demonstrate that the mutant of OsCPK12 triggers the premature leaf senescence; however, the overexpression of OsCPK12 may delay its growth period and provide the potentially positive effect on productivity in rice.
Senescence is a series of deteriorative processes including death and decomposition of cell, degradation of organization and organ, and the aging of the life function. Leaf senescence as a type of programmed cell death (PCD) is a critical process for the adaptability of plants (Himelblau, 2000). As a complex physiological process, leaf senescence is not only influenced by external environment such as temperature, light, drought, nutrient deficiency, wounding, pathogen infection, etc. (Yang et al., 2011), but also affected by internal genetic factors such as developmental stage and phytohormone levels (Yang et al., 2016). Premature leaf senescence has a direct impact on crop yields by changing the duration of photosynthesis, and modifying the nutrient remobilization efficiency and harvest index (Wu et al., 2012). As one of the major food crops, rice feeds nearly half of the world’s population, but rice leaf premature senescence often results in the reduction in yield and quality. On the contrary, delayed leaf senescence shows potentially positive effects on rice productivity. Therefore, understanding the molecular mechanism of leaf senescence is important for breeders in raising rice production and quality.
Many rice leaf senescence-associated genes have been identified from different plant species. These genes can be divided into different categories according to the metabolic pathways. One type of genes synthesize chloroplast and degrade chlorophyll including NYC1, NOL, OsPAO, OsRCCR1, OsSGR, V1, V2 and so on (Jiang et al., 2007; Kusaba et al., 2007; Kusumi et al., 2011; Tang et al., 2011). The second type involved in synthesizing, degrading and transporting proteins including GnT1, OsSAG12, Osh69, TDC1, TDC2, etc. (RH et al., 2004; Kang et al., 2009; Fanata et al., 2013; Singh et al., 2013). The third type of genes involve in the hormone signaling pathway. For example, OsFBK12, OsSAMS1, ein2, and EIN3 involved in ethylene signaling pathways (Alonso et al., 1999; Chen et al., 2013; Li et al., 2013). PCD-related genes belong to the fourth type of genes, which play an important role in the process of aging. RLS1 encodes a previously uncharacterized NB-ARM protein regulating PCD during leaf senescence (Jiao et al., 2012). In addition, three transcription factor families including NAC, WRKY, and TCP involved in leaf senescence. OsY37, an NAC transcription factor gene positively regulates the heading date and senescence during the reproductive phase in rice (El Mannai et al., 2017). Although great progress has been made on rice leaf senescence research, rice leaf senescence is a complex process which involves many genes and metabolic pathways. The molecular mechanisms of leaf senescence are still remain unclear and further work about it should be done.
Calcium-dependent protein kinases (CPKs) as a type of calcium sensor, which contain a kinase catalytic domain and an autoinhibitory “junction” domain, followed by a calmodulin-like, a regulatory domain (Hrabak et al., 2003). CPKs perform multiple biological function in plants such as senescence and cell death, hormones signal transduction, stress and defense responses, growth and development, carbon and nitrogen metabolism, formation of cytoskeleton, regulation of ion channels, etc. (Lei et al., 2007). For example, NtCDPK1 and NtRpn3 are expressed in rapidly growing tissues, and knocking down protein expression led to severe growth defects with abnormal cell morphology and premature cell death of newly developing leaves (Simeunovic et al., 2016). A 57 kD calcium-dependent protein kinase (CDPK) molecule has multiple sites for autophosphorylation, and the changes in in vivo autophosphorylation status of the 57 kD CDPK induced by ST (Senescence-inducing treatment) may play an important role in regulating the catalytic activity of leaf senescence in Soybean Primary Leaves (Wang et al., 2001). CPK10 plays important roles in ABA and Ca2+-mediated regulation of stomatal movements possibly by interacting with HSP1 (Zou et al., 2010). OsCPK21 is involved in the positive regulation of the signaling pathways that are involved in the response to ABA and salt stress (Asano et al., 2011). OsCPK4 is a positive regulator of the salt and drought stress responses in rice via the protection of cellular membranes from stress-induced oxidative damage (Campo et al., 2014). AtCPK6 is functionally redundant and a positive regulator involved in the tolerance to salt/drought stress in Arabidopsis (Xu et al., 2010). Rice SPK, a calcium-dependent protein kinase, is expressed uniquely in the endosperm of immature seed, and SPK is involved in the activation of Suc synthase that may be important for supplying substrates for the biosynthesis of storage products (Asano et al., 2002). CPK11 and CPK24 together mediate the Ca2+-dependent inhibition of K+ channels and participate in the regulation of pollen tube growth in Arabidopsis (Zhao et al., 2013). The phosphorylation of Sucrose phosphate synthetase (SPS) and nitrate reductase (NR) might be conducted by one CPK (Chung et al., 1999). Putnam’s study indicated that CPK was bound with actin filament in pollen tube and internodal cell (Putnam et al., 1989). CPKs also regulated ion channels in guard cell vacuolar membrane (Pei et al., 1996) and inward K+ channel of plasmalemma (Li et al., 1998; Berkowitz et al., 2000). Besides CPKs are related with stomatal movement, metabolism of enzymes, membrane transport and many other biologic functions and more and more functions of CDPK family members will be identified. Multifunctional CPKs are found in both vascular and non-vascular plants (Harmon et al., 2001). There are 34 genes in Arabidopsis and 31 genes in rice encoding CPKs, respectively (Cheng et al., 2002; Ray et al., 2007).
In this study, we isolated and characterized an early senescent (es4) mutant in rice which displayed early leaf senescence phenotype along with lower seed setting rate and 1000-grain weight, less ROS, lower photosynthetic capacity and Chlorophyll content. Map-based cloning and sequencing analysis showed that the loss of eight bases led to a frame-shift mutation in OsCPK12 which encoded a calcium-dependent protein kinase. The following functional validation demonstrated that the mutation of OsCPK12 not only led to leaf senescence but also influenced the yield-related traits in rice.
Materials and Methods
The early senescence 4 (es4) mutant was isolated from a Co60 γ-ray treatment rice mutant library of the indica rice cultivar, ZH8015. The F2 population, derived from cross ZH8015 and 02428 (a japonica rice cultivar) was used for genetic analysis and mapping of es4. All the plants were grown in a paddy field under natural conditions in Hangzhou, Zhejiang province and in Lingshui, Hainan Province, China. The lower leaves of es4 firstly showed senescent phenotype at 60 days post-sowing (dps). In the F2 population, the plants with leaf senescence phenotype were used for fine genetic mapping.
Hydrogen Peroxide, Cell Death and Superoxide Anion Detection
Qualitative analysis of hydrogen peroxide (H2O2), cell death and superoxide anion was conducted by 3,3-diaminobenzidine (DAB), evans blue (EB) and nitroblue tetrazolium (NBT) staining as previously reported by Thordal-Christensen et al. (1997); Ramel et al. (2009) and Kong and Li (2011). The third leaves of ZH8015 and es4 mutant were taken from the plants grown in the paddy field at 70 dps.
The terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assays were performed using a Fluorescein In Situ Cell Death Detection Kit (Roche) following the manufacturer’s instructions. The methods were used for sectioning and fluorescence labeling as previously reported by He et al. (2018). The green fluorescence of fluorescein and blue fluorescence of DAPI were analyzed using a Carl Zeiss LSM 710 laser-scanning confocal microscope (Göttingen). The third leaves of ZH8015 and es4 mutant were taken from the plants grown in the paddy field at 70 dps.
Measurement of Chlorophyll Content and Photosynthetic Rates
The chlorophyll was extracted from the third upper leaves at 70 dps and determined according to Porra et al. (1994). The OD values under the wavelengths of 450, 663, and 646 nm were obtained with a DU800 visible spectrophotometer (BACKMAN COULTER DU800, United States). The content of Chlorophyll a and b were analyzed according to the method as described by Wellburn (1994).
At 9:00–11:00 on a sunny day, the net photosynthetic rate (Pn) of third upper leaves was determined by the portable photosynthesis measurement device LI-6400 (Li-COR, Lincoln, NB, United States) with 1200 μmol protons (m2.s) intensity and 500 μmol⋅s-1 airflow rate under field conditions at 70 dps. All experiments were repeated with three biological replicates. Student’s t-test was conducted by EXCEL2013 and multiple comparison was conducted by SAS 9.0.
Measurement of Enzymatic Activity and Senescence-Related Parameters
The activities of catalase (CAT), superoxide dismutase (SOD), peroxidase (POD), ascorbate peroxidase (APX) and the content of soluble protein (SP), H2O2 and malondialdehyde (MDA) were determined using commercial assay kits from Nanjing Jiancheng Bioengineering Research Institute (China). The third upper leaves of ZH8015 and es4 mutant were taken from the plants grown in the paddy field at 70 dps. Phenotypic values are the means of three biological replicates. Statistical analysis was conducted by EXCEL2013.
Observation of the Chloroplast Structure by Transmission Electron Microscopy
At 70 dps, the third leaves from ZH8015 and es4 were fixed using 2.5% glutaraldehyde in 0.2 M phosphate buffer (pH 7.0) for more than 16 h at 4°C. After three briefly rinsed in the phosphate buffer, the samples were treated with 1% (w/v) OsO4 in phosphate buffer (pH 7.0) at 4°C overnight and then dehydrated in a graded series of ethanol [30, 50, 70, 85, 95, and 100% (v/v)]. Ethanol was subsequently replaced by a series of Spurr’s resin dilutions [25, 50, 75, and 100% (v/v)] for approximately 15–20 min at each step. The samples were placed in a 1:1 mixture of alcohol and 90% acetone for 20 min at room temperature. Next, the samples were transferred into 90% acetone for 20 min and then into 100% acetone for dehydration treatment three times, 15 min every time. After dehydration treatment, the samples were transferred into a final Spurr resin mixture overnight. The specimens were then placed in capsules with embedding medium and heated at 70°C for 9 h. The specimen sections were stained using uranyl acetate and alkaline lead citrate for 15 min each and observed using a TEM (Model H-7650) at the institute of Agriculture and Biotechnology, Zhejiang University.
Map-Based Cloning of ES4
F1 plants derived from the cross between ZH8015 and 02428, were grown in the paddy field at Lingshui experimental Station of CNRRI in 2014 for determining dominance or recessiveness of ES4, and the F2 population was used for segregation analysis. 77 F2 individual plants with the mutant phenotype were used for preliminary mapping of the ES4. The initial mapping was conducted using 145 SSR and InDel markers scattered across 12 chromosomes in rice. To further narrow down the ES4 region, many new InDel markers were designed using Primer Premier 5.0 after comparing the sequences between Nipponbare and 93-11 in Gramene1. All the primers were synthesized by TsingKe technology company (Hangzhou, China). The marker information was presented in Supplementary Table S2. The DNA was extracted by cetyltriethyl ammonium bromide (CTAB) (Murry and Thompson, 1980). The PCR was performed using 2 × Taq PCR Mix from TsingKe technology company (Hangzhou, China). The reaction system and program of PCR referred specification. PCR products were visualized on 8.0% non-denaturing polyacrylamide gel using silver staining.
Plasmid Construction and Plant Transformation
For functional complementation of the es4 mutant, a 6745 bp genomic DNA that contains the ES4 coding region along with the upstream sequence and downstream sequences was amplified from wild-type ZH8015 by PCR using the ES4-COM primer (Supplementary Table S2), and then was introduced into the binary vector pCAMBIA1300 using the In-Fusion HD Cloning Kit (Clontech, Japan). We generated a 23 bp target sequence (5′-TCGACCGCATCACGGCCAAGGGG-3′) in CRISPR-P2. The target sequence was cloned into BGK03 vector which was digested by ECO31I and connected by T4-ligase. BGK03 vector (Biogle Company, China) contains a codon-optimized Cas9 driven by a maize strong promoter (UBI), the OsU6 promoter and gRNA scaffolds of Cas9 expression backbone vector (Li et al., 2016). To create the overexpression vector construct, a 1754-bp 5′ upstream region of the ES4 gene was amplified by PCR using ES4-OE primers (Supplementary Table S2), and the sequence was cloned into pCAMBIA2300 vector which was digested by SmaI and XbaI. All the constructs were checked by DNA sequencing. All vectors were transformed into ZH8015 or es4 mutant via the Agrobacterium tumefaciens-mediated transformation method. We used T3 transgenic plants for phenotypic investigation and physiological study.
RNA Extraction and qRT-PCR
Total RNA was isolated from rice organizations, including roots, stems, leaves, leaf sheaths, and panicles using the RNAprep Pure Plant Kit (TIANGEN, Beijing). The cDNA was converted from total RNA using ReverTra Ace qPCR-RT Master Mix (Toyobo, Japan). qRT-PCR was performed using SYBR premix Ex Taq II (Takala, Japan) in the LightCycler 480 II (Roche, Sweden) by the Methods and procedures of the manufacturer’s instructions. OsActin1 was used as control. The primers used for RT-PCR are listed in Supplementary Table S3. The 2-ΔCT and 2-ΔΔCT method was used to analyze the relative transcript levels in gene expression. Values are the means of three biological replicates. T-test and multiple comparison were conducted by EXCEL2013 and SAS 9.0, respectively.
Phenotype of the es4 Mutant
The es4 mutant exhibited a premature senescence leaf, dwarf and lower yield phenotype. There was no obvious phenotypic difference between es4 and ZH8015 at the early developmental stage. The tips and margins of the lower leaves of es4 became yellow approximately at 60 dps (Figures 1A,B); all leaves of the es4 became yellow and senescent at the grain-filling stage while most leaves of wild type were still green at the same time (Figure 1F). The plant height, spikelet number per panicle, seed setting rate and 1000-grain weight were remarkably decreased in the es4 mutant. Compared with ZH8015, spikelet number per panicle, seed setting rate and 1000-grain weight of es4 decreased by 16.14, 9.45, and 8.62%, respectively (Table 1). These results indicated that the early senescent leaves in es4 would negatively affect the grain yield.
Figure 1. Phenotypic characteristics of es4 and the wild-type ZH8015. (A) Phenotype of ZH8015 and es4 mutant at 70 dps. (B) A close up of the upper three leaves in ZH8015 and es4 mutant. (C) DAB staining. (D) Evans blue staining. (E) NBT staining. (F) Plant of ZH8015 and es4 at the mature stage. (G) The expression levels of senescence-related genes (mean ± S.D., n = 3). ∗ significance at P < 0.05, ∗∗ extremely significance at P < 0.01. Scale bar = 2 cm.
Table 1. Comparison of agronomic traits between wild type ZH8015 and mutant es4 (mean ± SD, n = 10).
Early senescence usually induces the accumulation of H2O2 in rice leaves. These toxic ROS can further result in lipid peroxidation, cellular damage and cell death. DAB staining showed that the color of es4 leaves is darker than those in ZH8015 as a result of more accumulation of H2O2 in early senescence leaves of es4 (Figure 1C). Evans blue staining is an indicator of irreversible membrane damage or cell death. After Evans blue staining, es4 exhibited a deep blue at the site of necrosis, however, leaves of ZH8015 exhibited slight blue (Figure 1D), indicating that there was more cell death in es4. Early senescence often leads more accumulation of Superoxide radicals concomitantly. As an indicator of Superoxide radicals’ accumulation, the results of NBT staining indicated that more blue formazan precipitates appeared in es4 leaves (Figure 1E). Therefore, there was more Superoxide radicals accumulation in es4. To confirm that there are more cell deaths in es4, the third leaves of es4 mutant and ZH8014 at 70 dps were subjected to a TUNEL assay. Few of the nuclei in leaf sections of ZH8015 were TUNEL positive, whereas numerous nuclei in leaf sections of es4 were TUNEL positive (Figure 2). The results of TUNEL assays indicated that there were more cell apoptosis in es4. We also analyzed the expression levels of some senescence-related genes, and the results indicated that the expression levels of senescence-related genes including OsI57, OsI85, and OsH36 were significantly upregulated in es4, but that OsAPX1 was significantly down regulated in es4 (Figure 1G). These results indicated that the mutation of ES4 generally induced accumulation of ROS, DNA damage and accelerated cell senescence in es4 leaves.
Figure 2. TUNEL assay the cell death. (A,B) ZH8015. (C,D) es4. Blue signal is DAPI staining, green color represents positive result. Scale bar = 75 μm.
Alteration of Photosynthetic Ability, Chlorophyll Content and Chloroplast Ultrastructure
Pn, content of Chlorophyll a and b were examined at 70 dps in ZH8015 and es4. Compared to the wild-type plants, the es4 mutant’s Pn, content of chlorophyll a and b was only 63.52, 22.45, and 16.54%, respectively (Figures 3E,F). These results indicated that es4 mutant exhibited reduction in net photosynthetic rate and content of chlorophyll a and b.
Figure 3. Ultrastructure of the chloroplast; senescence related-indices of ZH8015 and es4 at 70 dps. Photosynthetic ability analysis in flag leaves of ZH8015 and es4 at 70 dps. Senescence related-indices of ZH8015 and es4 at 70 dps. (A,C) Ultrastructure of the chloroplast in the flag leaf of ZH8015 at 70 dps. (B,D) Ultrastructure of the chloroplast in the flag leaf of es4 at 70 dps. CP, chloroplast; G, granum; M, mitochondrion; OG, osmiophilic granule; S, starch granule. Scale bar = 0.2 μm. (E) Content of chlorophyll a and b. (F) Net photosynthetic rate (Pn). (G) The enzymatic activities of catalase (CAT). (H) The content of H2O2. (I) The content of malondialdehyde (MDA). (J) The enzymatic activities of peroxidase (POD). (K) The enzymatic activities of superoxide dismutase (SOD). (L) The content of soluble proteins (SP) (mean ± SD, n = 3), ∗ significance at P < 0.05, ∗∗extremely significance at P < 0.01.
Transmission electron microscopy (TEM) analysis revealed that the number and size of chloroplasts were dramatically reduced in third leaves of es4 mutants compared to the leaves of wild-type plants. The cell of ZH8015 leaves exhibited integrated chloroplast membrane and orderly stroma lamellae structure (Figures 3A,B). Conversely, some chloroplasts membranes were dissolved and the thylakoids were disorderly arranged or degraded in es4 mutant leaves, and we also observed more osmiophilic granules and starch grains in es4 (Figures 3C,D). All the results indicated that the mutation of ES4 may lead to abnormal chloroplast development.
Determination of Physiological Parameters Related to Senescence
We measured the content of senescence-related substance, including H2O2 and MDA, and the activities of CAT, POD, and SOD in the third leaves of ZH8015 and es4 mutant, respectively. The results showed that content of H2O2 and MDA were remarkably higher in es4 leaves than that in ZH8015. The activities of CAT, POD and the content of SP were decreased in es4, while the activity of SOD increased in es4 mutant (Figures 3G–L). Therefore, the mutation of ES4 might lead to accumulation of H2O2.
Genetic Analysis, Mapping and Function Analysis of ES4
To isolate the premature leaf senescence gene responsible for the es4 mutant phenotype, we crossed the es4 mutant with 02428 to generate F1 population. All F1 individuals from the cross es4/02428 showed the normal green phenotype similar with ZH8015. In the F2 segregating population, 1634 normal plants and 580 early senescent plants showed a typical segregation ratio of 3:1(x2= 1.69 < x20.05 = 3.84, Supplementary Table S1). These results suggested that the early senescence phenotype was controlled by a single recessive nuclear gene.
1061 early senescent plants in F2 were used to locate ES4 by map-based cloning. ES4 was primarily mapped in the region linked to markers RM17303 and RM17377 on the long arm of chromosome 4 and subsequently fine mapped between X4–6 and X4–12 with a 33.5 Kb physical distance (Figures 4A,B). Seven open reading frames were annotated in this region according to the Rice Genome Annotation Project3. The genome DNA sequencing analysis of the final region revealed eight bases deletion at position 636 to 643 bp in the first exon of the sixth ORF named LOC_Os04g47300 encoding a Calcium-dependent protein kinase (OsCPK12) (Figure 4E). The es4 mutation led to a frameshift mutation in the STKc_CAMK domain of LOC_Os04g47300 (Figures 4C,D).
Figure 4. Map-based cloning of es4. (A) Location of es4 on chromosome. (B) A total of 1061 mutant type F2 individuals were used for fine mapping. (C) Seven ORF were found. (D) ES4 gene structure and CRISPR/Cas9 site of es4-cas9. (E) Mutant site of es4 and CRISPR/Cas9 site of es4-cas9.
To confirm that the OsCPK12 mutant was indeed responsible for the es4 mutant phenotype, the complementary vector pCAMBIA1300-OsCPK12 was transformed into the es4 calli. All the transgenic plants (es4-COM) restored to the wild-type phenotype (Figure 5A), and content of chlorophyll a and b, the expression level of OsCPK12 and Pn were also restored to wild-type levels (Figures 5C–E). Furthermore, the CRISPR/cas9 vector Cas9/gRNA was constructed to knock out the ES4 gene. ES4-Cas9 had a cytosine insertion at position 548–549 bp (Figure 4E) and all the transgenic plants (ES4-Cas9) exhibited the premature senescence (Figure 5B). Content of chlorophyll a and b, the expression levels of OsCPK12 and Pn were significantly reduced compared with ZH8015 (Figures 5C–E). These results demonstrated that the frameshift mutation of OsCPK12 was responsible for premature senescence phenotype in es4.
Figure 5. Functional complementation and CRISPR/Cas9 knock-out of ES4. (A) Plant of ZH8015, es4, and es4-COM at the mature stage. (B) Plant of ZH8015, es4, and es4-cas9 at the mature stage. (C) OsCPK12 relative expression level in ZH8015, es4, es4-COM, and ES4-cas9. (D) Content of Chlorophyll a and b in flag leaf of ZH8015, es4, es4-COM, and ES4-cas9 at the tillering stage. (E) Net photosynthetic rate (Pn) in flag leaf of ZH8015, es4, es4-COM, and ES4-cas9 at 70 dps (mean ± SD, n = 3), Scale bar = 4 cm. Letters in the figure indicate the results of multiple comparison test, a,b,c indicate significant difference on 0.01 level.
Enhancement of Pn and Content of Chlorophylls in Overexpression Plants of OsCPK12
To further verify the function of OsCPK12, the overexpression plants (OEPs) were constructed (Figure 6A). We found that the expression level of OsCPK12 in the overexpression transgenic lines was approximately 1.83-fold higher than that in ZH8015 (Figure 6B). The Pn and content of chlorophyll a and b in ES4-OEP plants were also higher than that in wide-type plants (Figures 6C,D). Therefore, the overexpression of OsCPK12 might enhance the Pn and content of Chlorophyll a and b, and thus leading to the delay of the growth period in rice.
Figure 6. Phenotypic characteristics of ZH8015 and overexpression plants OEP-1, OEP-2, and OEP-3; the relative expression level of OsCPK12 in ZH8015 and overexpression plants OEP-1, OEP-2, and OEP-3; the content of Chlorophyll a and b and Pn. (A) Plant of ZH8015 and OsCPK12-OEP at 70 dps. content. (B) The expression of OsCPK12. (C) The content of Chlorophyll a and b. (D) Net photosynthetic rate (Pn) (mean ± SD, n = 3), scale bar = 4 cm. Letters in the figure indicate the results of multiple comparison test, a,b,c indicate significant difference on 0.05 level.
The Expression Pattern of ES4
To determine the expression pattern of ES4 in rice, qRT-PCR was conducted using ES4 specific primers. As expected, the expression level in leaves was much higher than any other organs because the senescence phenotype appeared on leaves mainly. The expression levels in stems and sheaths were also higher while the expression levels were much lower in roots and panicles. The results revealed that although ES4 was ubiquitously expressed in many organs, and it was mainly expressed in photosynthetic organs such as stems and sheaths, especially in leaves (Figure 7A).
Figure 7. qRT-PCR analysis of OsCPK12, some photosynthesis and chlorophyll synthesis related genes. (A) Expression levels of OsCPK12 in different organs. (B) Expression levels of photosynthesis related genes. (C) Expression levels of synthesis and degradation of chlorophyll related genes (mean ± SD, n = 3), ∗ significance at P < 0.05, ∗∗ extremely significance at P < 0.01.
Expression of Some Photosynthesis and Chlorophyll Synthesis Related Genes
To understand the molecular basis of early senescence and photosynthesis and synthesis in es4, the relative expression levels of photosynthesis and synthesis-associated genes including OsPsaA, OsPsbA, OsLhcb1, OsLhcb4, OsCab1, OsRbcl, Hema, GSA, Heme1, Chld, RpoB, DVR, SGR, Rccr1, NYC1, and NOL were examined in ZH8015 and es4 by qRT-PCR at 70 dps. The expression levels of synthesis related genes including Hema, Heme1, GSA, Chld, RpoA, and DVR (Goslings et al., 2004; Zhang et al., 2006; Wang et al., 2010; Wang and Deng, 2013; Ohmiya et al., 2014) were significantly down-regulated in es4 (Figure 7B) and the expression levels of chlorophyll degradation related genes including SGR, Rccr1, NYC1, and NOL (Jiang et al., 2007; Kusaba et al., 2007; Tang et al., 2011; Sakuraba et al., 2013) were significantly up-regulated in es4 (Figure 7A). Photosynthesis related genes including OsPsaA, OsPsbA, OsLhcb1, OsLhcb4, OsCab1, and OsRbcl (Caffarri et al., 2004; Mei et al., 2017) were significantly down-regulated in es4 (Figure 7C). The results indicated that the mutation of ES4 was responsible for the decline of photosynthetic ability and the content of chlorophylls in es4.
During the process of plant senescence, the leaves undergo a series of physical and physiological changes: the breakdown of chloroplasts, the degradation of chlorophyll and the change of leaves color from green to yellow, the decrease in content of proteins (soluble protein especially), rise in the content and activity of hydrolases, enhancement of the content of MDA, the decreased activities of free radicals and active oxygen scavenging enzymes (such as SOD, POD, and CAT), and cell death (Wittenbach, 1977; Hua and Wang, 2003). Senescence is also associated with an increased production of ROS such as H2O2, superoxide and toxic derivative hydroxyl radical (Van Breusegem and Dat, 2006). These toxic ROS can result in lipid peroxidation, cellular damage and cell death, and genetic evidence suggests that ROS as a signaling molecule plays a major role in the senescence process by genetically activating programmed pathways of gene expression (Foyer and Noctor, 2005). These studies have established some aging indicators and deepened our understanding of leaf senescent process. In this study, we isolated an es4 mutant from ZH8015 characterized by an early senescence phenotype. es4 exhibited the breakdown of chloroplasts, the reduction of chlorophyll content, photosynthetic rate and crop yield. The activities of CAT, POD and the level of SP in es4 were significantly lower than those of ZH8015, while the content of H2O2, Superoxide radicals and MDA were significantly higher than those of ZH8015. These results were consistent with those found in other early senescence mutants in rice. Therefore, es4 is determined an early senescence mutant. SOD, as a biocatalyst, plays an important role in the aging and defense process of plants by disproportionating O2⋅- into H2O2 and O2. In some previous studies the change of SOD activity is unstable. For example, during the senescence of three representative cold super rice varieties, the SOD activity firstly increased and then declined (Yin et al., 2009). Other studies showed the leaf senescence is relevant to the reduction of SOD activity (Hua and Wang, 2003). Some studies showed the activity of SOD was increased in the mutant with senescent phenotype such as spl32 (Sun et al., 2017). In our study, the activities of SOD in es4 were significantly increased. The difference in SOD activity may be related with different measurement period in different studies. Our samples were taken from ZH8015 and es4 at 70 dps. but during this period, the lower leaves of es4 became yellow. O2⋅- is a necessary production of photooxidation during leaf senescence, and O2⋅- increased sharply during this stage. However, SOD is one of the systems for scavenging O2⋅-. In this stage, SOD system was not destroyed totally, so the activity of SOD increased to remove the elevated O2⋅- content. As alternative explanations can be made for the accumulation of O2⋅-, the increased activity of SOD was still not enough to scavenge the sharply elevated O2⋅-. Therefore, the activity of SOD was significantly increased and content of O2⋅- was also increased in es4. The elevation of ROS (such as O2⋅- and H2O2)content further accelerated leaf senescence in es4.
Our results showed that the mutant of OsCPK12 was responsible for the leaf early senescence of es4. OsCPK12 encodes a Calcium-dependent protein kinase (CPK). CPKs participate in numerous aspects of plant growth and development; however, there are few reports about the functions of CPKs in the process of senescence. The transient expression of the constitutively active mutant of NtCDPK2, A CPK from tobacco, in Nicotiana benthamiana leaves induced ROS production, defense genes, and HR-like cell death against additional abiotic stresses (Kobayashi et al., 2007). Potato (Solanum tuberosum) calcium-dependent protein kinase (StCDPK5) has been shown to phosphorylate the N-terminal region of plasma membrane RBOH (respiratory burst oxidase homolog) protein and participate in StRBOHB-mediated ROS burst (Kobayashi et al., 2012). The expression of AtCPK1, a CPK gene in Arabidopsis, in Rubia cordifolia cells caused moderate and stable elevation of intracellular reactive oxygen species (ROS) levels (Bulgakov et al., 2011). Ectopic expression of OsCPK13 (OsCDPK7) in rice without abnormal phenotype led to improved abiotic stress tolerance (Saijo et al., 2001). Moreover, expression of the rice CDPK-7 in sorghum led to enhanced accumulation of cell death and PR proteins and elevated transcription level of some defense genes and induced a lesion mimic phenotype (Mall et al., 2011). These studies indicated that CPKs may involve in regulating senescence directly or indirectly by mediating the content of ABA and ROS in plants. OsCPK12 is a member of the CPKs family in rice with functions in multiple signaling pathways. Ye’s study indicated that the expression level of OsCPK12 was up-regulated in the endosperm stage (Ye et al., 2009). OsCPK12 also oppositely modulates salt-stress tolerance and blast disease resistance for the decrease of ROS content in overexpression of OsCPK12 plants (Asano et al., 2012). Besides, the Arabidopsis CPK12 was a negative ABA-signaling regulator in seed germination and post-germination growth (Zhao et al., 2011). OsCPK12 involved in the signal transduction pathways and the overexpression of OsCPK12 demonstrated increased ability to growth under low nitrogen conditions (Asano et al., 2012). OsCPK12 was involved in nitrogen metabolism and overexpression of OsCPK12 increased nitrogen-use efficiency, improving yields when little nitrogen was available (Xing et al., 2018). Xing’s studies have confirmed that OsCPK12 is indeed related to premature senescence of rice. Researchers cloned a gene namely ESL4 about rice leaf senescence which was the same as ES4. The esl4 mutant became yellow at the early tillering stage, and the senescent phenotype was developed gradually at an early stage of heading. Their results indicated OsCPK12 was involved in nitrogen metabolism thus resulted in leaf senescence (Xing et al., 2018). However, our study found that OsCPK12 was not only related with nitrogen metabolism but also related with chlorophyll metabolism and photosynthesis.
In our study, the Pn and content of Chlorophyll a and b in es4 and ES4-cas9 were significantly lower than those in ZH8015. In the complementary transgenic plants, Pn and content of Chlorophyll a and b were the same as those in ZH8015. The overexpression of OsCPK12 enhanced the Pn and content of chlorophylls in ES4-OEP plants. Overexpression of OsCPK12 in ZH8015 also resulted in a delayed leaf senescence. Compared with ZH8015, the expression levels of five photosynthesis related genes were down-regulated in es4; the expression levels of Chlorophyll synthesis related genes slightly down-regulated in es4 and the expression levels of Chlorophyll degradation related genes slightly up-regulated in es4. These findings suggested that the OsCPK12 also participates in both chlorophyll metabolism and photosynthesis. Previous studies have shown that chlorophyll content had a positive and significant correlation with yield in rice (Ghosh et al., 2003). Leaf photosynthesis in rice was also related to grain yield (Ishii, 1993). The grain yield of rice is directly determined by the number of panicles per plant, the number of grains per panicle, and grain weight (Huo et al., 2017). There was no significant difference in the number of panicles per plant between ZH8015 and es4, but the spikelet number per panicle, seed setting rate and 1000-grain weight of es4 were lower than those of ZH8015, which resulted in a poor yield in es4. Therefore, in our study, leaf photosynthesis and chlorophyll content also had a positive relation with grain yield. The mutant of OsCPK12 severely reduced rice yield. Taken together, our results showed that OsCPK12 function is multidimensional and that it plays a very important role in the process of growth and development.
In summary, the functional loss of OsCPK12 results in the changes in activities of CAT, POD, and SOD, accumulation of the ROS and MDA, reduction of Pn and chlorophyll content, which eventually leads to leaf senescence and reduced yields. These results suggest that OsCPK12 not only plays an important role in biotic and abiotic stress, nitrogen metabolism but also involves the process of leaf senescence in rice, and the overexpression of OsCPK12 might provide the potential raise on productivity in rice.
BW performed most of the research and drafted the manuscript. YZ designed the experiments. ZB carried out the nucleotide polymorphism analysis. QL, TX, NY, YC, and AZ analyzed the data. QL, TX, WW, XZ, GA, PY, and DC revised the manuscript. SC and LC supervised the study and revised the manuscript. All authors read and approved the final manuscript.
This study was financed by Technological Innovation Project of CAAS, study on the mechanism of heterosis in rice (CAAS-ASTIP-2013-CNRRI), Major Projects of Genetically Modified, Breeding of New Disease-resistant Transgenic Rice Varieties (2016ZX08001-002), and National Natural Science Foundation of China (31521064).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2019.00052/full#supplementary-material
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Keywords: rice (Oryza sativa L.), early senescence, es4, OsCPK12, calcium-dependent protein kinase
Citation: Wang B, Zhang Y, Bi Z, Liu Q, Xu T, Yu N, Cao Y, Zhu A, Wu W, Zhan X, Anis GB, Yu P, Chen D, Cheng S and Cao L (2019) Impaired Function of the Calcium-Dependent Protein Kinase, OsCPK12, Leads to Early Senescence in Rice (Oryza sativa L.). Front. Plant Sci. 10:52. doi: 10.3389/fpls.2019.00052
Received: 30 October 2018; Accepted: 16 January 2019;
Published: 04 February 2019.
Edited by:Michael J. Haydon, The University of Melbourne, Australia
Reviewed by:Wenchao Huang, Wuhan University, China
Zhaowei Li, Fujian Agriculture and Forestry University, China
Copyright © 2019 Wang, Zhang, Bi, Liu, Xu, Yu, Cao, Zhu, Wu, Zhan, Anis, Yu, Chen, Cheng and Cao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
†These authors have contributed equally to this work