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Overexpression of rice jacalin-related mannose-binding lectin (OsJAC1) enhances resistance to ionizing radiation in Arabidopsis



Jacalin-related lectins in plants are important in defense signaling and regulate growth, development, and response to abiotic stress. We characterized the function of a rice mannose-binding jacalin-related lectin (OsJAC1) in the response to DNA damage from gamma radiation.


Time- and dose-dependent changes of OsJAC1 expression in rice were detected in response to gamma radiation. To identify OsJAC1 function, OsJAC1-overexpressing transgenic Arabidopsis plants were generated. Interestingly, OsJAC1 overexpression conferred hyper-resistance to gamma radiation in these plants. Using comparative transcriptome analysis, genes related to pathogen defense were identified among 22 differentially expressed genes in OsJAC1-overexpressing Arabidopsis lines following gamma irradiation. Furthermore, expression profiles of genes associated with the plant response to DNA damage were determined in these transgenic lines, revealing expression changes of important DNA damage checkpoint and perception regulatory components, namely MCMs, RPA, ATM, and MRE11.


OsJAC1 overexpression may confer hyper-resistance to gamma radiation via activation of DNA damage perception and DNA damage checkpoints in Arabidopsis, implicating OsJAC1 as a key player in DNA damage response in plants. This study is the first report of a role for mannose-binding jacalin-related lectin in DNA damage.


Lectins are carbohydrate-binding proteins that play diverse roles in both plants and animals [1]. In plants, lectins interact with endogenous carbohydrates and reportedly are involved in signaling pathways [2]. Twelve subfamilies of plant lectins have been identified [3]. One subfamily, the jacalin-related lectins (JRLs), is named for the presence of a jacalin-like domain and comprises 25 identified members [4]. This large subfamily has been further divided into two subgroups, based on the members’ carbohydrate-binding properties, subcellular localization, and molecular structures [5]. For example, mannose-binding JRLs are located in both the nucleus and the cytosol, whereas galactose-binding JRLs are located in vascular compartments [5]. Plant JRLs are important in the response to biotic stresses, such as pathogen and insect attack [6], as well as abiotic stresses, such as salinity stress [7]. Functionally, most JRLs are related to disease resistance and signaling in response to multiples stresses [8]. Particularly, JRLs with dirigent domains have been associated with plant defenses to pathogens. OsJAC1 is a mannose-binding JRL from rice (Oryza sativa). This factor contains a dirigent domain in its N-terminal region as described by Jiang et al. [9]. Overexpression of OsJAC1 suppressed elongation of coleoptiles and internodes, consistent with a regulatory function for OsJAC1 in growth and development [10]. Furthermore, Weidenbach et al. [11] concluded that this protein is also involved in plant defense to pathogen attack.

The genomes of all organisms are vulnerable to a variety of detrimental endogenous and exogenous factors, including replication errors, reactive oxygen species (ROS), ionizing radiation, and genotoxic chemicals. Ionizing radiation, which includes gamma radiation, is a carcinogen. Gamma irradiation directly damages a genome by introducing double-strand breaks (DSBs) in the DNA [12]. Repair of DSBs occurs via two important pathways: non-homologous end joining and homologous recombination [13]. In addition, gamma radiation also indirectly induces DNA damage via the generation of ROS, which introduces different types of DNA lesions [14]. Cellular DNA damage response (DDR) mechanisms, including repair mechanisms, to maintain genomic integrity, are fundamentally conserved across all organisms [15, 16]. One important regulator of DDR is ataxia telangiectasia mutated (ATM) protein [17], which is a signal transducer that acts in response to DSBs. Ataxia telangiectasia and RAD3-related (ATR) protein is also involved in signaling in response to single-strand breaks and stalled replication forks [18].

DNA replication is important for transmission of genetic information to daughter cells and progeny; therefore, all organisms have mechanisms to protect the fidelity of DNA replication. For example, DNA damage can adversely affect the replication machinery and result in a stalled replication fork. DNA replication is initiated at numerous origins of replication in eukaryotes [19] via a two-step process. The first step is origin licensing, which starts with a pre-replicative complex in late mitosis or the G1 phase of the cell cycle [20]. The pre-replicative complex is composed of cell division 6 (CDC6), the origin-recognition complex, the cell division cycle 10-dependent transcript 1 (Cdt1), and mini-chromosome maintenance proteins 2–7 (MCM2-MCM7). The second step, origin firing, begins with activation of the MCM2–7 complex. Component kinases, such as cycle dependent kinase (CDK) and Dbf-dependent kinase (DDK), that are specific to the S phase of the cell cycle are required for this origin firing step [20, 21].

In our preliminary microarray studies, differential expression of OsJAC1 was found in response to ionizing radiation (unpublished data). Several studies reported that plant JRLs are involved in responses to abiotic and biotic stress [6,7,8]; however, no evidence for a role of JRLs in DDR has been published. Therefore, we examined the molecular function of OsJAC1 in DDR. We sought to establish the effect of ionizing radiation and abiotic stresses on the expression of OsJAC1. We also generated transgenic OsJAC1-overexpressing Arabidopsis lines that were resistant to gamma irradiation. We probed the molecular mechanism underlying OsJAC1 function on DDR using comparative transcriptome analysis of the OsJAC1-overexpressing lines.


Expression analysis of OsJAC1 in rice plants in response to ionizing radiation, abiotic stresses, and plant hormones

We measured OsJAC1 expression over time in 2-week-old seedlings after exposure to different dosages of gamma radiation. OsJAC1 expression was greatly reduced in rice seedlings immediately after exposure at all levels of irradiation tested (Fig. 1a). Compared to untreated controls, the numbers of OsJAC1 transcripts were reduced approximately 150- and 50-fold in plants exposed to 100 and 300 Gy gamma irradiation, respectively. The transcript levels were slightly increased 6, 12, and 24 h after irradiation compared to the 0-h time point (Fig. 1b-d); however, by 48 h after irradiation, we observed a greater than 2-fold induction of OsJAC1 expression in seedlings compared to levels in a non-irradiated control (Fig. 1e). Furthermore, the numbers of transcripts were increased at all doses of irradiation at 168 h (corresponding to 7 d) compared to the unirradiated control. These increases were approximately 30-, 4-, and 8-fold at 100, 200, and 300 Gy of gamma irradiation, respectively (Fig. 1f). To confirm this late induction of OsJAC1 transcript expression in response to ionizing radiation, dry rice seeds were irradiated with gamma radiation or an ion beam, subsequently germinated on MS media, and irradiated after 2 weeks. These seedlings exhibited increased OsJAC1 transcripts in response to both types of radiation (Fig. 1g, h).

Fig. 1
figure 1

Expression of OsJAC1 in rice seedlings irradiated with ionizing radiation as determined with quantitative RT-PCR. a-f: Time courses of expression of OsJAC1 in 2-week-old rice seedlings after exposure to the indicated levels of gamma radiation. g, h: Expression of OsJAC1 in 2-week-old seedlings from rice seeds that had been irradiated with gamma radiation (g) or with an ion beam (h) and then germinated on MS media. Values represent means ± SD (n = 3). Statistical analysis was carried out by one-way ANOVA (*p < 0.01)

Additionally, OsJAC1 expression was altered by exposure to other stressors. OsJAC1 expression was also upregulated in response to salinity stress (Fig. 2a). In seedlings treated with NaCl for 6 h, we observed an approximately 8-fold increase in the number of OsJAC1 transcripts compared to untreated seedlings. The OsJAC1 transcript expression was also slightly increased after 3 h of exposure to heat stress, although no significant difference was observed after 6 or 12 h of exposure (Fig. 2b). Expression levels of OsJAC1 were also upregulated by jasmonic acid (JA) and salicylic acid (SA) treatment (Fig. 2c, d). OsJAC1 expression was approximately 40-fold higher 12 h after JA treatment, while SA treatment resulted in a 5-fold induction of OsJAC1 expression at this time point compared with levels in the untreated control.

Fig. 2
figure 2

Time course of expression of OsJAC1 in 2-week-old rice seedlings exposed to abiotic stresses (a) salinity stress or (b) heat stress or to plant hormones (c) SA or (d) JA as determined by quantitative RT-PCR. Data represent means ± SD (n = 3). One-way ANOVA was used for statistical analysis (**p < 0.01, 0.01 < *p < 0.05)

Generation of Arabidopsis OsJAC1-overexpressing lines

We next sought to probe the molecular function of OsJAC1 by generating OsJAC1-overexpressing Arabidopsis lines. A schematic diagram (Fig. 3a) shows the structure of the OsJAC1-overexpressing construct in which OsJAC1 is regulated by the 35S promoter and terminator. Two transgenic lines, #16–6 and #18–2, displayed significant overexpression, approximately 70- and 130-fold, respectively (Fig. 3b). OsJAC1 overexpression was accompanied by higher levels of OsJAC1 protein in both transgenic lines than in a wild-type control (Fig. 3c). Figure 3d displays the morphology of the transgenic lines in the early vegetative growth stage, revealing no obvious morphological differences in the transgenic lines in comparison to a wild-type control in the absence of exposure to radiation.

Fig. 3
figure 3

Generation of OsJAC1-overexpressing Arabidopsis lines and confirmation of enhanced expression. a Schematic diagram of vector construct for OsJAC1 overexpression. b OsJAC1 transcripts in OsJAC1-overexpressing lines were detected using quantitative RT-PCR. Data represent means ± SD (n = 3). Statistical analysis was carried out by one-way ANOVA (*p < 0.01). c Expression levels of OsJAC1 in OsJAC1-overexpressing lines as determined using western blot. d Photographs of OsJAC1-overexpressing lines and wild-type plants 30 d after sowing. Note that morphologies are similar

OsJAC1 overexpression leads to hyper-resistance to gamma radiation

We then assessed the effect of OsJAC1 overexpression on growth and development in response to gamma radiation. Transgenic lines and wild-type control plants were irradiated with 200 or 300 Gy gamma radiation, and growth rates were compared 2 weeks later. There were no morphological differences between the transgenic and control plants in the reproductive stage in the absence of irradiation (Fig. 4a). Following irradiation, the OsJAC1-overexpressing lines grew faster than wild-type plants at both doses of irradiation (Fig. 4a). Consequently, the overexpressing lines were taller and accumulated more mass than the irradiated control plants (Fig. 4b, c). Specifically, both OsJAC1-overexpressing lines displayed plant heights and fresh weights that were more than 3-fold higher than those in controls after treatment with 300 Gy gamma radiation. We also measured the growth rates of OsJAC1-overexpressing lines treated with NaCl as a means to impose salinity stress. OsJAC1 overexpression enhanced root growth in the stressed plants compared to unstressed plants (Additional file 1: Figure S1). Therefore, we conclude that plants with OsJAC1 overexpression possess resistances to both gamma radiation and salinity stress.

Fig. 4
figure 4

Morphological features and growth responses of OsJAC1-overexpressing Arabidopsis lines in response to gamma radiation. a Two-week-old seedlings were irradiated using gamma radiation. Photographs of OsJAC1-overexpressing lines and wild-type plants 30 d after irradiation. b, c Heights and fresh weights of OsJAC1-overexpressing lines and wild-type plants after gamma irradiation. Data represent means ± SD (n = 3). Statistical analysis was carried out by one-way ANOVA (**p < 0.01, 0.01 < *p < 0.05)

Transcriptomic analysis of the DNA damage response in OsJAC1-overexpressing lines

Our next step was to probe the molecular function of OsJAC1 in DDR. We performed transcriptome analysis of OsJAC1-overexpressing lines. A total of more than 129 million trimmed reads were generated from a wild-type control and two OsJAC1-overexpressing transgenic lines treated with or without gamma irradiation (Table 1). Trimmed reads were mapped to the reference gene set from the ARAPORT database ( The average mapped rate of six samples was 84% (Table 1). Figure 5 shows the number of upregulated and downregulated DEGs in both OsJAC1-overexpressing lines compared to the wild-type control after 100 Gy gamma irradiation. The two transgenic lines shared 12 upregulated and 10 downregulated DEGs. In upregulated DEGs, three xyloglucan endotransglucosylase/hydrolase genes (AT4G14130, AT3G23730, and AT5G65730) were detected (Table 2). Interestingly, pathogen defense-related genes, such as disease resistance proteins (AT5G41740 and AT5G41750) and NPR1-like protein (AT5G45110), were among the downregulated DEGs of both OsJAC1-overexpressing lines. Additional file 2: Table S1 shows expression data for all annotated transcripts in OsJAC1-overexpressing lines..

Table 1 Number of trimmed and mapped reads of wild-type and OsJAC1-overexpressing transgenic lines with/without gamma irradiation
Fig. 5
figure 5

DEG analysis of OsJAC1-overexpressing Arabidopsis lines compared to a wild-type control after 100 Gy gamma irradiation. Venn diagrams show number of upregulated (a) and downregulated (b) DEGs

Table 2 Up- and down-regulated DEGs were commonly detected in both OsJAC1-overexpressing lines

We next assessed the expression profile of genes involved in DNA replication in OsJAC1-overexpressing lines with and without gamma irradiation (Fig. 6). In the absence of irradiation, expression of MCM5, 6, and 7 was greater in OsJAC1-overexpressing lines than in the wild-type control. Following irradiation, the expression of MCM6 and MCM7 was significantly upregulated in OsJAC1-overexpressing lines compared to the irradiated control plant.

Fig. 6
figure 6

Comparative transcriptome expression profiles of genes involved in DNA replication from OsJAC1-overexpressing lines and a wild-type control before and after gamma irradiation

Additionally, the transcript level of At1g23750 (replication protein A1) was significantly reduced by OsJAC1 overexpression in the absence of irradiation compared to the wild-type control. There were fewer RPA3A and RPA3B transcripts in OsJAC1-overexpressing lines without gamma irradiation compared to the wild-type control, whereas gamma irradiation resulted in transcriptional induction of these two genes (Fig. 6). Both POLGAMMA1 and the At5g67100 (DNA polymerase alpha subunit A) gene were upregulated in the transgenic lines in the absence of irradiation compared to the wild-type plants. Similarly, the expression levels of polymerase epsilon subunits TIL1 and TIL2 were increased by OsJAC1 overexpression under non-irradiated conditions, whereas slight reductions of these transcripts were observed after gamma irradiation. In addition, gamma irradiation resulted in transcriptional induction of the At1g67320 (DNA primase large subunit) gene in the transgenic lines (Fig. 6).

Figure 7 displays the expression levels of genes involved in homologous recombination repair. OsJAC1 overexpression affected the accumulation of ATM. Expression of this gene was significantly upregulated in non-irradiated OsJAC1-overexpressing lines compared to the wild-type control. Interestingly, we did not detect significant differences in ATR expression between the overexpressing lines and the wild-type control (data not shown). Meiotic recombination 11 (MRE11) and Fanconi anemia group J protein were upregulated by OsJAC1 overexpression in both irradiated and non-irradiated plants (Fig. 7).

Fig. 7
figure 7

Comparative transcriptome expression profiles of genes associated with homologous recombination from OsJAC1-overexpressing lines and a wild-type control with and without gamma irradiation

Figure 8 shows the expression patterns of genes related to nucleotide excision repair, mismatch repair, and non-homologous recombination. In nucleotide excision repair, OsJAC1 overexpression enhanced the transcriptional accumulation of DDB1A and DDB1B (UV-damaged DNA damage-binding proteins) under non-irradiated conditions (Fig. 8a). DNA mismatch repair genes MSH3, MSH6, and MLH3 were increased in both transgenic lines (Fig. 8b), and gene expression of the non-homologous recombination repair factor At4G57160 (DNA ligase 4) was increased by OsJAC1 overexpression without gamma irradiation (Fig. 8c).

Fig. 8
figure 8

Comparative transcriptome expression profiles for genes related to (a) nucleotide excision repair, (b) mismatch repair, and (c) non-homologous recombination repair from OsJAC1-overexpressing lines and a wild-type control before and after gamma irradiation


OsJAC1 is involved in the response to abiotic stress, including gamma irradiation and salinity stress

JRLs are associated with plant responses to stress, including abiotic stresses and attack by pathogens [8]. The expression of OsJAC1, which encodes a JRL, was upregulated in a time- and dose-dependent manner following exposure to both gamma radiation and an ion beam (Fig. 1). We noted some similarities between these responses and two relevant previous studies. Jin et al. [22], using microarray analysis, observed time- and dose-dependent expression of genes associated with signal transduction, transcription, and metabolism in human mesenchymal stem cells exposed to gamma radiation. These genes were either involved in cellular defense, such as apoptosis and responses to stress, or in fundamental cellular processes, such as DNA replication and repair. It has been also been noted that in Chlamydomonas reinhardtii [23], the expression of many DDR genes was altered by gamma irradiation. From the similarities between the response of OsJAC1 and these other genes to radiation, we hypothesized that OsJAC1 may participate in DDR, perhaps in signal transduction involved in these processes.

Given the central role of JRLs in the response of plants to stress, we also examined the response of OsJAC1 expression to salinity stress. Salinity stress, like irradiation, increased OsJAC1 expression in rice (Fig. 2a), and OsJAC1-overexpressing lines displayed resistance to salinity stress compared to a wild-type control (Additional file 1: Figure S1). Similar observations were made by Zhang et al. [7], who also identified a relationship between lectins and abiotic stresses, including salinity stress, in rice. One effect of salinity stress in plants is the generation of ROS [24], which are also generated by ionizing radiation. ROS damages cellular components, including DNA, in numerous ways [25, 26], and these similar responses further strengthen the relationship between OsJAC1 and DDR.

JRLs are regulated by the plant hormones JA and SA, which are related to stress responses and pathogen defense in plants [11, 27, 28]. Thus, we examined the effect of these hormones on expression of OsJAC1. The hormones enhanced transcription of OsJAC1 (Fig. 2c, d). SA is associated with genotoxic stress that results from exposure to ethyl methanesulphonate and methyl mercuric chloride [29] and may enhance the genotoxic stress-related signaling pathway [30]; however, the role of SA in this signaling remains unclear [31]. These hormones play central roles in the plant defense response to ROS [32, 33], and their signaling pathways were affected in a dose-dependent manner by H2O2 accumulation in the cat2 Arabidopsis mutant [34, 35]. Similarly, silencing of mannose-binding lectin (CaMLB1) transcript led to a reduction in both disease resistance and ROS accumulation in pepper plants [36]. Furthermore, Weidenbach et al. [11] reported that OsJAC1 mediated the pathogen defense response in rice. Interestingly, however, DEG analysis displayed downregulation of pathogen defense-related genes in OsJAC1-overexpressing lines (Table 2). These results suggest that OsJAC1 regulates different stresses, such as DNA damage and pathogen attack, via coordination with levels of ROS in plants.

OsJAC1 overaccumulation leads to modulation of DNA replication components

The relationship between OsJAC1 and abiotic stresses is well documented [7], but the molecular function of this protein has not been established. We first probed the molecular function of OsJAC1 in DDR following exposure of plants to gamma radiation. Arabidopsis lines overexpressing OsJAC1 showed tolerance to gamma radiation (Fig. 4). In addition, DEG analysis revealed that these transgenic lines highlighted differential expression of genes involved in pathogen defense after gamma irradiation (Fig. 5 and Table 2). OsJAC1 functions in pathogen defense have been well characterized previously [11]. Hadwiger et al. [37] also reported that DDR is closely associated with pathogen defense via SA signaling. Thus, differential expression of pathogen-related genes in response to gamma radiation in OsJAC1-overexpressing lines indicates that OsJAC1 may function in the overlapping pathways between DDR and pathogen defense.

DDR serves as a regulation signal for many DNA repair pathways, which have presumably evolved to maintain genome integrity. DDR also regulates apoptosis, senescence, and the DNA replication process [38]. DNA replication is a key step for cell proliferation, because genome duplication for transmission is essential in all organisms. Figure 6 shows the expression levels of genes associated with DNA replication in OsJAC1-overexpressing lines. It is of particular interest that the transcript numbers of MCM4-MCM7 were increased in OsJAC1-overexpressing lines. MCM proteins are licensing factors for DNA replication [39]. For formation of the pre-replicative complex, MCMs form a complex with OCR, CDT1, and CDC6/CDC18 [40,41,42]. MCM genes have been identified in A. thaliana, Zea mays, and O. sativa and are expressed in young tissues with replicating cells [39, 43]. We observed significant accumulation of MCM6 transcripts after exposure to gamma radiation in OsJAC1-overexpressing lines (Fig. 6). Dang et al. [44] noted that the MCM6 single subunit was essential in abiotic stress tolerance in plants. Upregulation of MCM6 was detected in pea plants exposed to salinity and cold stresses, and overexpression of pea MCM6 in tobacco conferred resistance to salinity stress. Therefore, upregulation of MCM transcripts by OsJAC1 overexpression indicates that OsJAC1 may participate in the regulation of DNA replication stresses induced by salt and gamma radiation.

RPA, which is a single-strand DNA-binding protein that is composed of three subunits (RPA1, 2, 3) is associated with DNA repair, meiosis, and DNA replication and activates cellular responses to DNA damage [45]. Low levels of RPA3A and RPA3B transcripts were detected in OsJAC1-overexpressing lines before irradiation compared to a wild-type control, but gamma irradiation increased the numbers of these RPA transcripts (Fig. 6). DNA polymerase epsilon is composed of four subunits: one large subunit TILl (Pol2) and three small subunits, DNA-binding protein (DPB) 2, 3, and 4 [46]. The exact functions of polymerase delta and epsilon remain controversial, but polymerase epsilon is associated with replicative error repair and replicative stress sensing [47, 48]. In OsJAC1-overexpressing lines, TIL1 and TIL2 were upregulated compared to levels in wild-type plants, but genes for both subunits were slightly downregulated following gamma irradiation compared to the levels before irradiation (Fig. 6). Arabidopsis mutant abo4–1, which has a partially defective polymerase epsilon subunit, was resistant to replicative stress but hypersensitive to DNA damaging agents, including zeiocin [48, 49]. Furthermore, overexpression of polymerase epsilon small subunit DPB2 impaired DNA replication in Arabidopsis. Thus, we conclude that OsJAC1 overexpression altered expression of genes involved in DNA replication, implicating OsJAC1 function in DNA replication.

OsJAC1 may coordinate with MRE11 and ATM to enhance DNA repair

Cellular response to DNA damage is regulated the protein kinases ATM and ATR, which are activated by different types of DNA damage [50,51,52]. ATM is mainly activated in response to DSBs, while ATR is activated in response to stalled replication forks. Canman et al. [53] observed ATM activation in response to DSB-inducing ionizing radiation in mammalian cells. In the present study, OsJAC1-overexpressing lines exhibited greater ATM transcript expression than the wild-type control in the absence of irradiation (Fig. 7), while no difference in the numbers of ATR transcripts were observed between the transgenic lines and a control (data not shown). We also observed increased MRE11 expression in OsJAC1-overexpressing lines compared to the wild-type control (Fig. 7). MRE11 is a component of the MRN complex, which includes radiation sensitive 50 (RAD50) and Nijmegen breakage syndrome 1 (NBS1) and serves as the sensor of DSBs. This complex is also important in DNA damage repair, DNA replication, meiosis, and genome stability [54]. Following binding to DSBs, the MRN complex activates ATM [55, 56], but this complex is not required for ATR activation [57]. Interactions between MRE11 and DNA replication have been noted. Specifically, MRE11 is necessary for the recovery of hydroxyurea-induced replication stress in HeLa cells, and the MRN complex and RPA co-localized and interacted following treatment with either hydroxyurea or UV light [58]. Taken together, these results suggest that OsJAC1 regulates DNA damage perception and DNA repair as well as in DNA replication via coordination with ATM and MRE11.

Furthermore, we examined the role of OsJAC1 in nucleotide excision repair. The UV-damage DNA-binding protein complex was first reported in human cells. Overexpression of DDB1A and DDB1B enhanced resistance to UV radiation in Arabidopsis, whereas two knock-out mutants, ddb1a and ddb1b, were susceptible [59, 60]. Our results are consistent with this previous report, as DDB1A and DDB1B transcripts in OsJAC1-overexpressing transgenic lines were increased (Fig. 8a). Mismatched nucleotide bases that result from insertion, deletion and mis-incorporation lead to polymerase mis-incorporation and incorrect recombination of DNA. DNA mismatch repair (MMR) systems detect and repair these mismatched nucleotides, and Mut genes play important roles in genome maintenance [61]. MSH (MutS homologs) and MHL (MutL homologs) are highly conserved proteins; although, these factors have diverse cellular functions [62]. In the present study, Arabidopsis lines overexpressing OsJAC1 had greater expression of MSH3, MSH6, and MHL3 transcripts than the wild-type control (Fig. 8b). Previously, MSH2-deficient mouse cells were found to have low survival rates after X-ray irradiation, and MSH2 required re-localization of RAD51 and MRE11 in the G2 phase of the cell cycle [63]. Together, these results may indicate that OsJAC1 is linked with both MMR and NER in the DDR pathway.


Figure 9 displays a scheme illustrating the hyper-resistance to ionizing radiation conferred by OsJAC1 overexpression. In summary, we suggest that the observed upregulation of ATM and MRE11 by OsJAC1 overexpression provides evidence of enhanced DNA damage perception. We interpret the observed transcriptional changes of genes encoding DNA polymerases, RPAs, and MCMs as evidence for the activation of DNA damage checkpoints in response to replication stress in OsJAC1-overexpressing lines. Thus, activation of both DNA damage perception and DNA damage checkpoints by OsJAC1 overexpression may confer hyper-resistance to gamma radiation in Arabidopsis.

Fig. 9
figure 9

Scheme of the involvement of OsJAC1 in the DDR pathway. Dotted lines indicate possible regulation or transcriptional coordination of the pathway by OsJAC1


Plant growth conditions

Oryza sativa spp. japonica cv. Ilpoom was obtained from the Rural Development Administration of Korea. Arabidopsis thaliana ecotype Landsberg erecta, originated from the Arabidopsis Biological Resource Center, was acquired from Kumho Life Science Laboratory of Chonnam National University in Korea. Rice plants were grown at 30 °C with a cycle of 16 h light followed by 8 h dark. Arabidopsis plants were cultured at 23 °C under the light and dark cycle as described above.

Generation of OsJAC1-overexpressing Arabidopsis lines

OsJAC1 (XM_015763269) cDNA was amplified with gene-specific primers using the polymerase chain reaction (PCR). The PCR conditions were as follows: one cycle at 94 °C for 5 min; 35 cycles at 92 °C for 1 min, 57 °C for 1 min, and 72 °C for 1 min; and one cycle at 72 °C for 5 min. Primer sequences for OsJAC1 were 5′-ATG GCT GAT CCC AGC AAG CTG CA-3′ and 5′-TTA GAT CGG CTG CAC GTA GAC ACC AAC-3′. The amplified OsJAC1 cDNA was sub-cloned into the pCR™8/GW/TOPO® vector and then transferred into the pMDC83 vector using the Gateway cloning system according to the manufacturer’s instructions. The OsJAC1-overexpressing construct was introduced into Agrobacterium tumefaciens LBA4404 using electroporation. Arabidopsis plants were transformed using the floral dip method [64]. Seeds were harvested from the dipped Arabidopsis plants. To identify insertion of the OsJAC1-overexpressing construct, selection was performed using MS media containing 50 μg/ml kanamycin. To obtain homozygous OsJAC1-overexpressing lines, segregation analyses of seeds from the selected progenies were carried out. Six homozygous lines with OsJAC1 overexpression were identified.

Conditions of gamma irradiation

Rice seeds were germinated on Murashige and Skoog (MS; Duechefa, Haarlem, Netherlands) solid media containing 0.8% agar and 1% sucrose. Two-week-old seedlings were irradiated with gamma radiation using a gamma irradiator (60Co, approximately 150 TBq; Atomic Energy of Canada, Ltd., Ottawa, Ontario) for 12 h at the Korea Atomic Energy Research Institute. To identify dose-dependent effects, various doses (100, 200, 300, and 400 Gy) of gamma radiation were used for each sample. Seedling samples were obtained at different times (0–168 h) after gamma irradiation for analysis. For confirmation of time-dependent expression of OsJAC1 in response to ionizing radiation, dry rice seeds were exposed to gamma radiation at different doses (100, 200, 300, and 400 Gy), and then seeds were germinated on MS media. Two-week-old rice seedlings were harvested.

Imposition of salinity stress and treatment with plant hormones

For plant hormone treatment, rice seeds were germinated in MS solid media containing 0.8% agar and 1% sucrose. Two-week-old rice seedlings were treated with 1 mM SA (Sigma, St. Louis, MO, USA) and 0.1 mM JA (Sigma). Samples were collected at 6, 12, and 24 h after each treatment. For imposition of heat stress, 2-week-old rice seedlings were incubated at 45 °C for 2 h. Samples were obtained 0, 3, 6, and 12 h after heat treatment.

RNA isolation and quantitative reverse transcription (RT)-PCR

Total RNA was isolated using RNeasy plant mini kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions, and then DNA contamination was removed using RNase-free DNase (Takara, Kyoto, Japan). The cDNA synthesis was performed using the Superscript®III reverse transcriptase (Invitrogen, Carlsbad, CA, USA). For quantitative RT-PCR, cDNA amplification was performed using Power SYBR Green PCR master mix (Thermo Fisher Scientific, Rockford, IL, USA) with the CFX™ Real-Time System (Bio-Rad, Hercules, CA, USA). Conditions for the PCR reactions were as follows: one cycle at 94 °C for 5 min; 40 cycles at 92 °C for 30 s, 60 °C for 30 s, and 72 °C for 30 s; one cycle at 72 °C for 5 min. Primer sequences for OsJAC1 were 5′-CGT CTC GAA AGC ATC ACA TT-3′ and 5′-CGG CAT GGT CAA GGT AAG TA-3′ and for Actin were 5′-TGA AGT GCG ACG TGG ATA TTA G-3′ and 5′-CAG TGA TCT CCT TGC TCA-3′.

Western blot analysis

For total protein extraction, whole plant tissues were homogenized in extraction buffer (100 mM Tris-Cl, pH 7.5; 1 mM ethylenediaminstetraacetic acid; 0.5 NP-40; 150 mM NaCl; 3 mM dithiothreitol) and protease inhibitor (Sigma). Total proteins were separated on a sodium dodecyl sulfate-polyacrylamide gel (Sigma) by electrophoresis and then transferred onto Immobilon-P membranes (Millipore, Burlington, MA, USA). Immunodetection was performed with a rat anti-GFP antibody (Abcam, Cambridge, MA, USA) and visualized using a chemiluminescence ECL kit (Thermo Fisher Science, Waltham, MA, USA) according to the manufacturer’s instruction.

Comparative transcriptome analysis

Two biological plant sample replicates were prepared for transcriptome analysis. RNA isolation was performed as described above. Transcriptome analysis was conducted as described by Koo et al. [65]. Briefly, mRNA-Seq paired-end libraries were constructed using the Illumina TruSeq RNA Sample Preparation Kit v2 (Illumina, San Diego, CA, USA), and the KAPA library quantification kit (Kapa Biosystems, Wilmington, MA, USA) was utilized for quantification of the library according to the manufacturer’s instruction. The cDNA libraries were sequenced using an Illumina HiSeq2000 (Illumina). For short-read mapping, reads were mapped to reference transcripts using the bowtie software (Langmead et al., 2009). DEGs (p ≤ 0.01 and fold-change ≥2) commonly expressed between the transgenic lines in comparison with the control were selected from the mapped reads.

Statistical analyses

One-way analyses (ANOVA) were performed for statistical analyses of quantitative RT-PCR and plant growth measurement using R program (version 3.6.1).

Availability of data and materials

All materials in the current article are available from the corresponding author.



Ataxia Telangiectasia Mutated protein


DNA damage response


Differentially expressed genes


Double-strand breaks


Rice mannose-binding jacalin-related lectin


  1. Peumans WJ, Van Damme EJ. Lectins as plant defense proteins. Plant Physiol. 1995;109:347–52.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Van Damme EJ, Barre A, Rouge P, Peumans WJ. Cytoplasmic/nuclear plant lectins: a new story. Trends Plant Sci. 2004;9(10):484–9.

    Article  PubMed  CAS  Google Scholar 

  3. Jiang SY, Ma Z, Ramachandran S. Evolutionary history and stress regulation of the lectin superfamily in higher plants. BMC Evol Biol. 2010;10:79.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  4. Y-j H, Z-h Z, L-l S, Olsson S, Wang ZH, Lu GD. Evolutionary analysis of plant jacalin-related lectins (JRLs) family and expression of rice JRLs in response to Magnaporthe oryzae. J Integr Agric. 2018;17:1252–66.

    Article  Google Scholar 

  5. Lannoo N, Van Damme EJ. Lectin domains at the frontiers of plant defense. Front Plant Sci. 2014;5:397.

    PubMed  PubMed Central  Google Scholar 

  6. Chrispeels MJ, Raikhel NV. Lectins, lectin genes, and their role in plant defense. Plant Cell. 1991;3:1–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  7. Zhang W, Peumans WJ, Barre A, Astoul CH, Rovira P, Rouge P, Proost P, Truffa-Bachi P, Jalali AA, Van Damme EJ. Isolation and characterization of a jacalin-related mannose-binding lectin from salt-stressed rice (Oryza sativa) plants. Planta. 2000;210(6):970–8.

    Article  CAS  PubMed  Google Scholar 

  8. Song M, Xu W, Xiang Y, Jia H, Zhang L, Ma Z. Association of jacalin-related lectins with wheat responses to stresses revealed by transcriptional profiling. Plant Mol Biol. 2014;84:95-110.

    Article  CAS  Google Scholar 

  9. Jiang JF, Han Y, Xing LJ, Xu YY, Xu ZH, Chong K. Cloning and expression of a novel cDNA encoding a mannose-specific jacalin-related lectin from Oryza sativa. Toxicon. 2006;47(1):133–9.

    Article  CAS  PubMed  Google Scholar 

  10. Jiang J-F, Xu Y-Y, Chong K. Overexpression of OsJAC1, a Lectin gene, suppresses the coleoptile and stem elongation in Rice. J Integr Plant Biol. 2007;49:230–7.

    Article  CAS  Google Scholar 

  11. Weidenbach D, Esch L, Moller C, Hensel G, Kumlehn J, Hofle C, Huckelhoven R, Schaffrath U. Polarized defense against fungal pathogens is mediated by the Jacalin-related Lectin domain of modular Poaceae-specific proteins. Mol Plant. 2016;9(4):514–27.

    Article  CAS  PubMed  Google Scholar 

  12. Karran P. DNA double strand break repair in mammalian cells. Curr Opin Genet Dev. 2000;10(2):144–50.

    Article  CAS  PubMed  Google Scholar 

  13. Haber JE. Partners and pathways repairing a double-strand break. Trends Genet. 2000;16(6):259–64.

    Article  CAS  PubMed  Google Scholar 

  14. Cassidy CL, Lemon JA, Boreham DR. Impacts of low-dose gamma-radiation on genotoxic risk in aquatic ecosystems. Dose Response. 2007;5(4):323–32.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Zhou BB, Elledge SJ. The DNA damage response: putting checkpoints in perspective. Nature. 2000;408(6811):433–9.

    Article  CAS  PubMed  Google Scholar 

  16. Paques F, Haber JE. Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. Microbiol Mol Biol Rev. 1999;63(2):349–404.

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Lavin MF, Kozlov S. ATM activation and DNA damage response. Cell Cycle. 2007;6(8):931–42.

    Article  CAS  PubMed  Google Scholar 

  18. Lopez-Contreras AJ, Fernandez-Capetillo O. The ATR barrier to replication-born DNA damage. DNA Repair (Amst). 2010;9(12):1249–55.

    Article  CAS  Google Scholar 

  19. Sacco E, Hasan MM, Alberghina L, Vanoni M. Comparative analysis of the molecular mechanisms controlling the initiation of chromosomal DNA replication in yeast and in mammalian cells. Biotechnol Adv. 2012;30(1):73–98.

    Article  CAS  PubMed  Google Scholar 

  20. Mazouzi A, Velimezi G, Loizou JI. DNA replication stress: causes, resolution and disease. Exp Cell Res. 2014;329(1):85–93.

    Article  CAS  PubMed  Google Scholar 

  21. Errico A, Costanzo V. Mechanisms of replication fork protection: a safeguard for genome stability. Crit Rev Biochem Mol Biol. 2012;47(3):222–35.

    Article  CAS  PubMed  Google Scholar 

  22. Jin YW, Na YJ, Lee YJ, An S, Lee JE, Jung M, Kim H, Nam SY, Kim CS, Yang KH, Kim SU, Kim WK, Park WY, Yoo KY, Kim CS, Kim JH. Comprehensive analysis of time- and dose-dependent patterns of gene expression in a human mesenchymal stem cell line exposed to low-dose ionizing radiation. Oncol Rep. 2008;19(1):135–44.

    CAS  PubMed  Google Scholar 

  23. Koo KM, Jung S, Kim J-B, Kim SH, Kwon SJ, Jeong W-J, Chung GH, Kang SY, Choi YE, Ahn JW. Effect of ionizing radiation on the DNA damage response in Chlamydomonas reinhardtii. Genes Genomics. 2017;39:63–75.

    Article  CAS  Google Scholar 

  24. Alscher RG, Donahue JL, Cramer CL. Reactive oxygen species and antioxidants: relationships in green cells. Physiol Plant. 1997;100:224–36.

    Article  CAS  Google Scholar 

  25. Saha P, Mukherjee A, Biswas AK. Modulation of NaCl induced DNA damage and oxidative stress in mungbean by pretreatment with sublethal dose. Biol Plant. 2015;59(1):139-146.

    Article  CAS  Google Scholar 

  26. Lopez E, Arce C, Oset-Gasque MJ, Canadas S, Gonzalez MP. Cadmium induces reactive oxygen species generation and lipid peroxidation in cortical neurons in culture. Free Radic Biol Med. 2006;40(6):940–51.

    Article  CAS  PubMed  Google Scholar 

  27. Xiang Y, Song M, Wei Z, Tong J, Zhang L, Xiao L, Ma Z, Wang Y. A jacalin-related lectin-like gene in wheat is a component of the plant defence system. J Exp Bot. 2011;62(15):5471–83.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Gorlach J, Volrath S, Knauf-Beiter G, Hengy G, Beckhove U, Kogel KH, Oostendorp M, Staub T, Ward E, Kessmann H, Ryals J. Benzothiadiazole, a novel class of inducers of systemic acquired resistance, activates gene expression and disease resistance in wheat. Plant Cell. 1996;8(4):629–43.

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Patra J, Sahoo MK, Panda BB. Salicylic acid triggers genotoxic adaptation to methyl mercuric chloride and ethyl methane sulfonate, but not to maleic hydrazide in root meristem cells of Allium cepa L. Mutat Res. 2005;581(1–2):173–80.

    Article  CAS  PubMed  Google Scholar 

  30. Gichner T, Menke M, Stavreva DA, Schubert I. Maleic hydrazide induces genotoxic effects but no DNA damage detectable by the comet assay in tobacco and field beans. Mutagenesis. 2000;15(5):385–9.

    Article  CAS  PubMed  Google Scholar 

  31. Dona M, Macovei A, Fae M, Carbonera D, Balestrazzi A. Plant hormone signaling and modulation of DNA repair under stressful conditions. Plant Cell Rep. 2013;32(7):1043–52.

    Article  CAS  PubMed  Google Scholar 

  32. Mur LA, Kenton P, Atzorn R, Miersch O, Wasternack C. The outcomes of concentration-specific interactions between salicylate and jasmonate signaling include synergy, antagonism, and oxidative stress leading to cell death. Plant Physiol. 2006;140(1):249–62.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Mhamdi A, Hager J, Chaouch S, Queval G, Han Y, Taconnat L, Saindrenan P, Gouia H, Issakidis-Bourguet E, Renou JP, Noctor G. Arabidopsis GLUTATHIONE REDUCTASE1 plays a crucial role in leaf responses to intracellular hydrogen peroxide and in ensuring appropriate gene expression through both salicylic acid and jasmonic acid signaling pathways. Plant Physiol. 2010;153(3):1144–60.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Han Y, Chaouch S, Mhamdi A, Queval G, Zechmann B, Noctor G. Functional analysis of Arabidopsis mutants points to novel roles for glutathione in coupling H (2) O (2) to activation of salicylic acid accumulation and signaling. Antioxid Redox Signal. 2013;18(16):2106–21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Han Y, Mhamdi A, Chaouch S, Noctor G. Regulation of basal and oxidative stress-triggered jasmonic acid-related gene expression by glutathione. Plant Cell Environ. 2013;36(6):1135–46.

    Article  CAS  PubMed  Google Scholar 

  36. Hwang IS, Hwang BK. The pepper mannose-binding lectin gene CaMBL1 is required to regulate cell death and defense responses to microbial pathogens. Plant Physiol. 2011;155(1):447–63.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Hadwiger LA, Tanaka K. Non-host resistance: DNA damage is associated with SA signaling for induction of PR genes and contributes to the growth suppression of a pea pathogen on pea endocarp tissue. Front Plant Sci. 2017;8:446.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Ciccia A, Elledge SJ. The DNA damage response: making it safe to play with knives. Mol Cell. 2010;40(2):179–204.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Springer PS, McCombie WR, Sundaresan V, Martienssen RA. Gene trap tagging of PROLIFERA, an essential MCM2-3-5-like gene in Arabidopsis. Science. 1995;268(5212):877–80.

    Article  CAS  PubMed  Google Scholar 

  40. Bell SP. The origin recognition complex: from simple origins to complex functions. Genes Dev. 2002;16(6):659–72.

    Article  CAS  PubMed  Google Scholar 

  41. Coleman TR, Carpenter PB, Dunphy WG. The Xenopus Cdc6 protein is essential for the initiation of a single round of DNA replication in cell-free extracts. Cell. 1996;87(1):53–63.

    Article  CAS  PubMed  Google Scholar 

  42. Nishitani H, Lygerou Z, Nishimoto T, Nurse P. The Cdt1 protein is required to license DNA for replication in fission yeast. Nature. 2000;404(6778):625–8.

    Article  CAS  PubMed  Google Scholar 

  43. Cho JH, Kim HB, Kim HS, Choi SB. Identification and characterization of a rice MCM2 homologue required for DNA replication. BMB Rep. 2008;41(8):581–6.

    Article  CAS  PubMed  Google Scholar 

  44. Dang HQ, Tran NQ, Gill SS, Tuteja R, Tuteja N. A single subunit MCM6 from pea promotes salinity stress tolerance without affecting yield. Plant Mol Biol. 2011;76(1–2):19–34.

    Article  CAS  PubMed  Google Scholar 

  45. Aklilu BB, Soderquist RS, Culligan KM. Genetic analysis of the replication protein a large subunit family in Arabidopsis reveals unique and overlapping roles in DNA repair, meiosis and DNA replication. Nucleic Acids Res. 2014;42(5):3104–18.

    Article  CAS  PubMed  Google Scholar 

  46. Pursell ZF, Kunkel TA. DNA polymerase epsilon: a polymerase of unusual size (and complexity). Prog Nucleic Acid Res Mol Biol. 2008;82:101–45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Johnson RE, Klassen R, Prakash L, Prakash S. A major role of DNA polymerase delta in replication of both the leading and lagging DNA strands. Mol Cell. 2015;59(2):163–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Pedroza-Garcia JA, Mazubert C, Del Olmo I, Bourge M, Domenichini S, Bounon R, Tariq Z, Delannoy E, Pineiro M, Jarillo JA, Bergounioux C, Benhamed M, Raynaud C. Function of the plant DNA polymerase epsilon in replicative stress sensing, a genetic analysis. Plant Physiol. 2017;173(3):1735–49.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Pedroza-Garcia JA, Domenichini S, Mazubert C, Bourge M, White C, Hudik E, Bounon R, Tariq Z, Delannoy E, Del Olmo I, Pineiro M, Jarillo JA, Bergounioux C, Benhamed M, Raynaud C. Role of the polymerase ϵ sub-unit DPB2 in DNA replication, cell cycle regulation and DNA damage response in Arabidopsis. Nucleic Acids Res. 2016;44(15):7251–66.

    CAS  PubMed  PubMed Central  Google Scholar 

  50. Culligan K, Tissier A, Britt A. ATR regulates a G2-phase cell-cycle checkpoint in Arabidopsis thaliana. Plant Cell. 2004;16(5):1091–104.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Culligan KM, Robertson CE, Foreman J, Doerner P, Britt AB. ATR and ATM play both distinct and additive roles in response to ionizing radiation. Plant J. 2006;48(6):947–61.

    Article  CAS  PubMed  Google Scholar 

  52. Abraham RT. Cell cycle checkpoint signaling through the ATM and ATR kinases. Genes Dev. 2001;15(17):2177–96.

    Article  CAS  PubMed  Google Scholar 

  53. Canman CE, Lim DS, Cimprich KA, Taya Y, Tamai K, Sakaguchi K, Appella E, Kastan MB, Siliciano JD. Activation of the ATM kinase by ionizing radiation and phosphorylation of p53. Science. 1998;281(5383):1677–9.

    Article  CAS  PubMed  Google Scholar 

  54. Czornak K, Chughtai S, Chrzanowska KH. Mystery of DNA repair: the role of the MRN complex and ATM kinase in DNA damage repair. J Appl Genet. 2008;49(4):383–96.

    Article  PubMed  Google Scholar 

  55. Harper JW, Elledge SJ. The DNA damage response: ten years after. Mol Cell. 2007;28(5):739–45.

    Article  CAS  PubMed  Google Scholar 

  56. Williams RS, Williams JS, Tainer JA. Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template. Biochem Cell Biol. 2007;85(4):509–20.

    Article  CAS  PubMed  Google Scholar 

  57. Cimprich KA, Cortez D. ATR: an essential regulator of genome integrity. Nat Rev Mol Cell Biol. 2008;9(8):616–27.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Robison JG, Elliott J, Dixon K, Oakley GG. Replication protein a and the Mre11.Rad50.Nbs1 complex co-localize and interact at sites of stalled replication forks. J Biol Chem. 2004;279(33):34802–10.

    Article  CAS  PubMed  Google Scholar 

  59. Koga A, Ishibashi T, Kimura S, Uchiyama Y, Sakaguchi K. Characterization of T-DNA insertion mutants and RNAi silenced plants of Arabidopsis thaliana UV-damaged DNA binding protein 2 (AtUV-DDB2). Plant Mol Biol. 2006;61(1–2):227–40.

    Article  CAS  PubMed  Google Scholar 

  60. Molinier J, Lechner E, Dumbliauskas E, Genschik P. Regulation and role of Arabidopsis CUL4-DDB1A-DDB2 in maintaining genome integrity upon UV stress. PLoS Genet. 2008;4(6):e1000093.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  61. Miller JH. Mutators in Escherichia coli. Mutat Res. 1998;409(3):99–106.

    Article  CAS  PubMed  Google Scholar 

  62. Fishel R. Mismatch repair. J Biol Chem. 2015;290(44):26395–403.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Franchitto A, Pichierri P, Piergentili R, Crescenzi M, Bignami M, Palitti F. The mammalian mismatch repair protein MSH2 is required for correct MRE11 and RAD51 relocalization and for efficient cell cycle arrest induced by ionizing radiation in G2 phase. Oncogene. 2003;22(14):2110–20.

    Article  CAS  PubMed  Google Scholar 

  64. Clough SJ, Bent AF. Floral dip: a simplified method for agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 1998;16(6):735–43.

    Article  CAS  PubMed  Google Scholar 

  65. Koo KM, Jung S, Lee BS, Kim JB, Jo YD, Choi HI, Kang SY, Chung GH, Jeong WJ, Ahn JW. The mechanism of starch over-accumulation in Chlamydomonas reinhardtii high-starch mutants identified by comparative Transcriptome analysis. Front Microbiol. 2017;8:858.

    Article  PubMed  PubMed Central  Google Scholar 

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This work was funded by the research program of Korea Atomic Energy Research Institute, Republic of Korea. This funding body did not play any role in the design of this study and collection, analysis, and interpretation of data and in writing the manuscript.

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IJJ generated transgenic lines and analyzed data for transgenic plants. JWA performed transcriptome analysis, wrote the manuscript and arranged all data. IJJ and SJ carried out RT-PCR analysis. JEH and MJH helped to design experiments. HIC helped to analyze transcriptome data. JBK supervised the work and interpreted data. All authors contributed revision of the manuscript. All authors read and approved the manuscript.

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Correspondence to Jin-Baek Kim.

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Supplementary information

Additional file 1: Figure S1.

Root growth of OsJAC1-overexpressing plants in response to salt stress.

Additional file 2: Table S1.

Expression levels of anotated transciprts in OsJAC1-overexpressing Arabidopsis lines.

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Jung, I.J., Ahn, JW., Jung, S. et al. Overexpression of rice jacalin-related mannose-binding lectin (OsJAC1) enhances resistance to ionizing radiation in Arabidopsis. BMC Plant Biol 19, 561 (2019).

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