Next Article in Journal
Kinase Activity of PAR1b, Which Mediates Nuclear Translocation of the BRCA1 Tumor Suppressor, Is Potentiated by Nucleic Acid-Mediated PAR1b Multimerization
Previous Article in Journal
In Vitro Selection and Characterization of HIV-1 Variants with Increased Resistance to LP-40, Enfuvirtide-Based Lipopeptide Inhibitor
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 23
Issue 12
10.3390/ijms23126622
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

OsASR6 Alleviates Rice Resistance to Xanthomonas oryzae via Transcriptional Suppression of OsCIPK15

by
Weiyi Guo
1,
Songyu Chen
1,
Youping Xu
2 and
Xinzhong Cai
1,3,*
1
Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, College of Agriculture and Biotechnology, Zhejiang University, 866 Yu Hang Tang Road, Hangzhou 310058, China
2
Centre of Analysis and Measurement, Zhejiang University, 866 Yu Hang Tang Road, Hangzhou 310058, China
3
Hainan Institute, Zhejiang University, Sanya 572025, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(12), 6622; https://doi.org/10.3390/ijms23126622
Submission received: 13 May 2022 / Revised: 11 June 2022 / Accepted: 13 June 2022 / Published: 14 June 2022
(This article belongs to the Section Molecular Plant Sciences)
Browse Figures
Versions Notes

Abstract

:
The plant-specific ASR (abscisic acid, stress and ripening) transcription factors are pivotal regulators of plant responses to abiotic stresses. However, their functions in plant disease resistance remain largely unknown. In this study, we revealed the role of OsASR6 in rice plants’ resistance to two important bacterial diseases caused by Xanthomonas oryzae pv. oryzae (Xoo) and X. oryzae pv. oryzicola (Xoc) and elucidated the mechanisms underlying OsASR6-regulated resistance. The expression of OsASR6 was strongly elevated in response to both Xoo and Xoc challenges. Silencing of OsASR6 in OsASR6-RNAi transgenic plants markedly enhanced rice resistance to the two bacterial pathogens. Moreover, comparative transcriptome analyses for OsASR6-RNAi and wild-type plants inoculated and uninoculated with Xoc demonstrated that OsASR6 suppressed rice resistance to Xoc by comprehensively fine-tuning CIPK15- and WRKY45-1-mediated immunity, SA signaling and redox homeostasis. Further luciferase reporter assays confirmed that OsASR6 negatively regulated CIPK15 but not WRKY45-1 expression in planta. Overexpression of OsCIPK15 strongly enhanced rice resistance to Xoo and Xoc. Collectively, these results reveal that OsASR6 alleviates rice resistance through the transcriptional suppression of OsCIPK15, and thus links calcium signaling to rice resistance against X. oryzae. Our findings provide insight into the mechanisms underlying OsASR6-mediated regulation of rice resistance to X. oryzae.

1. Introduction

Bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo) and bacterial leaf streak caused by X. oryzae pv. oryzicola (Xoc) are devastating and economically important rice diseases [1]. Rice resistance to Xoo is conferred by resistance (R) genes. Up to now, 44 R genes conferring resistance to diverse strains of Xoo have been identified, of which 15 have been successfully cloned and characterized [2]. Unlike the resistance to Xoo, the rice resistance to Xoc seems not to comply with the gene-for-gene theory and thus is not controlled by the qualitative R gene. On the contrary, it is conferred by multiple quantitative trait loci (QTL) such as qBlsr5a and Xo1 [3,4]. In addition, rice WRKY45-1, OsMPK6, OsImpα1a and OsImpα1b influence resistance to Xoo and Xoc [5,6,7]. The identification of novel modulators should provide more insight into the resistance of rice to these pathogens and put forward new strategies to control these rice bacterial diseases.
The abscisic acid, stress and ripening (ASR) proteins are highly hydrophilic plant-specific low-molecular-weight proteins that usually function as transcription factors (TFs) [8]. They are well-known regulators of plant responses to abiotic stresses such as drought, cold and Al tolerance [9,10,11,12]. For example, the overexpression of OsASR1 enhances cold tolerance in transgenic rice plants [9]; OsASR3 stands out as the best potential candidate for drought tolerance [10]; OsASR5 mediates aluminum tolerance through STAR1 and other aluminum-responsive genes and promotes drought tolerance via a stomatal closure pathway associated with ABA and H2O2 signaling in rice [11,12]. In contrast to the well-known roles of ASRs in abiotic stress response, their functions in plants’ resistance to biotic stimuli are still not well understood. In rice, to date, only one report for OsASR2 is publicly available. OsASR2 positively regulates the resistance to Xoo and Rhizoctonia solani through promoting expression of the defense-related gene Os2H16 via targeting the GT-1 cis-element [13]. Notably, ASR exists as a small family in plants and family members may function differentially [8,10]. For example, the binding site of different OsASRs in promoters of their target genes may be distinct, GT-1 cis-element (GAAAAA) for OsASR2 while GGCCCAT and AGCCCAT cis-elements for OsASR5 [11,13]. Therefore, the functions of ASR members other than OsASR2 in rice defense against Xoo and Xoc remain to be dissected.
This study aimed to reveal the role of OsASR6 in rice resistance to the two important bacterial pathogens Xoo and Xoc and to elucidate the mechanisms underlying this resistance. We discovered that, unlike OsASR2, which promotes rice resistance to Xoo, OsASR6 suppresses rice resistance to Xoo and Xoc. Furthermore, we demonstrated that OsASR6 alleviates rice resistance via transcriptional repression of OsCIPK15, the positive resistance modulator.

2. Results

2.1. OsASR6 Strongly Responds to Xoc and Xoo Challenges in Rice

To analyze the possible involvement of OsASR6 in rice defense, we examined its expression in response to bacterial pathogens Xoc strain oxy04 and Xoo strain PXO99 in wild-type (WT) rice cultivar Nipponbare, which carries no known R gene conferring resistance to the above strains and thus is susceptible to them [14]. OsASR6 expression in oxy04-inoculated rice leaves was significantly induced by 19.2 folds, compared with that in the sterilized H2O mock-infiltrated leaves at 5 d post inoculation (dpi) when the Xoc-infiltrated areas just began to show water-soaked symptoms. Likely, after clipping inoculation with PXO99, OsASR6 expression was markedly enhanced by 16.5 folds in comparison with that in the mock-clipped control at 5 dpi when the clipping-inoculated edges initiated the necrotic symptom (Figure 1). The high sensitivity of OsASR6 in expression to pathogen inoculations indicated that OsASR6 is very likely involved in rice resistance to these pathogens.

2.2. Silencing of OsASR6 Enhances Rice Resistance to Xoc

To assess the function of OsASR6 in rice disease resistance, we constructed rice transgenic lines in which OsASR6 was silenced (OsASR6-RNAi) using pANDA vector based on pUC12 with the hygromycin B resistance gene (Figure 2A). Both hygromycin resistance detection and PCR amplification for the hygromycin B gene confirmed that this gene had been integrated into the genome of the transgenic rice plants (Figure S1). Moreover, the OsASR6 gene expression was analyzed in 5-week-old T2 plants using quantitative real-time PCR (qRT-PCR). As shown in Figure 2B, OsASR6 expression was significantly suppressed in OsASR6-RNAi lines compared with that in WT plants. These results demonstrated that these OsASR6-RNAi lines are real transgenic rice plants with a suppressed expression level of the OsASR6 gene.
To further evaluate the role of OsASR6 in rice resistance to the important bacterial pathogen Xoc, we analyzed the effect of modulation of OsASR6 gene expression on plant disease resistance. We comparatively examined the resistance of WT and the T2 generation of OsASR6-RNAi transgenic plants to Xoc strain oxy04. To obtain more accurate results, we merely conducted statistical analyses for inoculation results collected from leaves from the same positions on plants. The inoculation analyses showed that the leaves of the inoculated OsASR6-RNAi plants only generated characteristic water-soaked lesions with restricted extension, while those of the inoculated WT plants formed much larger lesions with significant extension along the veins and produced plenty of yellow bacterial oozes on the lesions (Figure 2C). The average lesion length of OsASR6-RNAi leaves of lines 1, 2 and 3 reached 1.13, 0.97 and 1.05 cm, respectively at 10 dpi, compared with 2.42 cm in leaves of WT plants (Figure 2D). Further in planta bacterial-colony counting analysis showed that inoculated leaves of OsASR6-RNAi plants only accumulated about 1.7, 1.2 and 1.2% of the bacterial amount of inoculated WT leaves at 10 dpi (Figure 2E). Taken together, these results demonstrated that OsASR6 strongly negatively tunes rice resistance to Xoc.

2.3. Silencing of OsASR6 Promotes Rice Resistance to Xoo

To further probe the role of OsASR6 in rice resistance to another important bacterial pathogen Xoo, we examined the resistance of WT and the OsASR6-RNAi transgenic plants to Xoo strain PXO99. At 14 dpi, all three OsASR6-RNAi lines were more resistant to PXO99, with lesion lengths of 7.5, 7.5 and 8.7 cm, respectively, compared with 15.3 cm for WT plants (Figure 3A,B). Further in planta bacterial-colony counting analysis showed that inoculated leaves of OsASR6-RNAi plants only accumulated about 7.7, 8.3 and 9.8% of bacterial level of inoculated WT leaves at 14 dpi (Figure 3C). These results demonstrated that the OsASR6-RNAi lines were more resistant to PXO99 and thus OsASR6 negatively modulates rice resistance to Xoo.

2.4. Global Transcriptome Analysis Identifies the Genes Likely Involved in Rice Resistance to Xoc

ASRs usually function as transcription factors (TFs) [8,15]. Amino acid sequence alignment of OsASR6 with SlASR1 and OsASR2 showed that OsASR6 contained the conserved ABA_WDS domain at residues 89–161 and the potential DNA-binding region at residues 124–181 (Figure 4A), which corresponds to the DNA-binding domain experimentally verified in SlASR1 [15]. Therefore, to understand the mechanisms underlying OsASR6-dependent modulation of rice resistance, we performed transcriptome analysis employing the OsASR6-RNAi plants. Leaves from 8-week-old WT and OsASR6-RNAi rice plants either inoculated with Xoc strain oxy04 or mock treated with sterilized H2O were harvested at 5 dpi to generate four RNA libraries for transcriptome analysis: the sterilized H2O mock-inoculated WT samples, the oxy04 inoculated WT samples, the sterilized H2O mock-inoculated OsASR6-RNAi samples and the oxy04 inoculated OsASR6-RNAi samples. The raw data from these transcriptome analyses were deposited in NCBI (PRJNA842942) and provided in the Supplemental Table S1.
The criteria for significantly differentially expressed genes (DEGs), including significantly upregulated genes (URGs) and significantly downregulated genes (DRGs), were set as fold change >2 (for URGs) or <−2 (for DRGs) and p value < 0.05 in three biological replicates. Based on these criteria, a total of 3378 DEGs including 2640 URGs and 738 DRGs were identified to be responsive to Xoc invasion in the WT rice plants based on the comparison between WT-Xoc and WT-mock (Table S2 and Figure 4B), while 1952 DEGs including 1201 URGs and 751 DRGs were responsive to Xoc infection in the OsASR6-RNAi plants based on the comparison between OsASR6-RNAi-Xoc and OsASR6-RNAi-mock (Table S3 and Figure 4B). Additionally, 3780 DEGs including 2208 URGs and 1572 DRGs were affected by OsASR6 silencing based on the comparison between OsASR6-RNAi and WT (Table S4 and Figure 4B).
Genes potentially involved in OsASR6 function in suppressing constitutive and Xoc-responsive rice resistance were identified from DEGs. The DEGs generated from the comparison between groups OsASR6-RNAi and WT represent the candidate targets of OsASR6 for constitutive resistance, while the DEGs exhibiting opposite abundance alteration in response to Xoc inoculation in WT plants (comparison WT-Xoc/WT-mock) and in OsASR6-RNAi plants (comparison OsASR6-RNAi-Xoc/OsASR6-RNAi-mock) or those differentiated merely in one of the above two comparisons represent the candidate targets of OsASR6 for Xoc-responsive resistance, considering that OsASR6 strongly repressed rice resistance to Xoc (Figure 4C). A total of 742 genes were DEGs of both comparisons. Among them, 252 showed the opposite trend of Xoc-responsive expression in the WT and OsASR6-RNAi plants (Table S5 and Figure 4C). These 252 DEGs represented the import source to identify the targets of OsASR6 in Xoc-responsive rice resistance.
Consequently, some targets of OsASR6 in Xoc-responsive rice resistance were identified from the 252 DEGs. Intriguing ones included a member of the nucleotide binding site (NBS) and leucine-rich repeat (LRR) class of plant disease resistance (R) gene PibH8 (Pyricularia oryzae resistance b H8), a positive resistance modulator asparagine synthetase gene ASN1 and a negative resistance modulator protein kinase gene CIPK5 (Calcineurin B-like protein-interacting protein kinase 5). PibH8 and ASN1 were significantly upregulated by Xoc inoculation in OsASR6-RNAi rice plants while strongly downregulated by Xoc inoculation in WT rice plants, whereas CIPK5 exhibited the opposite expression (Table 1, Tables S2 and S3). All the above genes are involved in plant disease resistance (refer to the Discussion section) and the expression–function match results of these genes coincide well with the negative role of OsASR6 in rice resistance to Xoc, demonstrating that these three genes are likely Xoc-responsive targets of OsASR6 in suppressing rice resistance. Other candidates included CDPK13, Annexin D4, SARD1, Cysteine-rich receptor-like protein kinase 4 and a set of genes involved in hormone signaling and redox homeostasis (Table 1).
In addition, targets of OsASR6 in Xoc-responsive rice resistance were also identified from the DEGs that were differentially expressed merely in one of the two comparisons (OsASR6-RNAi-Xoc/OsASR6-RNAi-mock and WT-Xoc/WT-mock) were also possible Xoc-responsive modulators of OsASR6-suppressive rice resistance. Some of these interesting DEGs included PAMP-induced defense regulation gene CIPK15, anti-Xoc defense negative modulator gene WRKY45-1, anti-Xoo defense negative modulator gene WRKY76, key gene of ethylene biosynthesis ACS2 (ACC synthase 2), salicylic acid (SA) carboxymethyl transferase gene (SAMT), and other defense-related genes Hsp90, PR1a, CIPK11, CIPK14 and MAPKK5 (Table 1, Tables S2 and S3). Other candidates of this type are listed in Table 1.
Moreover, silencing of OsASR6 caused 3780 genes to significantly alter their transcript abundance. Among these DEGs, which were differentially expressed in between the OsASR6-RNAi plants and the WT plants, the plant immunity activator that promotes SA production SARD1 and jasmonic acid (JA) inducible rice PR10 JIOsPR10 were significantly upregulated in the OsASR6-RNAi plants, while two key genes of gibberellic acid (GA) pathway Gibberellin 20 oxidase 1 and Gibberellin 20 oxidase 2 were remarkably downregulated in the OsASR6-RNAi plants than in the WT plants (Table 2 and Table S4). Therefore, SARD1, JIOsPR10, Gibberellin 20 oxidase 1 and Gibberellin 20 oxidase 2 seemed to be promising candidates of constitutive modulators of OsASR6-suppressive rice resistance, and OsASR6 might repress rice resistance via the tuning of the SARD1-mediated SA production, JIOsPR10-mediated JA pathway and Gibberellin 20 oxidase 1- and Gibberellin 20 oxidase 2-mediated GA signaling. Other candidates of this type included PibH8, ASN1, CDPKs, WRKYs, CIPKs and a set of redox homeostasis genes (Table 2).
Interestingly, some genes such as PibH8, ASN1, WRKYs and CIPKs were potential targets of OsASR6 function in suppressing both constitutive and Xoc-responsive rice resistance (Table 1 and Table 2).

2.5. Quantitative Real-Time PCR Validation of Genes Probably Involved in OsASR6-Suppressive Rice Resistance to Xoc

To confirm the transcriptome analysis results, quantitative real-time PCR (qRT-PCR) experiments were performed to validate the expression patterns of 10 DEGs likely involved in OsASR6-suppressive rice resistance to Xoc, including CIPK15, WRKY45-1, ACS2, WRKY76, JAMT1, PibH8, ASN1, CIPK5, Hsp90 and SAMT. The results showed that the expression patterns of these 10 genes obtained from qRT-PCR analysis were generally consistent with those from the transcriptome analysis in both OsASR6-RNAi-Xoc/OsASR6-RNAi-mock and WT-Xoc/WT-mock comparisons (Figure 5). These analyses demonstrated that the results of the transcriptome analysis are reliable, and that these genes are potential targets of OsASR6 function in suppressing rice resistance.

2.6. OsASR6 Suppresses CIPK15 Expression in Planta

The ASR proteins usually act as transcription factors [8]. In order to further confirm whether OsASR6 can regulate the expression of its potential target genes revealed by the transcriptome analysis in planta, we carried out transient luciferase reporter gene expression detection assays in Nicotiana benthamiana for three selected genes including CIPK15, WRKY45-1 and RAP2-13. CIPK15 was chosen since CIPKs represent important components of calcium early signaling whose function in rice resistance to X. oryzae remains unclear and it is the only DEG of CIPK type whose role in rice immunity was reported [16]. Rice WRKY45-1 influences resistance to Xoo and Xoc [5] while RAP2-13 is involved in ethylene signaling, which modulates rice resistance [17]. The 2.0 kb promoter of CIPK15 normally drove the expression of the luciferase gene (CIPK15 p:LUC) when the GFP tag was co-expressed (Figure 6A left half of leaf). However, co-expression of GFP-OsASR6 strongly suppressed the luciferase gene expression driven by the CIPK15 promoter (Figure 6A right half of leaf). Quantitative analysis showed that the signal of CIPK15 p:LUC co-expressed with GFP-OsASR6 was only 32% of that of co-expression of CIPK15 p:LUC and GFP (Figure 6A). These results indicated that OsASR6 suppresses CIPK15 gene expression in planta.
The same assay was also conducted for WRKY45-1 and RAP2-13, the other two putative target genes of OsASR6 revealed by the transcriptome analysis. Results showed that the 2.0 kb promoter of WRKY45-1 and RAP2-13 normally drove expression of luciferase gene (WRKY45-1 p:LUC) and (RAP2-13 p:LUC), respectively, when the GFP tag was co-expressed (Figure 6B left half of leaf). Co-expression of GFP-OsASR6 did not alter significantly the luciferase gene expression driven by WRKY45-1 and RAP2-13 promoter, respectively (Figure 6B right half of leaf). Quantitative analysis showed that the signal of WRKY45-1 p:LUC or RAP2-13 p:LUC co-expressed with GFP-OsASR6 was 106% and 108% of that of their co-expression with GFP (Figure 6B). These analyses demonstrated that OsASR6 does not directly regulate WRKY45-1 and RAP2-13 gene expression in planta.

2.7. Overexpression of OsCIPK15 Enhances Rice Resistance to Xoc

The result that OsASR6 negatively regulates OsCIPK15 expression in planta prompted us to probe the function of OsCIPK15 in rice resistance. We constructed three OsCIPK15-overexpression (OsCIPK15-OE) rice transgenic lines driven by promoter of a maize ubiquitin gene using pCZD vector with the hygromycin B resistance gene (Figure 7A). Both hygromycin resistance detection and PCR amplification for the hygromycin B gene confirmed that this gene had been integrated into the genome of the transgenic rice plants (Figure S2). Moreover, expression of OsCIPK15 was analyzed in 5-week-old T2 plants using qRT-PCR. As shown in Figure 7B, OsCIPK15 expression was significantly increased by over 8-fold in OsCIPK15-OE lines compared with that in WT plants. These results demonstrated that these OsCIPK15-OE lines are real transgenic rice plants with enhanced expression level of the OsCIPK15 gene.
The confirmed T2 generation of OsCIPK15-OE transgenic plants were inoculated with Xoc strain oxy04 by bacterial infiltration. The inoculation analyses showed that the inoculated leaves of OsCIPK15-OE plants only generated characteristic water-soaked lesions with restricted extension, while the inoculated leaves of WT plants formed much larger lesions with significant extension along the veins and produced plenty of yellow bacterial oozes on the lesions (Figure 7C). The average lesion length of OsCIPK15-OE leaves of lines 1, 2 and 3 reached 1.20 cm, 1.19 cm and 1.05 cm, respectively at 10 dpi, compared with 2.23 cm in leaves of WT plants (Figure 7D). Further in planta bacterial colony counting analysis showed that inoculated leaves of OsCIPK15-OE plants only accumulated 1.7%, 1.5% and 1.2% of bacterial amount in those of WT leaves at 10 dpi (Figure 7E). Collectively, these results demonstrated that the OsCIPK15-OE lines were much more resistant to oxy04 than WT plants and thus OsCIPK15 plays a strong positive role in rice resistance to Xoc.

2.8. Overexpression of OsCIPK15 Increases Rice Resistance to Xoo

To further determine the role of OsCIPK15 in rice resistance to another important bacterial pathogen Xoo, we examined the resistance of the OsCIPK15-OE transgenic rice plants to Xoo strain PXO99. At 14 dpi, all three OsCIPK15-OE lines were more resistant to PXO99, with lesion lengths of 7.3, 7.8 and 7.2 cm, respectively, compared with 13.3 cm for WT plants (Figure 8A,B). Further in planta bacterial-colony counting analysis showed that inoculated leaves of OsCIPK15-OE plants only accumulated 8.9, 12.8 and 6.9% of the bacterial amount in those of WT plants at 14 dpi (Figure 8C). These results indicated that the OsCIPK15-OE lines were more resistant to PXO99 than WT plants and thus OsCIPK15 positively modulates rice resistance to Xoo.
Together with our finding that OsASR6 negatively regulates OsCIPK15 expression in planta, these results reveal that OsASR6 alleviates rice resistance via transcriptional suppression of OsCIPK15, which encodes for a calcium sensor CBL-interacting protein, and thus links the calcium signaling to rice resistance against Xoc.

3. Discussion

ASR genes are plant-specific but broadly exist in the plant kingdom, ranging from ancient gymnosperms to angiosperms including both dicots and monocots [8]. Although their essential roles in ABA response and abiotic stress tolerance have been well known [8,9,10,11,12], the functions of ASRs in plant disease resistance remain poorly understood, which is manifested by the very limited availability of publications [8,13,18]. In this study, we provided genetic evidence to demonstrate that OsASR6 functions as a suppressor of rice resistance to both Xoc and Xoo and thus exhibits a high potential in rice molecular breeding for improved disease resistance. Previous documents have recorded the function of OsASR2 in rice resistance against Rhizoctonia solani and Xoo [13] and the roles of OsASR1, OsASR3 and OsASR5 in rice tolerance to cold, drought and aluminum [9,10,11,12]. Together, these results strongly indicate that the OsASR family plays broad and crucial roles in regulating rice responses to both biotic and abiotic stresses and thus represents excellent gene resources for rice molecular breeding for improved yields.
Notably, OsASR6 alleviates rice resistance through transcriptional suppression of OsCIPK15, while OsASR2 promotes rice resistance through enhancing expression of Os2H16 [13]. Thus OsASR6 and OsASR2 play opposite roles with distinct mechanisms in rice disease resistance. The remaining question is how these OsASRs coordinate in regulating rice disease resistance.
The mechanisms that underlie OsASR-regulated rice disease resistance remain largely unknown. The only report available to date is that OsASR2 positively regulates the resistance to Xoo and Rhizoctonia solani through promoting the expression of the defense-related gene Os2H16 by targeting the GT-1 cis-element [13]. In this study, we provided evidence from transcriptome and LUC reporter expression analyses to uncover the role of OsCIPK15 in OsASR6-suppressive rice resistance to Xoo and Xoc. The contribution of CIPKs to plant resistance has previously been documented. For example, TaCIPK5 and TaCIPK10 are required for wheat resistance to stripe rust fungus Puccinia striiformis f.sp. tritici [19,20]. SlCIPK6 contributes to AvrPto-triggered immunity against Pst DC3000 [21]. Interestingly, OsCIPK15 plays a crucial role in the PAMPs chitin and xylanase-induced defense signaling, including hypersensitive cell death, phytoalexin biosynthesis, and pathogenesis-related gene expression in cultured rice cells [16]. Our finding that OsCIPK15 is targeted by OsASR6 in modulating rice resistance to Xoo and Xoc extends the range of CIPK in plant disease resistance. Intriguingly, CIPKs interact with the calcium sensors CBLs. Therefore, our results link the calcium signaling to rice resistance to Xoo and Xoc. In this context, it is interesting that a set of calcium-signaling components such as annexin D4, CDPK3, CDPK10, CIPK11 and CIPK14 were identified as potential candidates of the OsASR6 targets. The role of these genes in OsASR6-suppressive rice resistance awaits further study. In addition, the CBLs interacting with OsCIPK15 and the targets of OsCIPK15 in OsASR6-suppressive rice resistance need further identification.
Our results from transcriptome and LUC reporter expression analyses demonstrate that OsASR6 directly downregulated OsCIPK15 gene expression. Nevertheless, the binding element of OsASR6 in the promoter of OsCIPK15 remains unidentified. The binding site of two of the six OsASRs was reported to date. OsASR2 could bind to the GT-1 cis-element (GAAAAA) while OsASR5 to GGCCCAT and AGCCCAT cis-elements [11,13]. Interestingly, three GAAAAA elements exist in the 2 kb promoter of OsCIPK15 (Figure S3). We further conducted EMSA analyses to determine whether OsASR6 can indeed bind to the binding cis-elements of OsASR2 and OsASR5. The His-tagged OsASR6 was expressed in E. coli, affinity purified and was then used for EMSA analyses. The biotinylated 4× GGCCCAT, 4× AGCCCAT and 4× GAAAAA were used as probes, while the excessive unlabeled version of these sequences and mutated sequences were used as WT competitors and mutant competitors, respectively. One band appeared corresponding to binding of OsASR6 to labeled 4× AGCCCAT, which could be specifically completed by an unlabeled 4× AGCCCAT but not a mutant one. This type of band was also observed for 4× GAAAAA in weaker signal but not for 4× GGCCCAT probe (Figure S4). However, these bands were weak and not severely retarded (Figure S4). Therefore, whether OsASR6 binds to the AGCCCAT and GAAAAA cis-elements requires further verification, and comparative study on the binding specificity of the OsASR family deserves to be conducted.
OsASR6 is a transcriptional suppressor of OsCIPK15. However, the expression of OsCIPK15 decreases in the OsASR6-RNAi transgenic plants (Table 2). This should be the consequence of suppressive modulation of the OsCIPK15 expression from repressor(s) other than OsASR6 in the OsASR6-RNAi plants, which is opposite to and stronger than the direct effect from OsASR6 on OsCIPK15 expression. That is, the expression of OsCIPK15 is not only modulated by OsASR6 but also affected by other factors. As a matter of fact, it was reported that hexoses, such as glucose, mannose, galactose and fructose, repressed OsCIPK15 expression [22]. In this context, we analyzed the DEG-enriched KEGG pathways related to the hexose metabolism and found that at least 17 DEG encoding enzymes involved in the biosynthesis of hexoses including glucose, mannose and fructose through the starch and sucrose metabolism (pathway ID: ko00500) and fructose and mannose metabolism (pathway ID: ko00051) KEGG pathways were significantly upregulated in the OsASR6-RNAi plants compared with WT plants (Table S6), which is expected to lead to the accumulation of these hexoses in the OsASR6-RNAi plants. The high level of hexoses, functioning as repressors of OsCIPK15 expression [22], causes strong reduction of the OsCIPK15 expression in the OsASR6-RNAi plants. On the other hand, in normal conditions, the expression level of OsASR6 is not high. Thus, in the OsASR6-RNAi plants, RNAi of OsASR6 may only cause a moderate increase of the OsCIPK15 expression, an effect much weaker than the repressing effect from the highly accumulated hexoses. Therefore, the net effect of the direct effect (upregulation of OsCIPK15 expression) and the indirect effect (accumulation of hexoses and thus reduction of OsCIPK15 expression) from the OsASR6 silencing in the OsASR6-RNAi plants is the decrease of the OsCIPK15 expression. When inoculated with Xoc, however, the contribution of OsASR6 and hexoses to the OsCIPK15 expression is reversed. The OsASR6 expression is strongly induced by Xoc (Figure 1) and thus should be profoundly suppressed in Xoc-inoculated OsASR6-RNAi plants, which leads to the strong induction of the OsCIPK15 expression. In contrast, most of the mentioned 17 DEGs involved in hexose biosynthesis were reduced or not significantly changed in Xoc-inoculated OsASR6-RNAi plants compared with Xoc-inoculated WT plants (Table S6). Therefore, in the Xoc-inoculated OsASR6-RNAi plants, the OsCIPK15 expression is dominantly affected by the silencing of OsASR6 rather than hexoses and thus the Xoc-inoculated OsASR6-RNAi plants are expected to exhibit enhanced OsCIPK15 expression compared with the Xoc-inoculated WT plants.
ASRs usually function as transcription factors (TFs) [8]. Therefore, to understand the mechanisms underlying OsASR6-mediated suppression of rice resistance, comprehensive transcriptome analyses for OsASR6-RNAi and wild-type plants inoculated and uninoculated with Xoc were performed to identify the potential transcriptional regulation targets of OsASR6. Given that OsASR6 negatively regulates rice resistance, the DEGs exhibiting opposite abundance alteration or only existing in one comparison in response to Xoc inoculation in WT plants (comparison between WT-Xoc and WT) and in OsASR6-RNAi plants (comparison between OsASR6-RNAi-Xoc and OsASR6-RNAi) represent the highly promising candidate targets of OsASR6. Consequently, 252 DEG genes showing opposite expression trends in response to Xoc inoculation in the WT and OsASR6-RNAi plants were identified (Table S5 and Figure 4C). These 252 genes represented the import source to identify the Xoc-responsive modulators of OsASR6-suppressive rice resistance. A large body of them are functionally unknown genes. However, interestingly, some genes have been reported to be involved in plant disease resistance. Besides CIPK15, these genes include WRKY45-1, WRKY76, ACS2, PibH8, ASN1, CIPK5 and SAMT (Table 1).
Among the list of interesting genes, WRKY45-1 negatively modulates rice resistance to Xoc [5]; WRKY76 negatively regulates rice resistance to rice bacterial blight and rice blast [23]; ACS2 is the key gene of ethylene biosynthesis and positively modulates rice basal disease resistance [17]; PibH8 is a member of the NBS-LRR class of plant R genes that confers rice resistance to rice blast [24]; ASN1 synthesizes asparagine from glutamine, while glutamine negatively regulates rice resistance to rice blast [25]; CIPK5 negatively affects Arabidopsis resistance to Pseudomonas syringae DC3000 and Hyaloperonospora arabidopsidis [26]; SAMT negatively regulates salicylic acid (SA) thereby influencing resistance in Arabidopsis [27]. Therefore, screening out the targets of OsASR6 from the above genes remains a valuable task to be accomplished. To do so, the direct binding and gene expression regulation by OsASR6 and function in resistance to Xoo and Xoc need to be analyzed.

4. Materials and Methods

4.1. Plant Materials and Growth Conditions

The rice (Oryza sativa) Japonica transgenic plants used in this study were constructed in Nipponbare ecotype background by Wuhan BioRun Biosciences Co., Ltd. (Wuhan, China). Rice plants were grown in a growth room providing illumination of ~800 μmoles/m2/s with a 16 h light/8 h dark photoperiod at 26–28 °C. Nicotiana benthamiana were grown in a plant growth room providing illumination of ~300 μmoles/m2/s at 23–25 °C with a 16/8 h day/night photoperiod. Seeds were stored at seed storage chamber at 4 °C.

4.2. RNA Isolation and Quantitative Real-Time PCR Analysis

The whole rice leaves were collected from 8-week-old plants after treatments at the indicated time points and total RNA was isolated by Trizol reagent (TAKARA, Dalian, China) following the instructions provided by the manufacturer. After DNA removal using DNase I (Vazyme, Nanjing, China), the RNA samples were reverse transcribed into cDNA using HiScript Ⅱ QRT SuperMix (Vazyme, Nanjing, China). The obtained cDNAs were used for gene expression detection analysis with quantitative real-time PCR (qRT-PCR). qRT-PCR was carried out using ChamQ SYBR qPCR Master Mix (Vazyme, Nanjing, China) according to the manufacturer’s instructions on a StepOne Real-Time PCR System (Applied Biosystems, Waltham, MA, USA). The following PCR program was used: 95 °C for 30 s, 95 °C for 5 s, and 60 °C for 45 s for 40 cycles, followed by a melting-curve program. Expression of a gene-of-interest was normalized by that of rice TFIIAγ5 gene (AK065182), which is not transcriptionally affected by the pathogen inoculation [28]. Relative gene expression values were calculated using the 2−ΔΔCt method [29]. Sequences of primers used for qRT-PCR analysis are listed in Supplemental Table S7. Experiments were repeated three times. Data were statistically analyzed using SPSS software. Significance of the differences between the mean values of three independent experiments was determined with Student’s t test (p < 0.05).

4.3. Pathogen Inoculation and Plant Resistance Analyses

Inoculum of the bacterial pathogen Xanthomonas oryzae pv. oryzae (Xoo) PXO99 was prepared as described [30]. Briefly, PXO99 was grown at 28 °C in nutrient agar (NA) containing the following reagents in g/L: sucrose, 10; polypeptone, 5; yeast extract, 1; beef extract, 3; and Bacto agar, 15; pH 7.0–7.2. Single colonies were transferred to liquid NA medium with agitation until its OD600 approached 0.5. The bacterial cells were collected and resuspended in ddH2O with an OD600 of 1.0. Eight-week-old rice plants with fully expanded leaves were inoculated using the leaf clipping method [31]. For X. oryzae pv. oryzicola (Xoc) oxy04, after single colony propagation culture in NA medium, the bacterial cells were collected and resuspended in ddH2O. The bacterial suspension was then infiltrated into fully expanded 8-week-old rice leaves with a sterilized needleless syringe. Xoo and Xoc inoculum with an OD600 of 1.0 was used for inoculation and symptoms were scored by measuring lesion length. After inoculation, plants were maintained in plant growth room with a 16/8 h light/dark photoperiod at 28–30 °C. Bacterial number counting in inoculated leaves was determined as reported [32].
The inoculation analysis was performed three times, each in at least 6 plants for each treatment and gene backgrounds. Data of the lesion length and bacterial number were statistically analyzed using SPSS software. Significance of the differences between the mean values of three independent experiments was determined with Student’s t test (p < 0.05).

4.4. Transcriptome Sequencing

Leaf samples from 8-week-old WT and OsASR6-RNAi rice plants (ssp. Japonica cv. Nipponbare) with or without Xoc strain oxy04 inoculation at 5 dpi were collected and immediately frozen in liquid nitrogen. Total RNA was extracted using Trizol reagent (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s procedure, and checked for quantity and purity by Bioanalyzer 2100 and RNA 6000 Nano LabChip Kit (Agilent, Santa Clara, CA, USA) with RIN value > 7.0. The qualified RNA was then converted to cDNA for transcriptome sequencing performed on an Illumina HiSeq 2500 (Illumina, San Diego, CA, USA) at the CapitalBio Technology (Beijing, China). The raw sequences were filtered to remove the adapter sequences and contaminated reads. The retained mappable reads were aligned with the HISAT software program using the default parameters [33]. The rice genome sequence ENSEMBL release-31/IRGSP-1.0.31 was used as a reference [34].

4.5. Promoter-Luciferase Gene Expression Reporter Assay in N. benthamiana

The CDS of OsASR6 and the promotor region (2.0 kb upstream of the ATG) of CIPK15, WRKY45-1 and RAP2-13 were amplified using gene-specific primers listed in Supplemental Table S5. The CDS of OsASR6 was inserted after the 35S promoter of the effector vector pGWB5 while the promotor region of CIPK15, WRKY45-1 and RAP2-13 was inserted before the CDS of luciferase gene in the reporter vector pGWB435, respectively, using Gateway approach. The constructs were then individually transformed into Agrobacterium tumefaciens strain EHA105. The Agrobacterium carrying one of various fusion expression vectors (effector: pGWB5-GFP-OsASR6; reporters: pGWB435-CIPK15 p:LUC, pGWB435-WRKY45-1 p:LUC and pGWB435-RAP2-13 p:LUC) was cultured overnight at 28 °C, pelleted, and resuspended to OD600 of 0.3 (effector) or 0.1 (reporter) in infection buffer (10 mM MES, pH 5.6, 10 mM MgCl2, 150 μM acetosyringone). The bacterial suspensions of effector and reporter were mixed in 1:1 ratio and incubated for at least 1 h at room temperature in dark condition. The mixture was then infiltrated into one half of newly fully expanded leaf of N. benthamiana plant using a needleless syringe. As a control, the other half of leaf was infiltrated with mixture of EHA105 carrying the empty effector vector with GFP tag only and a reporter construct, respectively. At 36–48 h after infiltration, the abaxial sides of leaves were spread with 1mM luciferin (Promega) and the signal was captured using a Photek camera (HRPCS5; Photek).

4.6. Electrophoretic Mobility Shift Assay

For generation of OsASR6 protein, the cDNA sequence of OsASR6 was amplified through using gene-specific primers listed in Supplemental Table S5, and was then cloned into pET32a and expressed in Escherichia coli BL21 (DE3) pLysS (Trans-Gen Biotech). His-tagged OsASR6 protein was affinity purified and used for the electrophoretic mobility shift assay (EMSA). The biotinylated 4× GGCCCAT, 4× AGCCCAT and 4× GAAAAA probes as well as unlabeled versions of these sequences and mutated sequences were synthesized as forward and reverse strands, and were then renatured to double-stranded probes in annealing buffer [100 mM Tris-HCl, (pH 7.5), 10 mM EDTA, 1 M NaCl] at 100 °C for 5 min. The gel-shift assay was conducted according to the Thermo gel-shift assay system manual.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms23126622/s1.

Author Contributions

W.G. conducted the experiments; S.C. and Y.X. performed the transcriptome analyses; X.C. conceived and financially supported the study; X.C. and W.G. prepared the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the grants from Zhejiang Science and Technology Major Program on Agricultural New Variety Breeding (no. 2021C02064) and National Key Research and Development Project (no. 2014ZX0800905B).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare that they have no conflict of interest.

References

  1. Niño-Liu, D.O.; Ronald, P.C.; Bogdanove, A.J. Xanthomonas oryzae pathovars: Model pathogens of a model crop. Mol. Plant Pathol. 2006, 7, 303–324. [Google Scholar] [CrossRef] [PubMed]
  2. Yang, Y.; Zhou, Y.; Sun, J.; Liang, W.; Chen, X.; Wang, X.; Zhou, J.; Yu, C.; Wang, J.; Wu, S.; et al. Research progress on cloning and function of Xa genes against rice bacterial blight. Front. Plant Sci. 2022, 13, 847199. [Google Scholar] [CrossRef] [PubMed]
  3. Xie, X.; Chen, Z.; Cao, J.; Guan, H.; Lin, D.; Li, C.; Lan, T.; Duan, Y.; Mao, D.; Wu, W. Toward the positional cloning of Qblsr5a, a QTL underlying resistance to bacterial leaf streak, using overlapping sub-cssls in rice. PLoS ONE 2014, 9, e95751. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Triplett, L.R.; Cohen, S.P.; Heffelfinger, C.; Schmidt, C.; Huerta, A.I.; Tekete, C.; Verdier, V.; Bogdanove, A.J.; Leach, J.E. A resistance locus in the American heirloom rice variety Carolina Gold Select is triggered by TAL effectors with diverse predicted targets and is effective against African strains of Xanthomonas oryzae pv. oryzicola. Plant J. 2016, 87, 472–483. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Tao, Z.; Liu, H.; Qiu, D.; Zhou, Y.; Li, X.; Xu, C.; Wang, S.P. A pair of allelic WRKY genes play opposite roles in rice-bacteria interactions. Plant Physiol. 2009, 151, 936–948. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Shen, X.; Yuan, B.; Liu, H.; Li, X.; Xu, C.; Wang, S. Opposite functions of a rice mitogen-activated protein kinase during the process of resistance against Xanthomonas oryzae. Plant J. 2010, 64, 86–99. [Google Scholar] [CrossRef] [PubMed]
  7. Hui, S.; Shi, Y.; Tian, J.; Wang, L.; Li, Y.; Wang, S.; Yuan, M. TALE-carrying bacterial pathogens trap host nuclear import receptors for facilitation of infection of rice. Mol. Plant Pathol. 2019, 20, 519–532. [Google Scholar] [CrossRef]
  8. González, R.M.; Iusem, N.D. Twenty years of research on Asr (ABA stress-ripening) genes and proteins. Planta 2014, 239, 941–949. [Google Scholar] [CrossRef]
  9. Kim, S.J.; Lee, S.C.; Hong, S.K.; An, K.; An, G.; Kim, S.R. Ectopic expression of a cold responsive OsAsr1 cDNA gives enhanced cold tolerance in transgenic rice plants. Mol. Cells 2009, 27, 449–458. [Google Scholar] [CrossRef]
  10. Philippe, R.; Courtois, B.; McNally, K.L.; Mournet, P.; El-Malki, R.; Le Paslier, M.C.; Fabre, D. Structure, allelic diversity and selection of Asr genes, candidate for drought tolerance, in Oryza sativa L. and relatives. Theor. Appl. Genet. 2010, 121, 769–787. [Google Scholar] [CrossRef]
  11. Arenhart, R.A.; Yang, B.; Oliveira, L.F. New insights into aluminum tolerance in rice: The ASR5 protein binds the STAR1 promoter and other aluminum-responsive genes. Mol. Plant 2014, 7, 709–721. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Li, J.; Li, Y.; Yin, Z.; Jiang, J.; Zhang, M.; Guo, X.; Ye, Z. OsASR5 enhances drought tolerance through a stomatal closure pathway associated with ABA and H2O2 signaling in rice. Plant Biotechnol. J. 2017, 15, 183–196. [Google Scholar] [CrossRef] [PubMed]
  13. Li, N.; Wei, S.T.; Chen, J.; Yang, F.F.; Kong, L.G.; Chen, C.X.; Ding, X.H.; Chu, Z.H. OsASR2 regulates the expression of a defence-related gene, Os2H16, by targeting the GT-1 cis-element. Plant Biotechnol. J. 2018, 16, 771–783. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Shen, W.; Song, C.; Chen, J.; Fu, Y.; Wu, J.; Jiang, S. Transgenic rice plants harboring genomic DNA from Zizania latifolia confer bacterial blight resistance. Rice Sci. 2011, 18, 17–22. [Google Scholar] [CrossRef]
  15. Rom, S.; Gilad, A.; Kalifa, Y.; Konrad, Z.; Karpasas, M.M.; Goldgur, Y.; Bar-Zvi, D. Mapping the DNA- and zinc-binding domains of ASR1 (abscisic acid stress ripening), an abiotic-stress regulated plant specific protein. Biochimie 2006, 88, 621–628. [Google Scholar] [CrossRef]
  16. Kurusu, T.; Hamada, J.; Nokajima, H.; Kitagawa, Y.; Kiyoduka, M.; Takahashi, A.; Hanamata, S.; Ohno, R.; Hayashi, T.; Okada, K.; et al. Regulation of microbe-associated molecular pattern-induced hypersensitive cell death, phytoalexin production, and defense gene expression by calcineurin B-like protein-interacting protein kinases, OsCIPK14/15, in rice cultured cells. Plant Physiol. 2010, 153, 678–692. [Google Scholar] [CrossRef] [Green Version]
  17. Helliwell, E.E.; Wang, Q.; Yang, Y. Ethylene biosynthesis and signaling is required for rice immune response and basal resistance against Magnaporthe oryzae infection. Mol. Plant-Microbe Interact. 2016, 29, 831–843. [Google Scholar] [CrossRef] [Green Version]
  18. Zhu, J.; Huang, X.; Liu, T.; Gao, S.; Chen, J. Cloning and function analysis of a drought-inducible gene associated with resistance to Curvularia leaf spot in maize. Mol. Biol. Rep. 2012, 39, 7919–7926. [Google Scholar] [CrossRef]
  19. Liu, P.; Duan, Y.; Liu, C.; Xue, Q.; Guo, J.; Qi, T.; Kang, Z.; Guo, J. The calcium sensor TaCBL4 and its interacting protein TaCIPK5 are required for wheat resistance to stripe rust fungus. J. Exp. Bot. 2018, 69, 4443–4457. [Google Scholar] [CrossRef]
  20. Liu, P.; Guo, J.; Zhang, R.; Zhao, J.; Liu, C.; Qi, T.; Duan, Y.; Kang, Z.; Guo, J. TaCIPK10 interacts with and phosphorylates TaNH2 to activate wheat defense responses to stripe rust. Plant Biotechnol. J. 2019, 17, 956–968. [Google Scholar] [CrossRef]
  21. de la Torre, F.; Gutiérrez-Beltrán, E.; Pareja-Jaime, Y.; Chakravarthy, S.; Martin, G.B.; del Pozo, O. The tomato calcium sensor Cbl10 and its interacting protein kinase Cipk6 define a signaling pathway in plant immunity. Plant Cell 2013, 25, 2748–2764. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Yim, H.K.; Lim, M.N.; Lee, S.E.; Lim, J.; Lee, Y.; Hwang, Y.S. Hexokinase-mediated sugar signaling controls expression of the calcineurin B-like interacting protein kinase 15 gene and is perturbed by oxidative phosphorylation inhibition. J. Plant Physiol. 2012, 169, 1551–1558. [Google Scholar] [CrossRef] [PubMed]
  23. Liu, J.Q.; Chen, X.J.; Liang, X.X.; Zhou, X.G.; Yang, F.; Liu, J.; He, S.Y.; Guo, Z.J. Alternative splicing of rice WRKY62 and WRKY76 transcription factor genes in pathogen defense. Plant Physiol. 2016, 171, 1427–1442. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Wang, Z.X.; Yamanouchi, U.; Katayose, Y.; Sasaki, T.; Yano, M. Expression of the Pib rice-blast-resistance gene family is up-regulated by environmental conditions favoring infection and by chemical signals that trigger secondary plant defenses. Plant Mol. Biol. 2001, 47, 653–661. [Google Scholar] [CrossRef] [PubMed]
  25. Huang, H.C.; Thu, T.N.T.; He, X.H.; Gravot, A.; Bernillon, S.; Ballini, E.; Morel, J.B. Increase of fungal pathogenicity and role of plant glutamine in nitrogen-induced susceptibility (NIS) to rice blast. Front. Plant Sci. 2017, 8, 265. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Meteignier, L.V.; El, O.M.; Cohen, M.; Barff, T.; Matteau, D.; Lucier, J.F.; Rodrigue, S.; Jacques, P.E.; Yoshioka, K.; Moffett, P. Translatome analysis of an NB-LRR immune response identifies important contributors to plant immunity in Arabidopsis. J. Exp. Bot. 2017, 68, 2333–2344. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Koo, Y.J.; Kim, M.A.; Kim, E.H.; Song, J.T.; Jung, C.; Moon, J.K.; Kim, J.H.; Seo, H.S.; Song, S.I.; Kim, J.K.; et al. Overexpression of salicylic acid carboxyl methyltransferase reduces salicylic acid-mediated pathogen resistance in Arabidopsis thaliana. Plant Mol. Biol. 2007, 64, 1–15. [Google Scholar] [CrossRef]
  28. Zhou, J.; Peng, Z.; Long, J.; Sosso, D.; Liu, B.; Eom, J.S.; Huang, S.; Liu, S.; Vera Cruz, C.; Frommer, W.B.; et al. Gene targeting by the TAL effector PthXo2 reveals cryptic resistance gene for bacterial blight of rice. Plant J. 2015, 82, 632–643. [Google Scholar] [CrossRef]
  29. Livak, K.J.; Schmittgen, T.D. Analysis of relative gene expression data using real-time quantitative PCR. Methods 2001, 25, 402–408. [Google Scholar] [CrossRef]
  30. Li, W.; Xu, Y.P.; Zhang, Z.X.; Cao, W.Y.; Li, F.; Zhou, X.; Chen, G.Y.; Cai, X.Z. Identification of genes required for nonhost resistance to Xanthomonas oryzae pv. oryzae reveals novel signaling components. PLoS ONE 2012, 7, e42796. [Google Scholar]
  31. Kauffman, H.E.; Redd, A.P.K.; Hsiek, S.P.; Marca, S.D. An improved technique for evaluating resistance of race varieties to Xanthomonas oryzae. Plant Dis. Rep. 1973, 57, 537–541. [Google Scholar]
  32. Li, W.; Cao, J.Y.; Xu, Y.P.; Cai, X.Z. Artificial Agrobacterium tumefaciens strains exhibit diverse mechanisms to repress Xanthomonas oryzae pv. oryzae-induced hypersensitive response and nonhost resistance in Nicotiana benthamiana. Mol. Plant Pathol. 2017, 18, 489–502. [Google Scholar]
  33. Kim, D.; Langmead, B.; Salzberg, S.L. HISAT: A fast spliced aligner with low memory requirements. Nat. Methods 2015, 12, 357–360. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. The Rice Genome Sequence ENSEMBL Release-31/IRGSP-1.0.31. Available online: ftp://ftp.ensemblgenomes.org/pub/plants/release-31/fasta/oryza_sativa/dna/ (accessed on 3 February 2018).
Ijms 23 06622 g001 550
Figure 1. Expression of OsASR6 is strongly induced by Xoc and Xoo inoculations. WT-H2O, wild-type rice plants infiltrated with sterilized H2O; WT-Xoc, wild-type rice plants inoculated by leaf infiltration with Xoc strain oxy04 (OD600 = 1); WT-Xoo, wild-type rice plants inoculated by leaf clipping with Xoo strain PXO99 (OD600 = 1); The data obtained at 5 dpi were shown. The quantitative real-time PCR (qRT-PCR) experiments were conducted three times, each containing three replicates. The gene relative expression level was statistically analyzed using SPSS software. Significance of the differences between mean values was determined with Student’s t test. Error bars indicate SD, while asterisk (*) indicates significant difference at p < 0.05.
Figure 1. Expression of OsASR6 is strongly induced by Xoc and Xoo inoculations. WT-H2O, wild-type rice plants infiltrated with sterilized H2O; WT-Xoc, wild-type rice plants inoculated by leaf infiltration with Xoc strain oxy04 (OD600 = 1); WT-Xoo, wild-type rice plants inoculated by leaf clipping with Xoo strain PXO99 (OD600 = 1); The data obtained at 5 dpi were shown. The quantitative real-time PCR (qRT-PCR) experiments were conducted three times, each containing three replicates. The gene relative expression level was statistically analyzed using SPSS software. Significance of the differences between mean values was determined with Student’s t test. Error bars indicate SD, while asterisk (*) indicates significant difference at p < 0.05.
Ijms 23 06622 g001
Ijms 23 06622 g002 550
Figure 2. OsASR6 strongly negatively modulates rice resistance to Xoc. (A) Schematic representation of pANDA-OsASR6 vector. (B) OsASR6 gene expression of 5-week-old OsASR6-RNAi lines. (C) Rice bacterial leaf streak symptoms in WT and OsASR6-RNAi T2 lines at 10 d post inoculation (dpi) with Xoc strain oxy04 (OD600 = 1) by leaf infiltration method. Bar: 1 cm. (D) Statistical analysis of lesion length at 10 dpi. (E) Statistical analysis of bacterial level in planta at 10 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsASR6-RNAi lines (L) and those from wild-type plants (WT) (* p < 0.05).
Figure 2. OsASR6 strongly negatively modulates rice resistance to Xoc. (A) Schematic representation of pANDA-OsASR6 vector. (B) OsASR6 gene expression of 5-week-old OsASR6-RNAi lines. (C) Rice bacterial leaf streak symptoms in WT and OsASR6-RNAi T2 lines at 10 d post inoculation (dpi) with Xoc strain oxy04 (OD600 = 1) by leaf infiltration method. Bar: 1 cm. (D) Statistical analysis of lesion length at 10 dpi. (E) Statistical analysis of bacterial level in planta at 10 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsASR6-RNAi lines (L) and those from wild-type plants (WT) (* p < 0.05).
Ijms 23 06622 g002
Ijms 23 06622 g003 550
Figure 3. OsASR6 negatively modulates rice resistance to Xoo. (A) Rice bacterial blight symptoms in WT and OsASR6-RNAi T2 lines at 14 d post inoculation (dpi) with Xoo strain PXO99 (OD600 = 1) by leaf clipping method. Bar: 1 cm. (B) Statistical analysis of lesion length at 14 dpi. (C) Statistical analysis of bacterial level in planta at 14 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsASR6-RNAi lines (L) and those from wild-type plants (WT) (* p < 0.05).
Figure 3. OsASR6 negatively modulates rice resistance to Xoo. (A) Rice bacterial blight symptoms in WT and OsASR6-RNAi T2 lines at 14 d post inoculation (dpi) with Xoo strain PXO99 (OD600 = 1) by leaf clipping method. Bar: 1 cm. (B) Statistical analysis of lesion length at 14 dpi. (C) Statistical analysis of bacterial level in planta at 14 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsASR6-RNAi lines (L) and those from wild-type plants (WT) (* p < 0.05).
Ijms 23 06622 g003
Ijms 23 06622 g004 550
Figure 4. Identification of potential OsASR6 targets through transcriptome analyses. (A) Amino acid sequence alignment of OsASR6 with SlASR1 and OsASR2. The conserved ABA_WDS domain is overlined in black while the potential DNA-binding region is underlined in red. The identical and homologous amino acids are highlighted in blue and turquoise respectively. (B) Types of differentially expressed genes (DEGs). ASR6-RNAi/WT, comparison between un-inoculated OsASR6-RNAi and WT rice plants; ASR6-RNAi-Xoc/ASR6-RNAi-mock: comparison between Xoc-inoculated and mock-inoculated OsASR6-RNAi rice plants; WT-Xoc/WT-mock, comparison between Xoc-inoculated and mock-inoculated WT rice plants. (C) The strategies to identify constitutive and Xoc-responsive targets of OsASR6 function in suppressing rice resistance. Venn diagram showing the overlap between the Xoc-responsive genes in the WT and OsASR6-RNAi plants. The total number of overlapped DEGs is 742, among which 252 displayed reverse trend of Xoc-responsive expression in the WT and OsASR6-RNAi plants.
Figure 4. Identification of potential OsASR6 targets through transcriptome analyses. (A) Amino acid sequence alignment of OsASR6 with SlASR1 and OsASR2. The conserved ABA_WDS domain is overlined in black while the potential DNA-binding region is underlined in red. The identical and homologous amino acids are highlighted in blue and turquoise respectively. (B) Types of differentially expressed genes (DEGs). ASR6-RNAi/WT, comparison between un-inoculated OsASR6-RNAi and WT rice plants; ASR6-RNAi-Xoc/ASR6-RNAi-mock: comparison between Xoc-inoculated and mock-inoculated OsASR6-RNAi rice plants; WT-Xoc/WT-mock, comparison between Xoc-inoculated and mock-inoculated WT rice plants. (C) The strategies to identify constitutive and Xoc-responsive targets of OsASR6 function in suppressing rice resistance. Venn diagram showing the overlap between the Xoc-responsive genes in the WT and OsASR6-RNAi plants. The total number of overlapped DEGs is 742, among which 252 displayed reverse trend of Xoc-responsive expression in the WT and OsASR6-RNAi plants.
Ijms 23 06622 g004
Ijms 23 06622 g005 550
Figure 5. Quantitative real-time PCR validation of 10 potential OsASR6 target genes selected based on the transcriptome analysis. The relative gene expression pattern obtained from qRT-PCR experiments is shown in parallel with their gene expression pattern based on the transcriptome analysis for both comparisons WT-Xoc/WT-mock (A) and OsASR6-RNAi-Xoc/OsASR6-RNAi-mock (B). Total RNA was extracted from the Nipponbare plant leaves collected at 5 d post inoculation with Xoc strain oxy04 (OD600 = 1). The relative expression was plotted using the expression level of the TFIIAγ5 gene as a reference. Data were shown as the mean ± SD (n = 3). The relative expression level for none or insignificant differential expression in the transcriptome analysis was shown as zero.
Figure 5. Quantitative real-time PCR validation of 10 potential OsASR6 target genes selected based on the transcriptome analysis. The relative gene expression pattern obtained from qRT-PCR experiments is shown in parallel with their gene expression pattern based on the transcriptome analysis for both comparisons WT-Xoc/WT-mock (A) and OsASR6-RNAi-Xoc/OsASR6-RNAi-mock (B). Total RNA was extracted from the Nipponbare plant leaves collected at 5 d post inoculation with Xoc strain oxy04 (OD600 = 1). The relative expression was plotted using the expression level of the TFIIAγ5 gene as a reference. Data were shown as the mean ± SD (n = 3). The relative expression level for none or insignificant differential expression in the transcriptome analysis was shown as zero.
Ijms 23 06622 g005
Ijms 23 06622 g006 550
Figure 6. OsASR6 suppresses expression of CIPK15 but not WRKY45-1 and RAP2-13 in planta. Bioluminescence of Agrobacterium-mediated co-expression of GFP-OsASR6 (or GFP as control) and CIPK15 p:LUC (A) and WRKY45-1 p:LUC or RAP2-13 p:LUC (B) in N. benthamiana was detected 36 h–48 h after infiltration. Representative of three trials with similar results is shown. The bioluminescence intensity reporting the activity of luciferase (LUC) was quantified and the relative bioluminescence intensity of GFP-OsASR6 to GFP is shown. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between LUC-derived bioluminescence intensity affected by GFP-OsASR6 and that by GFP (* p < 0.05). Bar: 1 cm.
Figure 6. OsASR6 suppresses expression of CIPK15 but not WRKY45-1 and RAP2-13 in planta. Bioluminescence of Agrobacterium-mediated co-expression of GFP-OsASR6 (or GFP as control) and CIPK15 p:LUC (A) and WRKY45-1 p:LUC or RAP2-13 p:LUC (B) in N. benthamiana was detected 36 h–48 h after infiltration. Representative of three trials with similar results is shown. The bioluminescence intensity reporting the activity of luciferase (LUC) was quantified and the relative bioluminescence intensity of GFP-OsASR6 to GFP is shown. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between LUC-derived bioluminescence intensity affected by GFP-OsASR6 and that by GFP (* p < 0.05). Bar: 1 cm.
Ijms 23 06622 g006
Ijms 23 06622 g007 550
Figure 7. OsCIPK15 strongly positively modulates rice resistance to Xoc. (A) Schematic representation of pCZD-OsCIPK15 vector. (B) OsCIPK15 gene expression in 5-week-old OsCIPK15-OE lines. (C) Rice bacterial leaf streak symptoms in WT and OsCIPK15-OE T2 lines at 10 d post inoculation (dpi) with Xoc strain oxy04 (OD600 = 1) by leaf infiltration method. Bar: 1 cm. (D) Statistical analysis of lesion length at 10 dpi. (E) Statistical analysis of bacterial level in planta at 10 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsCIPK15-OE lines (L) and those from wild-type plants (WT) (* p < 0.05).
Figure 7. OsCIPK15 strongly positively modulates rice resistance to Xoc. (A) Schematic representation of pCZD-OsCIPK15 vector. (B) OsCIPK15 gene expression in 5-week-old OsCIPK15-OE lines. (C) Rice bacterial leaf streak symptoms in WT and OsCIPK15-OE T2 lines at 10 d post inoculation (dpi) with Xoc strain oxy04 (OD600 = 1) by leaf infiltration method. Bar: 1 cm. (D) Statistical analysis of lesion length at 10 dpi. (E) Statistical analysis of bacterial level in planta at 10 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsCIPK15-OE lines (L) and those from wild-type plants (WT) (* p < 0.05).
Ijms 23 06622 g007
Ijms 23 06622 g008 550
Figure 8. OsCIPK15 positively influences rice resistance to Xoo. (A) Rice bacterial blight symptoms in WT and OsCIPK15-OE T2 lines at 14 d post inoculation (dpi) with Xoo strain PXO99 (OD600 = 1) by leaf clipping method. Bar: 1 cm. (B) Statistical analysis of lesion length at 14 dpi. (C) Statistical analysis of bacterial level in planta at 14 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsCIPK15-OE lines (L) and those from wild-type plants (WT) (* p < 0.05).
Figure 8. OsCIPK15 positively influences rice resistance to Xoo. (A) Rice bacterial blight symptoms in WT and OsCIPK15-OE T2 lines at 14 d post inoculation (dpi) with Xoo strain PXO99 (OD600 = 1) by leaf clipping method. Bar: 1 cm. (B) Statistical analysis of lesion length at 14 dpi. (C) Statistical analysis of bacterial level in planta at 14 dpi. Data were analyzed by Student’s t-test and shown as the mean ± SD. Asterisks indicate significant difference between data from OsCIPK15-OE lines (L) and those from wild-type plants (WT) (* p < 0.05).
Ijms 23 06622 g008
Table
Table 1. Potential Xoc-responsive targets of OsASR6 function in suppressing rice resistance.
Table 1. Potential Xoc-responsive targets of OsASR6 function in suppressing rice resistance.
Gene IDLog2 FC Mean FPKM Value (ASR6-RNAi-Xoc/ASR6-RNAi-Mock)Log2 FC Mean FPKM Value (WT-Xoc/WT-Mock)Description
Defense response
OS08G05397002.53 (116.69/20.15)−2.00 (11.14/44.53)PibH8
OS03G02915001.94 (7.38/1.93)−4.36 (5.11/104.74)Asparagine synthetase 1
OS01G0206700−1.51 (11.32/32.23)1.40 (6.78/2.57)CIPK5
OS02G0627100−1.11 (0.36/0.77)6.53 (4.78/0.05)Phenylalanine ammonia-lyase 1
OS03G0300400−1.03 (1.48/3.03)4.36 (7.10/0.35)JIOsPR10
OS05G0127500−1.08 (0.90/1.91)1.25 (6.69/2.81)SRG1
OS01G0832300−1.76 (0.69/2.35)1.00 (1.41/0.70)Calcium-dependent protein kinase 3
Os10g0136500−1.68 (3.57/11.44)1.39 (21.76/8.28)Cysteine-rich receptor-like protein kinase 4
OS04G0220300−1.39 (2.26/5.90)1.47 (3.16/1.13)Wall-associated receptor kinase 2
OS11G0690332−1.27 (101.37/244.27)1.38 (265.24/101.92)Wall-associated receptor kinase 3-like
OS01G0123900−1.32 (78.73/196.81)2.03 (801.36/195.99)Bowman–Birk inhibitor 2-2
OS01G0124000−3.28 (2.86/27.89)3.18 (291.31/32.22)Bowman–Birk inhibitor 2-1
OS01G0220700−3.25 (0.59/5.61)2.64 (1.32/0.21)SWEET3b
OS05G0382600−2.44 (0.50/2.70)2.54 (11.6/2.00)Annexin D4
OS03G03489001.46 (2.04/0.74)−3.66 (1.10/13.82)E3 ubiquitin-protein ligase MIEL1
OS07G06180001.86 (4.59/1.27)−2.31 (1.12/5.85)E3 ubiquitin-protein ligase EL5
OS07G06646001.78 (16.22/4.72)−5.20 (0.50/18.31)Momilactone A synthase
OS01G0638600−1.85 (0.35/1.25)1.43 (0.82/0.31)Scopoletin glucosyltransferase
OS11G0113700/−1.69 (3.78/12.21)CIPK15
OS05G0322900/2.51 (340.84/59.71)WRKY45-1
OS09G0417600/1.85 (78.09/21.67)WRKY76
OS04G0578000/−1.60 (1.78/5.39)ACC synthase 2
OS12G0113500/−1.24 (6.54/15.50)CIPK14
OS01G0824600/−1.46 (2.21/6.08)CIPK11
OS12G0514500/−1.70 (35.94/116.94)Heat shock protein 90
OS01G0719100/−1.04 (94.80/195.14)RING zinc-finger protein 34
OS01G0699600/1.38 (2.73/1.05)NPK1-related protein kinase
OS07G01293001.30 (87.25/35.54)/Pathogenesis-related gene 1a
OS03G03206001.07 (4.12/1.96)/Calmodulin-binding protein 25
OS02G07873001.92 (80.25/21.22)/Mitogen-activated protein kinase kinase 5
OS01G0160800−1.14 (0.73/1.61)/Protein synthesis inhibitor I
OS11G0126100−2.55 (0.155/0.91)/Protein detoxification 21
OS03G0773700−1.88 (0.38/1.41)/BAM1
OS06G0587900−1.66 (1.05/3.31)/EMS1
OS02G08078001.51 (5.57/1.96)/Wall-associated receptor kinase 2
OS03G06883001.14 (9.73/4.42)/Calcium-dependent protein kinase 10
Hormone signaling
OS05G0102000−3.52 (0.05/0.57)2.73 (0.520.079)Jasmonic acid carboxyl methyltransferase 1
OS08G0360300−1.12 (1.33/2.90)3.20 (3.38/0.37)SARD1
OS08G0472800−1.50 (0.38/1.07)1.59 (5.53/1.84)ABA-8′-hydroxylase 2
OS10G0371100−2.37 (0.11/0.56)3.14 (0.83/0.09)RAP2-13
OS01G08838002.84 (15.37/2.15)−1.70 (18.12/59.03)Gibberellin 20 oxidase 2
OS02G0766700/1.24 (14.12/33.24)b-zip transcription factor 23
OS12G0116700/−2.10 (0.78/3.33)WRKY64
OS03G0758300/−1.17 (27.58/61.98)CNGC2
OS01G0701700/1.82 (2.60/0.73)Salicylate carboxymethyl transferase
OS02G06547001.42 (23.39/8.73)/Ethylene-responsive transcription factor 2
OS01G0190300−1.13 (0.82/1.79)/Auxin-responsive protein IAA2
OS02G06438001.15 (8.24/3.71)/SAUR36
OS03G01830002.28 (16.66/3.44)/ERF073
OS03G08601003.32 (0.84/0.08)/Ethylene-responsive transcription factor 15
Redox homeostasis
OS03G03489001.46 (2.04/0.74)−3.66 (1.10/13.82)Stress-related RING finger protein 1
OS01G0371200−1.63 (0.54/1.68)1.19 (1.40/0.61)GSTF1
OS02G0240300−1.01 (25.57/96.07)1.57 (229.94/61.97)Class III peroxidase 29
OS05G0412800−1.44 (0.27/0.73)1.65 (0.63/0.20)GST 23
OS07G0677400−1.05 (32.74/67.98)1.17 (111.37/49.35)Peroxidase 2
OS05G0323900/1.34 (302.17/119.05)Superoxide dismutase A1
OS03G02350002.38 (26.95/5.19)(26.9463/5.19005)/Peroxidase A2
“/”: no significant difference.
Table
Table 2. Potential constitutive targets of OsASR6 function in suppressing rice resistance.
Table 2. Potential constitutive targets of OsASR6 function in suppressing rice resistance.
Gene IDLog2 FC Mean FPKM Value (ASR6-RNAi/WT)p ValueRegulationDescription
Defense response
OS03G08567002.24 (1.11/5.25)0.00005downGibberellin 20 oxidase 1
OS01G0883800−4.68 (1.90/48.81)0.00005downGibberellin 20 oxidase 2
OS08G03603003.05 (2.90/0.350)0.00005upSARD1
OS03G03004003.19 (3.03/0.33)0.0016upJIOsPR10
OS01G03820002.13 (25.52/5.84)0.0001upPathogenesis-related gene 1b
OS01G0699600−2.15 (0.23/1.00)0.00945downNPK1-related protein kinase
OS02G0766700−2.20 (6.89/31.65)0.00005downBZIP23
OS02G06271003.97 (0.77/0.05)0.0047upPhenylalanine ammonia-lyase 1
OS03G0291500−5.69 (1.93/99.69)0.00005downASN1
OS01G08323001.81 (2.35/0.67)0.0001upCDPK3
OS03G06883002.45 (4.42/0.81)0.00005upCDPK10
OS01G02207004.79 (5.08/0.18)0.00025upSWEET3b
OS07G0618000−2.14 (1.27/5.57)0.00005downEL5
OS01G06386002.10 (1.25/0.29)0.00385upScopoletin glucosyltransferase
OS03G03206002.17 (1.96/0.44)0.00145upCalmodulin-binding protein 25
OS08G0539700−1.07 (20.15/42.38)0.0002downPibH8
OS01G0719100−1.05 (70.48/145.72)0.00015downRING zinc-finger protein 34
OS05G03229001.54 (165.62/57.04)0.00005upWRKY45-1
OS12G01167001.18 (7.58/3.35)0.00165upWRKY64
OS09G04176001.85 (74.77/20.69)0.00005upWRKY76
OS11G01261001.61 (0.91/0.30)0.0102upDetoxification 21
OS03G07737001.36 (1.90/0.74)0.00605upBAM1
OS01G02067003.84 (31.82/2.22)0.00005upCIPK5
OS01G0824600−1.21 (2.46/5.68)0.0003downCIPK11
OS12G0113500−1.80 (4.22/14.67)0.00005downCIPK14
OS11G0113700−2.18 (2.56/11.63)0.00005downCIPK15
OS12G0514500−1.90 (31.12/115.85)0.00005downHsp90
OS02G08078002.74 (1.95/0.29)0.00005upWall-associated receptor kinase 2
OS06G05879002.73 (2.60/0.39)0.00005upEMS1
Hormone signaling signaling
OS01G0741900−1.42 (69.90/186.71)0.00005downIAA6
OS02G0723400−1.38 (1.11/2.90)0.0028downIAA8
OS02G0703600−2.87 (2.05/15.00)0.00005downABA-8′-hydroxylase 1
OS08G0472800−1.24 (1.10/2.61)0.00745downABA-8′-hydroxylase 2
OS04G0546800−1.31 (65.01/161.00)0.00005downEthylene-responsive transcription factor 2
OS10G03711002.65 (0.56/0.09)0.01695upRAP2-13
OS03G01830001.03 (3.44/1.69)0.0064upERF073
OS07G0664600−1.89 (4.71/17.43)0.00055downRice microspore-preferred 8
OS05G01020002.93 (0.57/0.08)0.01505upJAMT1
OS01G07017001.64 (2.19/0.70)0.0017upSalicylate carboxymethyltransferase
OS04G0578000−2.69 (0.80/5.14)0.00005downACS2
Redox homeostasis
OS06G0727200−1.71 (18.86/61.50)0.00005downCatalase isozyme B
OS07G0665200−1.50 (144.55/409.77)0.00005downSuperoxide dismutase 2
OS07G0694600−2.59 (130.59/788.56)0.00005downAPX2
OS07G0616500−1.34 (9.00/22.76)0.00005downGLO4
OS03G0348900−4.14 (0.74/13.14)0.00005downStress-related RING finger protein 1
OS07G0677600−2.16 (2.01/8.96)0.00005downCationic peroxidase 1
OS01G03712001.47 (1.62/0.58)0.03705upGSTF1
OS05G03046001.08 (74.34/35.16)0.00005upLipoxygenase 6
OS02G05377001.27 (520.38/215.89)0.00005upBAS1
OS10G05366001.10 (1.22/0.57)0.03295upPeroxidase 5
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Guo, W.; Chen, S.; Xu, Y.; Cai, X. OsASR6 Alleviates Rice Resistance to Xanthomonas oryzae via Transcriptional Suppression of OsCIPK15. Int. J. Mol. Sci. 2022, 23, 6622. https://doi.org/10.3390/ijms23126622

AMA Style

Guo W, Chen S, Xu Y, Cai X. OsASR6 Alleviates Rice Resistance to Xanthomonas oryzae via Transcriptional Suppression of OsCIPK15. International Journal of Molecular Sciences. 2022; 23(12):6622. https://doi.org/10.3390/ijms23126622

Chicago/Turabian Style

Guo, Weiyi, Songyu Chen, Youping Xu, and Xinzhong Cai. 2022. "OsASR6 Alleviates Rice Resistance to Xanthomonas oryzae via Transcriptional Suppression of OsCIPK15" International Journal of Molecular Sciences 23, no. 12: 6622. https://doi.org/10.3390/ijms23126622

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop