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Home > Archive>Volume 18, Issue 2, 2017 >298-309. DOI:10.13430/j.cnki.jpgr.2017.02.016 Online First
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Resistance spectrum against Xanthomonas oryzae pv. oryzae and RNA-seq analysis of the introgression line W6023 derived from cross between oryza rufipogon and cultivated rice
DOI:
10.13430/j.cnki.jpgr.2017.02.016
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  • ZHANG Mingwei

    ZHANG Mingwei

    Institute of Crop Sciences,Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement
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  • XU Feifei

    XU Feifei

    Institute of Crop Sciences,Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement
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  • HAO Wei

    HAO Wei

    Institute of Crop Sciences,Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement
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  • WANG Chunlian

    WANG Chunlian

    Institute of Crop Sciences,Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement
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  • ZHAO Kaijun

    ZHAO Kaijun

    Institute of Crop Sciences,Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement
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    Abstract:

    Rice bacterial blight (BB) is a worldwide rice disease devastating rice yield seriously. In order to explore new resistance genes against BB, we investigated resistance spectrum of W6023, an introgression line derived from cross between o.rufipogon and cultivated rice. Inoculation assays showed that W6023 was highly resistant to 23 of the 25 Xanthomonas oryzae pv. Oryzae (Xoo) strains tested, and the broad resistance spectrum is different from those conferred by other known BB resistance genes. Subsequently, W6023 and its susceptible recurrent parent IR24 were in?ltrated with the broadly virulent Xoo strain PXO99(P6) and RNA-seq analysis was performed. Totally 105644962 and 91022599 sequences were obtained from W6023 and IR24, respectively. GO annotation and KEGG enrichment analysis revealed differentially expressed genes (DEGs) mainly enriched in biosynthesis of secondary metabolites, plant hormone signal transduction and starch & sucrose metabolism. Among these differentially expressed genes, there were 203 significantly differentially expressed genes, of which 114 genes (56.2%) were up-regulated and 89 (43.8%) down-regulated in W6023, and 35.9% of them were located on chromosome 11. Bioinformatics analysis showed that 16 out of the 203 differentially expressed genes belonged to disease resistance genes such as NBS-LRR or receptor kinases; 14 genes were directly or indirectly associated with metabolism of peroxides in rice, encoding peroxidase, metallothionein, and so on; 6 genes encode resistance-related transcription factors, such as WRKY and NAC; 18 signal transduction-related genes encode calmodulin binding proteins, terpene synthase, glucosyltransferase, and so on. Six up-regulated genes of W6023 and three up-regulated genes of IR24 were randomly selected and analyzed by RT-PCR and qRT-PCR. The results were consistent with the data of transcriptome sequencing, indicating that the transcriptome data obtained in this study were reliable. These above results provide a basis for the further isolation of resistance genes in W6023.

    Key words:rice; resistance gene; bacterial blight; transcriptome sequencing; differentially expressed genes
    Reference
    [1] Mew T. Current status and future prospects of research on bacterial blight of rice [J]. Annual review of phytopathology, 1987, 25(1): 359-382.
    [2] Nino-Liu D O, Ronald P C, Bogdanove A J. Xanthomonas oryzae pathovars: model pathogens of a model crop [J]. Mol Plant Pathol, 2006, 7(5): 303-324.
    [3] 姬广海, 张世光, 钱君. 云南水稻白叶枯病菌生理小种初析 [J]. 植物保护, 2003, 29(1): 19-21.
    [4] 曾列先, 朱小源, 杨健源, 等. 广东水稻白叶枯病菌新致病型的发现及致病性测定 [J]. 广东农业科学, 2005, (2): 58-59.
    [5] Brown J W, Calixto C P, Zhang R. High‐quality Reference transcript datasets hold the key to transcript‐specific RNA‐sequencing analysis in plants [J]. New Phytologist, 2016, (9): 1-5.
    [6] Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics [J]. Nature reviews genetics, 2009, 10(1): 57-63.
    [7] Kim K H, Kang Y J, Kim D H, et al. RNA-Seq analysis of a soybean near-isogenic line carrying bacterial leaf pustule-resistant and-susceptible alleles [J]. DNA research, 2011, 18(6): 483-497.
    [8] Xu L, Zhu L, Tu L, et al. Lignin metabolism has a central role in the resistance of cotton to the wilt fungus Verticillium dahliae as revealed by RNA-Seq-dependent transcriptional analysis and histochemistry [J]. Journal of experimental botany, 2011, 62(15): 5607-5621.
    [9] Strau? T, Van Poecke R M, Strau? A, et al. RNA-seq pinpoints a Xanthomonas TAL-effector activated resistance gene in a large-crop genome [J]. Proceedings of the National Academy of Sciences, 2012, 109(47): 19480-19485.
    [10] Yang K, Rong W, Qi L, et al. Isolation and characterization of a novel wheat cysteine-rich receptor-like kinase gene induced by Rhizoctonia cerealis [J]. Scientific reports, 2013, 3(3): 255-266.
    [11] He B, Tao X, Gu Y, et al. Transcriptomic Analysis and the Expression of Disease-Resistant Genes in Oryza meyeriana under Native Condition [J]. PloS one, 2015, 10(12): e0144518.
    [12] Wang C, Fan Y, Zheng C, et al. High-resolution genetic mapping of rice bacterial blight resistance gene Xa23 [J]. Molecular Genetics and Genomics, 2014, 289(5): 745-753.
    [13] Kauffman H, Reddy A, Hsieh S, et al. Improved technique for evaluating resistance of rice varieties to Xanthomonas oryzae [J]. Plant Disease Reporter, 1973, ( 57): 537-541.
    [14] Amante-Bordeos A, Sitch L, Nelson R, et al. Transfer of bacterial blight and blast resistance from the tetraploid wild rice Oryza minuta to cultivated rice, Oryza sativa [J]. Theoretical and Applied Genetics, 1992, 84(3-4): 345-354.
    [15] Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2? ΔΔCT method [J]. methods, 2001, 25(4): 402-408.
    [16] Gu K, Tian D, Yang F, et al. High-resolution genetic mapping of Xa27 (t), a new bacterial blight resistance gene in rice, Oryza sativa L [J]. Theoretical and Applied Genetics, 2004, 108(5): 800-807.
    [17] Choisne N, Demange N, Orjeda G, et al. The sequence of rice chromosomes 11 and 12, rich in disease resistance genes and recent gene duplications [J]. BMC biology, 2005, 3(1): 20.
    [18] Zipfel C, Rathjen J P. Plant immunity: AvrPto targets the frontline [J]. Current Biology, 2008, 18(5): 218-220.
    [19] Fukuoka S, Yamamoto S-I, Mizobuchi R, et al. Multiple functional polymorphisms in a single disease resistance gene in rice enhance durable resistance to blast [J]. Scientific Reports, 2014, 4(4): 4550.
    [20] Yoshimura S, Yamanouchi U, Katayose Y, et al. Expression of Xa1, a bacterial blight-resistance gene in rice, is induced by bacterial inoculation [J]. Proceedings of the National Academy of Sciences, 1998, 95(4): 1663-1668.
    [21] Stone J M, Walker J C. Plant protein kinase families and signal transduction [J]. Plant Physiology, 1995, 108(2): 451-457.
    [22] Chen X, Ronald P C. Innate immunity in rice [J]. Trends in plant science, 2011, 16(8): 451-459.
    [23] Liu B, Li J-F, Ao Y, et al. Lysin motif–containing proteins LYP4 and LYP6 play dual roles in peptidoglycan and chitin perception in rice innate immunity [J]. The Plant Cell, 2012, 24(8): 3406-3419.
    [24] Song W-Y, Pi L-Y, Wang G-L, et al. Evolution of the rice Xa21 disease resistance gene family [J]. The Plant Cell, 1997, 9(8): 1279-1287.
    [25] Kawasaki T, Nam J, Boyes D C, et al. A duplicated pair of arabidopsis RING‐finger E3 ligases contribute to the RPM1‐and RPS2‐mediated hypersensitive response [J]. The Plant Journal, 2005, 44(2): 258-270.
    [26] Joseph L M, Koon T T, Man W S. Antifungal effects of hydrogen peroxide and peroxidase on spore germination and mycelial growth of Pseudocercospora species [J]. Canadian Journal of Botany, 1998, 76(12): 2119-2124.
    [27] Bai H, Lan J P, Gan Q, et al. Identification and expression analysis of components involved in rice Xa21-mediated disease resistance signalling [J]. Plant Biol (Stuttg), 2012, 14(6): 914-922.
    [28] Kao C-W, Bakshi M, Sherameti I, et al. A Chinese cabbage (Brassica campetris subsp. Chinensis) τ-type glutathione-S-transferase stimulates Arabidopsis development and primes against abiotic and biotic stress [J]. Plant Molecular Biology, 2016, 92(6): 643-659.
    [29] Jin S, Sun D, Wang J, et al. Expression of the rgMT gene, encoding for a rice metallothionein-like protein in Saccharomyces cerevisiae and Arabidopsis thaliana [J]. Journal of genetics, 2014, 93(3): 709-718.
    [30] Cho H Y, Lee C, Hwang S-G, et al. Overexpression of the OsChI1 gene, encoding a putative laccase precursor, increases tolerance to drought and salinity stress in transgenic Arabidopsis [J]. Gene, 2014, 552(1): 98-105.
    [31] Cheng H, Liu H, Deng Y, et al. The WRKY45-2 WRKY13 WRKY42 transcriptional regulatory cascade is required for rice resistance to fungal pathogen [J]. Plant physiology, 2015, 167(3): 1087-1099.
    [32] Liu J, Chen X, Liang X, et al. Alternative splicing of rice WRKY62 and WRKY76 transcription factor genes in pathogen defense [J]. Plant physiology, 2016, 171(2): 1427-1442.
    [33] Nuruzzaman M, Manimekalai R, Sharoni A M, et al. Genome-wide analysis of NAC transcription factor family in rice [J]. Gene, 2010, 465(1): 30-44.
    [34] 孙利军, 李大勇, 张慧娟, 等. NAC 转录因子在植物抗病和抗非生物胁迫反应中的作用 [J]. 遗传, 2012, 34(8): 993-1002.
    [35] Wang F, Lin R, Feng J, et al. TaNAC1 acts as a negative regulator of stripe rust resistance in wheat, enhances susceptibility to Pseudomonas syringae, and promotes lateral root development in transgenic Arabidopsis thaliana [J]. Frontiers in plant science, 2015, 6(108): 1-15.
    [36] Grand X, Espinoza R, Michel C, et al. Identification of positive and negative regulators of disease resistance to rice blast fungus using constitutive gene expression patterns [J]. Plant biotechnology journal, 2012, 10(7): 840-850.
    [37] Zheng X, Chen X, Zhang X, et al. Isolation and identification of a gene in response to rice blast disease in rice [J]. Plant molecular biology, 2004, 54(1): 99-109.
    [38] Rao S S, El‐Habbak M H, Havens W M, et al. Overexpression of GmCaM4 in soybean enhances resistance to pathogens and tolerance to salt stress [J]. Molecular plant pathology, 2014, 15(2): 145-160.
    [39] Taniguchi S, Miyoshi S, Tamaoki D, et al. Isolation of jasmonate-induced sesquiterpene synthase of rice: product of which has an antifungal activity against Magnaporthe oryzae [J]. Journal of plant physiology, 2014, 171(8): 625-632.
    [40] Yoshitomi K, Taniguchi S, Tanaka K, et al. Rice terpene synthase 24 (OsTPS24) encodes a jasmonate-responsive monoterpene synthase that produces an antibacterial γ-terpinene against rice pathogen [J]. Journal of plant physiology, 2016, (191): 120-126.
    [41] Dixon R A. Natural products and plant disease resistance [J]. Nature, 2001, 411(6839): 843-847.
    [42] 林凡云, 陆琼娴, 徐剑宏, 等. 两个与盐和赤霉病菌胁迫相关的小麦糖基转移酶基因的克隆与表达 [J]. 遗传, 2008, 30(12): 1608-1614.
    [43] Langlois-Meurinne M, Gachon C M, Saindrenan P. Pathogen-responsive expression of glycosyltransferase genes UGT73B3 and UGT73B5 is necessary for resistance to Pseudomonas syringae pv tomato in Arabidopsis [J]. Plant physiology, 2005, 139(4): 1890-1901.
    [44] Simon C, Langlois‐Meurinne M, Didierlaurent L, et al. The secondary metabolism glycosyltransferases UGT73B3 and UGT73B5 are components of redox status in resistance of Arabidopsis to Pseudomonas syringae pv. tomato [J]. Plant, cell environment, 2014, 37(5): 1114-1129.
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History
  • Received:November 27,2016
  • Revised:December 12,2016
  • Adopted:December 27,2016
  • Online: March 14,2017
  • Published:
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