Nemhauser JL, Hong F, Chory J. Different plant hormones regulate similar processes through largely nonoverlapping transcriptional responses. Cell. 2006;126:467–75.
Article
CAS
PubMed
Google Scholar
Miller CO, Skoog F, Okomura FS, von Saltza MH, Strong FM. Isolation, structure and synthesis of kinetin, a substance promoting cell division. J Am Chem Soc. 1956;78:1345–50.
Google Scholar
Miller CO, Skoog F, Von Saltza MH, Strong F. Kinetin, a cell division factor from deoxyribonucleic acid. J Am Chem Soc. 1955;77:1392.
Article
CAS
Google Scholar
Argueso CT, Ferreira FJ, Kieber JJ. Environmental perception avenues: the interaction of cytokinin and environmental response pathways. Plant Cell Environ. 2009;32:1147–60.
Article
CAS
PubMed
Google Scholar
Mok DW, Mok MC. Cytokinin metabolism and action. Annu Rev Plant Physiol Plant Mol Biol. 2001;89:89–118.
Article
Google Scholar
Kieber JJ, Schaller GE. Cytokinins. Arabidopsis Book. 2014;12:e0168.
Article
PubMed
PubMed Central
Google Scholar
Frugier F, Kosuta S, Murray JD, Crespi M, Szczyglowski K. Cytokinin: secret agent of symbiosis. Trends Plant Sci. 2008;13:115–20.
Article
CAS
PubMed
Google Scholar
Giulini A, Wang J, Jackson D. Control of phyllotaxy by the cytokinin-inducible response regulator homologue ABPHYL1. Nature. 2004;430:1031–4.
Article
CAS
PubMed
Google Scholar
Caesar K, Thamm AMK, Witthöft J, Elgass K, Huppenberger P, Grefen C, Horak J, Harter K. Evidence for the localization of the Arabidopsis cytokinin receptors AHK3 and AHK4 in the endoplasmic reticulum. J Exp Bot. 2011;62:5571–80.
Article
CAS
PubMed
PubMed Central
Google Scholar
Lomin SN, Yonekura-Sakakibara K, Romanov GA, Sakakibara H. Ligand-binding properties and subcellular localization of maize cytokinin receptors. J Exp Bot. 2011;62:5149–59.
Article
CAS
PubMed
PubMed Central
Google Scholar
Inoue T, Higuchi M, Hashimoto Y, Seki M, Kobayashi M, Kato T, Tabata S, Shinozaki K, Kakimoto T. Identification of CRE1 as a cytokinin receptor from Arabidopsis. Nature. 2001;409:1060–3.
Article
CAS
PubMed
Google Scholar
Ueguchi C, Sato S, Kato T, Tabata S. The AHK4 gene involved in the cytokinin-signaling pathway as a direct receptor molecule in Arabidopsis thaliana. Plant Cell Physiol. 2001;42:751–5.
Article
CAS
PubMed
Google Scholar
Suzuki T, Miwa K, Ishikawa K, Yamada H, Aiba H, Mizuno T. The Arabidopsis sensor His-kinase, AHK4, can respond to cytokinins. Plant Cell Physiol. 2001;42:107–13.
Article
CAS
PubMed
Google Scholar
Yamada H, Suzuki T, Terada K, Takei K, Ishikawa K, Miwa K, Yamashino T, Mizuno T. The Arabidopsis AHK4 histidine kinase is a cytokinin-binding receptor that transduces cytokinin signals across the membrane. Plant Cell Physiol. 2001;41:1017–23.
Article
Google Scholar
Hutchison CE, Li J, Argueso C, Gonzalez M, Lee E, Lewis MW, Maxwell BB, Perdue TD, Schaller GE, Alonso JM, et al. The Arabidopsis histidine phosphotransfer proteins are redundant positive regulators of cytokinin signaling. Plant Cell. 2006;18:3073–87.
Article
CAS
PubMed
PubMed Central
Google Scholar
Punwani JA, Hutchison CE, Schaller GE, Kieber JJ. The subcellular distribution of the Arabidopsis Histidine Phosphotransfer proteins is independent of cytokinin signaling. Plant J. 2010;62:473–82.
Article
CAS
PubMed
Google Scholar
Mason MG, Mathews DE, Argyros DA, Maxwell BB, Kieber JJ, Alonso JM, Ecker JRS, Schaller GE. Multiple type-B response regulators mediate cytokinin signal transduction in Arabidopsis. Plant Cell. 2005;17:3007–18.
Article
CAS
PubMed
PubMed Central
Google Scholar
Ishida K, Yamashino T, Mizuno T. Expression of the cytokinin-induced type-A response regulator gene ARR9 is regulated by the circadian clock in Arabidopsis thaliana. Biosci Biotechnol Biochem. 2008;72:3025–9.
Article
CAS
PubMed
Google Scholar
Yokoyama A, Yamashino T, Amano Y, Tajima Y, Imamura A, Sakakibara H, Mizuno T. Type-B ARR transcription factors, ARR10 and ARR12, are implicated in cytokinin-mediated regulation of protoxylem differentiation in roots of Arabidopsis thaliana. Plant Cell Physiol. 2007;48:84–96.
Article
CAS
PubMed
Google Scholar
Argyros RD, Mathews DE, Chiang YH, Palmer CM, Thibault DM, Etheridge N, Argyros DA, Mason MG, Kieber JJ, Schaller GE. Type B response regulators of Arabidopsis play key roles in cytokinin signaling and plant development. Plant Cell. 2008;20:2102–16.
Article
CAS
PubMed
PubMed Central
Google Scholar
To JP, Deruère J, Maxwell BB, Morris VF, Hutchison CE, Schaller GE, Kieber JJ. Cytokinin regulates type-A Arabidopsis response regulator activity and protein stability via two-component phosphorelay. Plant Cell. 2007;19:3901–14.
Article
CAS
PubMed
PubMed Central
Google Scholar
To JPC, Haberer G, Ferreira FJ, Deruère J, Mason MG, Schaller GE, Alonso JM, Ecker JR, Kieber JJ. Type-A ARRs are partially redundant negative regulators of cytokinin signaling in Arabidopsis. Plant Cell. 2004;16:658–71.
Article
CAS
PubMed
PubMed Central
Google Scholar
Brandstatter I, Kieber JJ. Two genes with similarity to bacterial response regulators are rapidly and specifically induced by cytokinin in Arabidopsis. Plant Cell. 1998;10:1009–20.
Article
CAS
PubMed
PubMed Central
Google Scholar
D'Agostino I, Deruère J, Kieber JJ. Characterization of the response of the Arabidopsis ARR gene family to cytokinin. Plant Physiol. 2000;124:1706–17.
Article
PubMed
PubMed Central
Google Scholar
Mohanty S. Trends in global rice consumption. Rice Today. 2013;12:44–5.
Google Scholar
Ashikari M, Sakakibara H, Lin S, Yamamoto T, Takashi T, Nishimura A, Angeles ER, Qian Q, Kitano H, Matsuoka M. Cytokinin oxidase regulates rice grain production. Science. 2005;309:741–5.
Article
CAS
PubMed
Google Scholar
Tsai YC, Weir N, Hill K, Zhang W, Kim HJ, Shiu SH, Schaller E, Kieber JJ. Characterization of genes involved in cytokinin signaling and metabolism from rice. Plant Physiol. 2012;158:1666–84.
Article
CAS
PubMed
PubMed Central
Google Scholar
Du L, Jiao F, Chu J, Jin G, Chen M, Wu P. The two-component signal system in rice (Oryza sativa L.): A genome-wide study of cytokinin signal perception and transduction. Genomics. 2007;89:697–707.
Article
CAS
PubMed
Google Scholar
Schaller GE, Doi K, Hwang I, Kieber JJ, Khurana JP, Kurata N, Mizuno T, Pareek A, Shiu S-H, Wu P, et al. Nomenclature for two-component signaling elements of rice. Plant Physiol. 2007;143:555–7.
Article
CAS
PubMed
PubMed Central
Google Scholar
Choi J, Lee J, Kim K, Cho M, Ryu H, An G, Hwang I. Functional identification of OsHk6 as a homotypic cytokinin receptor in rice with preferential affinity for iP. Plant Cell Physiol. 2012;53:1334–43.
Article
CAS
PubMed
Google Scholar
Sun L, Zhang Q, Wu J, Zhang L, Jiao X, Zhang S, Zhang Z, Sun D, Lu T, Sun Y. Two rice authentic histidine phosphotransfer proteins, OsAHP1 and OsAHP2, mediate cytokinin signaling and stress responses in rice. Plant Physiol. 2014;165:335–45.
Article
CAS
PubMed
PubMed Central
Google Scholar
Hirose N, Makita N, Kojima M, Kamada-Nobusada T, Sakakibara H. Overexpression of a type-A response regulator alters rice morphology and cytokinin metabolism. Plant Cell Physiol. 2007;48:523–39.
Article
CAS
PubMed
Google Scholar
Cheng X, Jiang H, Zhang J, Qian Y, Zhu S, Cheng B. Overexpression of type-A rice response regulators, OsRR3 and OsRR5, results in lower sensitivity to cytokinins. Genet Mol Res. 2010;9:348–59.
Article
CAS
PubMed
Google Scholar
Rashotte AM, Carson SD, To JP, Kieber JJ. Expression profiling of cytokinin action in Arabidopsis. Plant Physiol. 2003;132:1998–2011.
Article
CAS
PubMed
PubMed Central
Google Scholar
Brenner WG, Romanov GA, Kollmer I, Burkle L, Schmülling T. Immediate-early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome-wide expression profiling reveal novel cytokinin-sensitive processes and suggest cytokinin action through transcriptional cascades. Plant J. 2005;44:314–33.
Article
CAS
PubMed
Google Scholar
Kiba T, Naitou T, Koizumi N, Yamashino T, Sakakibara H, Mizuno T. Combinatorial microarray analysis revealing Arabidopsis genes implicated in cytokinin responses through the His->Asp phosphorelay circuitry. Plant Cell Physiol. 2005;46:339–55.
Article
CAS
PubMed
Google Scholar
Bhargava A, Clabaugh I, To JP, Maxwell BB, Chiang YH, Schaller GE, Loraine A, Kieber JJ. Identification of cytokinin-responsive genes using microarray meta-analysis and RNA-Seq in Arabidopsi. Plant Physiol. 2013;162:272–94.
Article
CAS
PubMed
PubMed Central
Google Scholar
Brenner WG, Schmülling T. Transcript profiling of cytokinin action in Arabidopsis roots and shoots discovers largely similar but also organ-specific responses. BMC Plant Biol. 2012;12:112.
Article
CAS
PubMed
PubMed Central
Google Scholar
Nicol JW, Helt GA, Blanchard SGJ, Raja A, Loraine AE. The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets. Bioinformatics. 2009;25:2730–1.
Article
CAS
PubMed
PubMed Central
Google Scholar
Kawahara Y, de la Bastide M, Hamilton J, Kanamori H, McCombie W, Ouyang S, Schwartz D, Tanaka T, Wu J, Zhou S, et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data. Rice. 2013;6:4.
Article
PubMed
Google Scholar
Sakai H, Lee SS, Tanaka T, Numa H, Kim J, Kawahara Y, Wakimoto H, Yang CC, Iwamoto M, Abe T, et al. Rice annotation project database (RAP-DB): An integrative and interactive database for rice genomics. Plant Cell Physiol. 2013;54:e6.
Article
CAS
PubMed
PubMed Central
Google Scholar
Ramsköld D, Wang ET, Burge CB, Sandberg R. An abundance of ubiquitously expressed genes revealed by tissue transcriptome sequence data. PLoS Comput Biol. 2009;5:e1000598.
Article
PubMed
PubMed Central
Google Scholar
Loraine AE, McCormick S, Estrada A, Patel K, Qin P. RNA-seq of Arabidopsis pollen uncovers novel transcription and alternative splicing. Plant Physiol. 2013;162:1092–109.
Article
CAS
PubMed
PubMed Central
Google Scholar
Cobbett C, Goldsbrough P. Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis. Annu Rev Plant Biol. 2002;53:159–82.
Article
CAS
PubMed
Google Scholar
Geiss GK, Bumgarner RE, Birditt B, Dahl T, Dowidar N, Dunaway DL, Fell HP, Ferree S, George RD, Grogan T, et al. Direct multiplexed measurement of gene expression with color-coded probe pairs. Nat Biotech. 2008;26:317–25.
Article
CAS
Google Scholar
Malkov V, Serikawa K, Balantac N, Watters J, Geiss G, Mashadi-Hossein A, Fare T. Multiplexed measurements of gene signatures in different analytes using the Nanostring nCounterTM Assay System. BMC Res Notes. 2009;2:80.
Article
PubMed
PubMed Central
Google Scholar
Jin J, Zhang H, Kong L, Gao G, Luo J. PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors. Nucleic Acids Res. 2014;42:D1182–7.
Article
CAS
PubMed
Google Scholar
Werner T, Motyka V, Strnad M, Schmülling T. Regulation of plant growth by cytokinin. Proc Natl Acad Sci U S A. 2001;98:10487–92.
Article
CAS
PubMed
PubMed Central
Google Scholar
Hayakawa T, Kudo T, Ito T, Takahashi N, Yamaya T. ACT domain repeat protein 7, ACR7, interacts with a chaperone HSP18.0-CII in rice nuclei. Plant Cell Physiol. 2006;47:891–904.
Article
CAS
PubMed
Google Scholar
Nakagawa M, Shimamoto K, Kyozuka J. Overexpression of RCN1 and RCN2, rice TERMINAL FLOWER 1/CENTRORADIALIS homologs, confers delay of phase transition and altered panicle morphology in rice. Plant J. 2002;29:743–50.
Article
CAS
PubMed
Google Scholar
Li L, Stoeckert CJ, Roos DS. OrthoMCL: Identification of ortholog groups for eukaryotic genomes. Genome Res. 2003;13:2178–89.
Article
CAS
PubMed
PubMed Central
Google Scholar
Hosoda K, Imamura A, Katoh E, Hatta T, Tachiki M, Yamada H, Mizuno T, Yamazaki T. Molecular structure of the GARP family of plant Myb-related DNA binding motifs of the Arabidopsis response regulators. Plant Cell. 2002;14:2015–29.
Article
CAS
PubMed
PubMed Central
Google Scholar
Sakai H, Aoyama T, Oka A. Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators. Plant J. 2000;24:703–11.
Article
CAS
PubMed
Google Scholar
Imamura A, Kiba T, Tajima Y, Yamashino T, Mizuno T. In vivo and in vitro characterization of the ARR11 response regulator implicated in the His-to-Asp phosphorelay signal transduction in Arabidopsis thaliana. Plant Cell Physiol. 2003;44:122–31.
Article
CAS
PubMed
Google Scholar
Taniguchi M, Sasaki N, Tsuge T, Aoyama T, Oka A. ARR1 directly activates cytokinin response genes that encode proteins with diverse regulatory functions. Plant Cell Physiol. 2007;48:263–77.
Article
CAS
PubMed
Google Scholar
Zürcher E, Tavor-Deslex D, Lituiev D, Enkerli K, Tarr PT, Müller B. A robust and sensitive synthetic sensor to monitor the transcriptional output of the cytokinin signaling network in planta. Plant Physiol. 2013;161:1066–75.
Article
PubMed
PubMed Central
Google Scholar
Franco-Zorrilla JM, López-Vidriero I, Carrasco JL, Godoy M, Vera P, Solano R. DNA-binding specificities of plant transcription factors and their potential to define target genes. Proc Natl Acad Sci U S A. 2014;111:2367–72.
Article
CAS
PubMed
PubMed Central
Google Scholar
Weirauch Matthew T, Yang A, Albu M, Cote AG, Montenegro-Montero A, Drewe P, Najafabadi Hamed S, Lambert Samuel A, Mann I, Cook K, et al. Determination and inference of eukaryotic transcription factor sequence specificity. Cell. 2014;158:1431–43.
Article
CAS
PubMed
PubMed Central
Google Scholar
Godoy M, Franco-Zorrilla JM, Pérez-Pérez J, Oliveros JC, Lorenzo Ó, Solano R. Improved protein-binding microarrays for the identification of DNA-binding specificities of transcription factors. Plant J. 2011;66:700–11.
Article
CAS
PubMed
Google Scholar
Schoor S, Farrow S, Blaschke H, Lee S, Perry G, von Schwartzenberg K, Emery N, Moffatt B. Adenosine kinase contributes to cytokinin interconversion in Arabidopsis. Plant Physiol. 2011;157:659–72.
Article
CAS
PubMed
PubMed Central
Google Scholar
Brenner WG, Ramireddy E, Heyl A, Schmülling T. Gene regulation by cytokinin in Arabidopsis. Front Plant Sci. 2012;3:8.
Article
CAS
PubMed
PubMed Central
Google Scholar
Xiong Y, Liu T, Tian C, Sun S, Li J, Chen M. Transcription factors in rice: A genome-wide comparative analysis between monocots and eudicots. Plant Mol Biol. 2005;59:191–203.
Article
CAS
PubMed
Google Scholar
Smalle J, Kurepa J, Yang P, Babiychuk E, Kushnir S, Durski A, Vierstra RD. Cytokinin growth responses in Arabidopsis involve the 26S proteasome subunit RPN12. Plant Cell. 2002;14:17–32.
Article
CAS
PubMed
PubMed Central
Google Scholar
Li Y, Kurepa J, Smalle J. AXR1 promotes the Arabidopsis cytokinin response by facilitating ARR5 proteolysis. Plant J. 2013;74:13–24.
Article
CAS
PubMed
Google Scholar
Kurepa J, Li Y, Smalle JA. Cytokinin signaling stabilizes the response activator ARR1. Plant J. 2014;78:157–68.
Article
CAS
PubMed
Google Scholar
Kim HJ, Chiang Y-H, Kieber JJ, Schaller GE. SCF(KMD) controls cytokinin signaling by regulating the degradation of type-B response regulators. Proc Natl Acad Sci U S A. 2013;110:10028–33.
Article
CAS
PubMed
PubMed Central
Google Scholar
Kim K, Ryu H, Cho YH, Scacchi E, Sabatini S, Hwang I. Cytokinin-facilitated proteolysis of ARABIDOPSIS RESPONSE REGULATOR 2 attenuates signaling output in two-component circuitry. Plant J. 2012;69:934–45.
Article
CAS
PubMed
Google Scholar
Vogel JP, Woeste KW, Theologis A, Kieber JJ. Recessive and dominant mutations in the ethylene biosynthetic gene ACS5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively. Proc Natl Acad Sci U S A. 1998;95:4766–71.
Article
CAS
PubMed
PubMed Central
Google Scholar
Chae HS, Faure F, Kieber JJ. The eto1, eto2 and eto3 mutations and cytokinin treatment elevate ethylene biosynthesis in Arabidopsis by increasing the stability of the ACS5 protein. Plant Cell. 2003;15:545–59.
Article
CAS
PubMed
PubMed Central
Google Scholar
Marhavý P, Duclercq J, Weller B, Feraru E, Bielach A, Offringa R, Friml J, Schwechheimer C, Murphy A, Benková E. Cytokinin controls polarity of PIN1-dependent auxin transport during lateral root organogenesis. Curr Biol. 2014;24:1031–7.
Article
PubMed
Google Scholar
Takagi S, Nomoto K, Takemoto T. Physiological aspect of mugineic acid, a possible phytosiderophore of graminaceous plants. J Plant Nutr. 1984;7:469–77.
Article
CAS
Google Scholar
Römheld V, Marschner H. Evidence for a specific uptake system for iron phytosiderophores in roots of grasses. Plant Physiol. 1986;80:175–80.
Article
PubMed
PubMed Central
Google Scholar
Nozoye T, Nagasaka S, Kobayashi T, Takahashi M, Sato Y, Sato Y, Uozumi N, Nakanishi H, Nishizawa NK. Phytosiderophore efflux transporters are crucial for iron acquisition in graminaceous plants. J Biol Chem. 2011;286:5446–54.
Article
CAS
PubMed
Google Scholar
Ptashnyk M, Roose T, Jones DL, Kirk GJD. Enhanced zinc uptake by rice through phytosiderophore secretion: a modelling study. Plant Cell Environ. 2011;34:2038–46.
Article
CAS
PubMed
Google Scholar
Thimm O, Bläsing O, Gibon Y, Nagel A, Meyer S, Krüger P, Selbig J, Müller LA, Rhee SY, Stitt M. MAPMAN: a user-driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes. Plant J. 2004;37:914–39.
Article
CAS
PubMed
Google Scholar
Shimono M, Sugano S, Nakayama A, Jiang CJ, Ono K, Toki S, Takatsuji H. Rice WRKY45 plays a crucial role in benzothiadiazole-inducible blast resistance. Plant Cell. 2007;19:2064–76.
Article
CAS
PubMed
PubMed Central
Google Scholar
Zhou Y-L, Xu M-R, Zhao M-F, Xie X-W, Zhu L-H, Fu B-Y, Li Z-K. Genome-wide gene responses in a transgenic rice line carrying the maize resistance gene Rxo1 to the rice bacterial streak pathogen, Xanthomonas oryzae pv. oryzicola. BMC Genomics. 2010;11:78.
Article
PubMed
PubMed Central
Google Scholar
Wei T, Ou B, Li J, Zhao Y, Guo D, Zhu Y, Chen Z, Gu H, Li C, Qin G, et al. Transcriptional profiling of rice early response to Magnaporthe oryzae identified OsWRKYs as important regulators in rice blast resistance. PLoS One. 2013;8:e59720.
Article
CAS
PubMed
PubMed Central
Google Scholar
Jiang C-J, Shimono M, Sugano S, Kojima M, Liu X, Inoue H, Sakakibara H, Takatsuji H. Cytokinins act synergistically with salicylic acid to activate defense gene expression in rice. Mol Plant Microbe Interact. 2012;26:287–96.
Article
Google Scholar
Argueso CT, Ferreira FJ, Hutchison CE, To JPC, Epple P, Mathews DE, Schaller GE, Dangl JL, Kieber JJ. Two-component elements mediate interactions between cytokinin and salicylic acid in plant immunity. PLoS Genet. 2012;8:e1002448.
Article
CAS
PubMed
PubMed Central
Google Scholar
McHale L, Tan X, Koehl P, Michelmore RW. Plant NBS-LRR proteins: adaptable guards. Genome Biol. 2006;7:212.
Article
PubMed
PubMed Central
Google Scholar
Shiu SH, Karlowski WM, Pan R, Tzeng YH, Mayer KF, Li WH. Comparative analysis of the receptor-like kinase family in Arabidopsis and rice. Plant Cell. 2004;16:1220–34.
Article
CAS
PubMed
PubMed Central
Google Scholar
Ryu H-S, Han M, Lee S-K, Cho J-I, Ryoo N, Heu S, Lee Y-H, Bhoo S, Wang G-L, Hahn T-R, et al. A comprehensive expression analysis of the WRKY gene superfamily in rice plants during defense response. Plant Cell Rep. 2006;25:836–47.
Article
CAS
PubMed
Google Scholar
Eulgem T, Somssich IE. Networks of WRKY transcription factors in defense signaling. Curr Opin Plant Biol. 2007;10:366–71.
Article
CAS
PubMed
Google Scholar
Ross CA, Liu Y, Shen QJ. The WRKY gene family in rice (Oryza sativa). J Integr Plant Biol. 2007;49:827–42.
Article
CAS
Google Scholar
Cheng H, Liu H, Deng Y, Xiao J, Li X, Wang S. The WRKY45-2 WRKY13 WRKY42 transcriptional regulatory cascade is required for rice resistance to fungal pathogen. Plant Physiol. 2015;167:1087–99.
Article
CAS
PubMed
PubMed Central
Google Scholar
Chujo T, Takai R, Akimoto-Tomiyama C, Ando S, Minami E, Nagamura Y, Kaku H, Shibuya N, Yasuda M, Nakashita H, et al. Involvement of the elicitor-induced gene OsWRKY53 in the expression of defense-related genes in rice. Biochim Biophys Acta. 2007;1769:497–505.
Article
CAS
PubMed
Google Scholar
Liu X, Bai X, Wang X, Chu C. OsWRKY71, a rice transcription factor, is involved in rice defense response. J Plant Physiol. 2007;164:969–79.
Article
CAS
PubMed
Google Scholar
Peng Y, Bartley LE, Canlas P, Ronald PC. OsWRKY IIa transcription factors modulate rice innate immunity. Rice. 2010;3:36–42.
Article
PubMed
PubMed Central
Google Scholar
Shimono M, Koga H, Akagi AYA, Hayashi N, Goto S, Sawada M, Kurihara T, Matsushita A, Sugano S, Jiang C-J, et al. Rice WRKY45 plays important roles in fungal and bacterial disease resistance. Mol Plant Pathol. 2012;13:83–94.
Article
CAS
PubMed
Google Scholar
Nakayama A, Fukushima S, Goto S, Matsushita A, Shimono M, Sugano S, Jiang C-J, Akagi A, Yamazaki M, Inoue H, et al. Genome-wide identification of WRKY45-regulated genes that mediate benzothiadiazole-induced defense responses in rice. BMC Plant Biol. 2013;13:150.
Article
PubMed
PubMed Central
Google Scholar
Akagi A, Fukushima S, Okada K, Jiang C-J, Yoshida R, Nakayama A, Shimono M, Sugano S, Yamane H, Takatsuji H. WRKY45-dependent priming of diterpenoid phytoalexin biosynthesis in rice and the role of cytokinin in triggering the reaction. Plant Mol Biol. 2014;86:171–83.
Article
CAS
PubMed
PubMed Central
Google Scholar
Ma JF, Goto S, Tamai K, Ichii M. Role of root hairs and lateral roots in silicon uptake by rice. Plant Physiol. 2001;127:1773–80.
Article
CAS
PubMed
PubMed Central
Google Scholar
Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10:R25.
Article
PubMed
PubMed Central
Google Scholar