Transcriptional control of hydrogen peroxide homeostasis regulates ground tissue patterning in the Arabidopsis root
暂无分享,去创建一个
Soo-Hwan Kim | J. Choi | Jun Lim | E. K. Yoon | Jung-ok Heo | Sejeong Jang | J. Oh | Seung Woo Kim | Seung Woo Kim | Soo-Hwan Kim | Soo-Hwan Kim
[1] Junxia Wang,et al. NAC1 regulates root ground tissue maturation through coordinating with SCR/SHR-CYCD6;1 module in Arabidopsis. , 2023, Molecular plant.
[2] M. Del Bianco,et al. It’s Time for a Change: The Role of Gibberellin in Root Meristem Development , 2022, Frontiers in Plant Science.
[3] Jun Lim,et al. SHORT-ROOT Controls Cell Elongation in the Etiolated Arabidopsis Hypocotyl , 2022, Molecules and cells.
[4] Marcela Hernández-Coronado,et al. Root Patterning: Tuning SHORT ROOT Function Creates Diversity in Form , 2021, Frontiers in Plant Science.
[5] Hironaka Tsukagoshi,et al. Reactive Oxygen Species Link Gene Regulatory Networks During Arabidopsis Root Development , 2021, Frontiers in Plant Science.
[6] Takeshi Ito,et al. SCARECROW-LIKE3 regulates the transcription of gibberellin-related genes by acting as a transcriptional co-repressor of GAI-ASSOCIATED FACTOR1 , 2021, Plant Molecular Biology.
[7] Riccardo Di Mambro,et al. A PHABULOSA-Controlled Genetic Pathway Regulates Ground Tissue Patterning in the Arabidopsis Root , 2020, Current Biology.
[8] Guanghui Yu,et al. Modulatory Role of Reactive Oxygen Species in Root Development in Model Plant of Arabidopsis thaliana , 2020, Frontiers in Plant Science.
[9] Shuang Wu,et al. Hydrogen peroxide homeostasis provides beneficial micro-environment for SHR-mediated periclinal division in Arabidopsis root. , 2020, The New phytologist.
[10] Yuguo Zheng,et al. Integrated bioinformatics analyses identified SCL3-induced regulatory network in Arabidopsis thaliana roots , 2020, Biotechnology Letters.
[11] Giovanna Di Ruocco,et al. Building the differences: a case for the ground tissue patterning in plants , 2018, Proceedings of the Royal Society B.
[12] Shuang Wu,et al. Cell-Fate Specification in Arabidopsis Roots Requires Coordinative Action of Lineage Instruction and Positional Reprogramming1[OPEN] , 2017, Plant Physiology.
[13] J. Choi,et al. Conservation and Diversification of the SHR-SCR-SCL23 Regulatory Network in the Development of the Functional Endodermis in Arabidopsis Shoots. , 2016, Molecular plant.
[14] J. Choi,et al. Control of Asymmetric Cell Divisions during Root Ground Tissue Maturation , 2016, Molecules and cells.
[15] Hongchang Cui. Middle Cortex Formation in the Root: An Emerging Picture of Integrated Regulatory Mechanisms. , 2016, Molecular plant.
[16] J. Choi,et al. Interplay between ABA and GA Modulates the Timing of Asymmetric Cell Divisions in the Arabidopsis Root Ground Tissue. , 2016, Molecular plant.
[17] Prakash P. Kumar,et al. Plant hormone-mediated regulation of stress responses , 2016, BMC Plant Biology.
[18] Eunkyoo Oh,et al. Information Integration and Communication in Plant Growth Regulation , 2016, Cell.
[19] Y. Tsutsumi,et al. Diverse functions and reactions of class III peroxidases. , 2016, The New phytologist.
[20] Hironaka Tsukagoshi. Control of root growth and development by reactive oxygen species. , 2016, Current opinion in plant biology.
[21] Zhongchi Liu,et al. SEUSS Integrates Gibberellin Signaling with Transcriptional Inputs from the SHR-SCR-SCL3 Module to Regulate Middle Cortex Formation in the Arabidopsis Root1[OPEN] , 2016, Plant Physiology.
[22] Khader Shameer,et al. Transcriptional regulatory networks in Arabidopsis thaliana during single and combined stresses , 2015, Nucleic acids research.
[23] Uwe Ohler,et al. Transcriptional control of tissue formation throughout root development , 2015, Science.
[24] Hongchang Cui. Cortex proliferation in the root is a protective mechanism against abiotic stress , 2015, Plant signaling & behavior.
[25] C. Foyer,et al. Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance. , 2015, Journal of experimental botany.
[26] C. Dunand,et al. Roles of cell wall peroxidases in plant development. , 2015, Phytochemistry.
[27] J. Li,et al. SPINDLY, ERECTA, and Its Ligand STOMAGEN Have a Role in Redox-Mediated Cortex Proliferation in the Arabidopsis Root , 2014, Molecular plant.
[28] Shuang Wu,et al. A plausible mechanism, based upon SHORT-ROOT movement, for regulating the number of cortex cell layers in roots , 2014, Proceedings of the National Academy of Sciences.
[29] H. Yoshida,et al. DELLA and SCL3 balance gibberellin feedback regulation by utilizing INDETERMINATE DOMAIN proteins as transcriptional scaffolds , 2014, Plant signaling & behavior.
[30] P. Dhonukshe,et al. Formative cell divisions: principal determinants of plant morphogenesis. , 2013, Plant & cell physiology.
[31] K. Gallagher,et al. SCARECROW reinforces SHORT-ROOT signaling and inhibits periclinal cell divisions in the ground tissue by maintaining SHR at high levels in the endodermis , 2012, Plant signaling & behavior.
[32] James A.H. Murray,et al. A Bistable Circuit Involving SCARECROW-RETINOBLASTOMA Integrates Cues to Inform Asymmetric Stem Cell Division , 2012, Cell.
[33] Shuang Wu,et al. The SHORT-ROOT protein acts as a mobile, dose-dependent signal in patterning the ground tissue , 2012, Proceedings of the National Academy of Sciences.
[34] B. Galatis,et al. Plant cell division , 2012, Plant signaling & behavior.
[35] Kevin W Eliceiri,et al. NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.
[36] Philip N Benfey,et al. Control of Arabidopsis root development. , 2012, Annual review of plant biology.
[37] F. Divol,et al. Surfing along the root ground tissue gene network. , 2012, Developmental biology.
[38] F. Ausubel,et al. A Peroxidase-Dependent Apoplastic Oxidative Burst in Cultured Arabidopsis Cells Functions in MAMP-Elicited Defense1[W][OA] , 2012, Plant Physiology.
[39] F. Ausubel,et al. The Apoplastic Oxidative Burst Peroxidase in Arabidopsis Is a Major Component of Pattern-Triggered Immunity[W][OA] , 2012, Plant Cell.
[40] T. Beeckman,et al. Asymmetric cell division in land plants and algae: the driving force for differentiation , 2011, Nature Reviews Molecular Cell Biology.
[41] Yuji Kamiya,et al. SCARECROW-LIKE 3 promotes gibberellin signaling by antagonizing master growth repressor DELLA in Arabidopsis , 2011, Proceedings of the National Academy of Sciences.
[42] Sang-Kee Song,et al. Funneling of gibberellin signaling by the GRAS transcription regulator SCARECROW-LIKE 3 in the Arabidopsis root , 2011, Proceedings of the National Academy of Sciences.
[43] P. Benfey,et al. Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root , 2010, Cell.
[44] Dong Xu,et al. Identification of transcription factor's targets using tissue-specific transcriptomic data in Arabidopsis thaliana , 2010, BMC Systems Biology.
[45] P. Benfey,et al. Spatiotemporal regulation of cell-cycle genes by SHORTROOT links patterning and growth , 2010, Nature.
[46] D. Bergmann,et al. Asymmetric cell divisions: a view from plant development. , 2009, Developmental cell.
[47] P. Benfey,et al. Cortex proliferation , 2009 .
[48] G. Jürgens,et al. Survival of the flexible: hormonal growth control and adaptation in plant development , 2009, Nature Reviews Genetics.
[49] C. Dunand,et al. Specific functions of individual class III peroxidase genes. , 2009, Journal of experimental botany.
[50] J. Knoblich,et al. Mechanisms of Asymmetric Stem Cell Division , 2008, Cell.
[51] R. Heidstra,et al. Who begets whom? Plant cell fate determination by asymmetric cell division. , 2008, Current opinion in plant biology.
[52] Yuji Kamiya,et al. Global Analysis of DELLA Direct Targets in Early Gibberellin Signaling in Arabidopsis[W] , 2007, The Plant Cell Online.
[53] Teva Vernoux,et al. An Evolutionarily Conserved Mechanism Delimiting SHR Movement Defines a Single Layer of Endodermis in Plants , 2007, Science.
[54] C. Dunand,et al. Distribution of superoxide and hydrogen peroxide in Arabidopsis root and their influence on root development: possible interaction with peroxidases. , 2007, The New phytologist.
[55] D. Davies,et al. Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance. , 2006, The Plant journal : for cell and molecular biology.
[56] L. Dolan,et al. Control of Plant Development by Reactive Oxygen Species1 , 2006, Plant Physiology.
[57] C. Dunand,et al. Two cell wall associated peroxidases from Arabidopsis influence root elongation , 2006, Planta.
[58] Patrick Achard,et al. Integration of Plant Responses to Environmentally Activated Phytohormonal Signals , 2006, Science.
[59] P. Benfey,et al. Maturation of the Ground Tissue of the Root Is Regulated by Gibberellin and SCARECROW and Requires SHORT-ROOT1[w] , 2005, Plant Physiology.
[60] R. Mittler,et al. Reactive oxygen gene network of plants. , 2004, Trends in plant science.
[61] B. Scheres,et al. Mosaic analyses using marked activation and deletion clones dissect Arabidopsis SCARECROW action in asymmetric cell division. , 2004, Genes & development.
[62] C. Dunand,et al. Expression analysis of the Arabidopsis peroxidase multigenic family. , 2004, Phytochemistry.
[63] H. Hirt,et al. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. , 2004, Annual review of plant biology.
[64] T. Sun,et al. Molecular mechanism of gibberellin signaling in plants. , 2004, Annual review of plant biology.
[65] J. G. Dubrovsky,et al. Apical organization and maturation of the cortex and vascular cylinder inArabidopsis thaliana (Brassicaceae) roots. , 2002, American journal of botany.
[66] M. Tognolli,et al. Analysis and expression of the class III peroxidase large gene family in Arabidopsis thaliana. , 2002, Gene.
[67] T. Sun,et al. Synergistic derepression of gibberellin signaling by removing RGA and GAI function in Arabidopsis thaliana. , 2001, Genetics.
[68] C. Foyer,et al. Early H(2)O(2) accumulation in mesophyll cells leads to induction of glutathione during the hyper-sensitive response in the barley-powdery mildew interaction. , 2000, Plant physiology.
[69] Philip N Benfey,et al. The SHORT-ROOT Gene Controls Radial Patterning of the Arabidopsis Root through Radial Signaling , 2000, Cell.
[70] T. Sun,et al. The Arabidopsis RGA Gene Encodes a Transcriptional Regulator Repressing the Gibberellin Signal Transduction Pathway , 1998, Plant Cell.
[71] David B. Collinge,et al. Subcellular localization of H2O2 in plants. H2O2 accumulation in papillae and hypersensitive response during the barley—powdery mildew interaction , 1997 .
[72] T. Sun,et al. The new RGA locus encodes a negative regulator of gibberellin response in Arabidopsis thaliana. , 1997, Genetics.
[73] S. Jacobsen,et al. SPINDLY, a tetratricopeptide repeat protein involved in gibberellin signal transduction in Arabidopsis. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[74] P. Benfey,et al. The SCARECROW Gene Regulates an Asymmetric Cell Division That Is Essential for Generating the Radial Organization of the Arabidopsis Root , 1996, Cell.
[75] T. Sun,et al. The Arabidopsis GA1 locus encodes the cyclase ent-kaurene synthetase A of gibberellin biosynthesis. , 1994, The Plant cell.
[76] C. Dean,et al. Embryonic origin of the Arabidopsis primary root and root meristem initials , 1994 .
[77] P. Benfey,et al. Root development in Arabidopsis: four mutants with dramatically altered root morphogenesis. , 1993, Development.
[78] B. Scheres,et al. Cellular organisation of the Arabidopsis thaliana root. , 1993, Development.
[79] S. Jacobsen,et al. Mutations at the SPINDLY locus of Arabidopsis alter gibberellin signal transduction. , 1993, The Plant cell.
[80] Ira Herskowitz,et al. Mechanisms of asymmetric cell division: Two Bs or not two Bs, that is the question , 1992, Cell.
[81] Jing Jiang,et al. MPK6 controls H2 O2-induced root elongation by mediating Ca2+ influx across the plasma membrane of root cells in Arabidopsis seedlings. , 2015, The New phytologist.
[82] P. Benfey,et al. Cortex proliferation: simple phenotype, complex regulatory mechanisms. , 2009, Plant signaling & behavior.
[83] P. Benfey,et al. Mutations affecting the radial organisation of the Arabidopsis root display specific defects throughout the embryonic axis , 1995 .