The fungal NADPH oxidase is an essential element for the molecular dialogue between Trichoderma and Arabidopsis.
暂无分享,去创建一个
A. Herrera-Estrella | J. M. Villalobos-Escobedo | Ramón Pelagio-Flores | J. López‐Bucio | Saraí Esparza-Reynoso | A. Herrera‐Estrella | L. F. Ruíz-Herrera | Fabiola López-Ramírez
[1] J. Poveda,et al. The Trichoderma harzianum Kelch Protein ThKEL1 Plays a Key Role in Root Colonization and the Induction of Systemic Defense in Brassicaceae Plants , 2019, Front. Plant Sci..
[2] V. Olmedo-Monfil,et al. Trichoderma as a Model to Study Effector-Like Molecules , 2019, Front. Microbiol..
[3] C. Kenerley,et al. Differential expression analysis of Trichoderma virens RNA reveals a dynamic transcriptome during colonization of Zea mays roots , 2019, BMC Genomics.
[4] M. Nieto-Jacobo,et al. The NADPH Oxidases Nox1 and Nox2 Differentially Regulate Volatile Organic Compounds, Fungistatic Activity, Plant Growth Promotion and Nutrient Assimilation in Trichoderma atroviride , 2019, Front. Microbiol..
[5] K. Saravanakumar,et al. Yeast two-hybrid and label-free proteomics based screening of maize root receptor to cellulase of Trichoderma harzianum , 2018, Physiological and Molecular Plant Pathology.
[6] C. Abreu-Goodger,et al. Danger signals activate a putative innate immune system during regeneration in a filamentous fungus , 2018, PLoS genetics.
[7] G. Howe,et al. JAZ repressors of metabolic defense promote growth and reproductive fitness in Arabidopsis , 2018, Proceedings of the National Academy of Sciences.
[8] T. Tschaplinski,et al. Regulation of Lignin Biosynthesis and Its Role in Growth-Defense Tradeoffs , 2018, Front. Plant Sci..
[9] L. Macías-Rodríguez,et al. Trichoderma atroviride promotes tomato development and alters the root exudation of carbohydrates, which stimulates fungal growth and the biocontrol of the phytopathogen Phytophthora cinnamomi in a tripartite interaction system. , 2018, FEMS microbiology ecology.
[10] B. Horwitz,et al. Molecular dialogues between Trichoderma and roots: Role of the fungal secretome , 2018 .
[11] A. Tanaka,et al. Two closely related Rho GTPases, Cdc42 and RacA, of the en-dophytic fungus Epichloë festucae have contrasting roles for ROS production and symbiotic infection synchronized with the host plant , 2018, PLoS pathogens.
[12] D. Zafari,et al. Volatile organic compounds of some Trichoderma spp. increase growth and induce salt tolerance in Arabidopsis thaliana , 2017 .
[13] A. Herrera-Estrella,et al. Trichoderma-Induced Acidification Is an Early Trigger for Changes in Arabidopsis Root Growth and Determines Fungal Phytostimulation , 2017, Front. Plant Sci..
[14] Geet Duggal,et al. Salmon: fast and bias-aware quantification of transcript expression using dual-phase inference , 2017, Nature Methods.
[15] Huang Huang,et al. Jasmonate action in plant growth and development , 2017, Journal of experimental botany.
[16] S. Molinari,et al. Induction of SA-signaling pathway and ethylene biosynthesis in Trichoderma harzianum-treated tomato plants after infection of the root-knot nematode Meloidogyne incognita , 2017, Plant Cell Reports.
[17] A. Herrera-Estrella,et al. Identification of effector-like proteins in Trichoderma spp. and role of a hydrophobin in the plant-fungus interaction and mycoparasitism , 2017, BMC Genetics.
[18] M. Nieto-Jacobo,et al. Environmental Growth Conditions of Trichoderma spp. Affects Indole Acetic Acid Derivatives, Volatile Organic Compounds, and Plant Growth Promotion , 2017, Front. Plant Sci..
[19] P. Castillo,et al. Tomato progeny inherit resistance to the nematode Meloidogyne javanica linked to plant growth induced by the biocontrol fungus Trichoderma atroviride , 2017, Scientific Reports.
[20] M. Wang,et al. Cellulase from Trichoderma harzianum interacts with roots and triggers induced systemic resistance to foliar disease in maize , 2016, Scientific Reports.
[21] X. Draye,et al. RBOH-mediated ROS production facilitates lateral root emergence in Arabidopsis , 2016, Development.
[22] L. Ruíz-Herrera,et al. Serotonin modulates Arabidopsis root growth via changes in reactive oxygen species and jasmonic acid-ethylene signaling. , 2016, Physiologia plantarum.
[23] Philipp C. Münch,et al. Survival trade-offs in plant roots during colonization by closely related beneficial and pathogenic fungi , 2016, Nature Communications.
[24] B. Scott,et al. The endophytic symbiont Epichloë festucae establishes an epiphyllous net on the surface of Lolium perenne leaves by development of an expressorium, an appressorium‐like leaf exit structure , 2016, The New phytologist.
[25] L. Macías-Rodríguez,et al. The volatile 6-pentyl-2H-pyran-2-one from Trichoderma atroviride regulates Arabidopsis thaliana root morphogenesis via auxin signaling and ETHYLENE INSENSITIVE 2 functioning. , 2016, The New phytologist.
[26] D. M. Roberts,et al. Arabidopsis CML38, a Calcium Sensor That Localizes to Ribonucleoprotein Complexes under Hypoxia Stress1[OPEN] , 2015, Plant Physiology.
[27] A. Herrera-Estrella,et al. Trichoderma as biostimulant: exploiting the multilevel properties of a plant beneficial fungus , 2015 .
[28] Dominik K. Grosskinsky,et al. Trichoderma volatiles effecting Arabidopsis: from inhibition to protection against phytopathogenic fungi , 2015, Front. Microbiol..
[29] D. Kliebenstein,et al. Transcriptional networks governing plant metabolism , 2015 .
[30] L. Macías-Rodríguez,et al. Mitogen-Activated Protein Kinase 6 and Ethylene and Auxin Signaling Pathways Are Involved in Arabidopsis Root-System Architecture Alterations by Trichoderma atroviride. , 2015, Molecular plant-microbe interactions : MPMI.
[31] C. Xiang,et al. Arabidopsis ERF109 mediates cross-talk between jasmonic acid and auxin biosynthesis during lateral root formation , 2014, Nature Communications.
[32] Simon R. Law,et al. The mitochondrial outer membrane AAA ATPase AtOM66 affects cell death and pathogen resistance in Arabidopsis thaliana. , 2014, The Plant journal : for cell and molecular biology.
[33] S. He,et al. Growth-defense tradeoffs in plants: a balancing act to optimize fitness. , 2014, Molecular plant.
[34] L. Macías-Rodríguez,et al. Trichoderma spp. Improve growth of Arabidopsis seedlings under salt stress through enhanced root development, osmolite production, and Na⁺ elimination through root exudates. , 2014, Molecular plant-microbe interactions : MPMI.
[35] A. Herrera-Estrella,et al. The 4-phosphopantetheinyl transferase of Trichoderma virens plays a role in plant protection against Botrytis cinerea through volatile organic compound emission , 2014, Plant and Soil.
[36] N. M. Quijada,et al. Identifying Beneficial Qualities of Trichoderma parareesei for Plants , 2014, Applied and Environmental Microbiology.
[37] Hsien-Da Huang,et al. Fungal Small RNAs Suppress Plant Immunity by Hijacking Host RNA Interference Pathways , 2013, Science.
[38] J. Kangasjärvi,et al. ROS signaling loops - production, perception, regulation. , 2013, Current opinion in plant biology.
[39] C. Abreu-Goodger,et al. The RNAi machinery regulates growth and development in the filamentous fungus Trichoderma atroviride , 2013, Molecular microbiology.
[40] C. Wasternack,et al. Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. , 2013, Annals of botany.
[41] Yunde Zhao,et al. The jasmonic acid signaling pathway is linked to auxin homeostasis through the modulation of YUCCA8 and YUCCA9 gene expression. , 2013, The Plant journal : for cell and molecular biology.
[42] S. Gutiérrez,et al. The contribution of Trichoderma to balancing the costs of plant growth and defense. , 2013, International microbiology : the official journal of the Spanish Society for Microbiology.
[43] A. Fernie,et al. Trichoderma-Plant Root Colonization: Escaping Early Plant Defense Responses and Activation of the Antioxidant Machinery for Saline Stress Tolerance , 2013, PLoS pathogens.
[44] E. Esquivel-Naranjo,et al. An injury-response mechanism conserved across kingdoms determines entry of the fungus Trichoderma atroviride into development , 2012, Proceedings of the National Academy of Sciences.
[45] S. Zeilinger,et al. The seven-transmembrane receptor Gpr1 governs processes relevant for the antagonistic interaction of Trichoderma atroviride with its host , 2012, Microbiology.
[46] A. Hernández-Morales,et al. Role of the 4-phosphopantetheinyl transferase of Trichoderma virens in secondary metabolism and induction of plant defense responses. , 2011, Molecular plant-microbe interactions : MPMI.
[47] A. Herrera-Estrella,et al. Trichoderma-induced plant immunity likely involves both hormonal- and camalexin-dependent mechanisms in Arabidopsis thaliana and confers resistance against necrotrophic fungi Botrytis cinerea. , 2011, Plant signaling & behavior.
[48] Gary J Loake,et al. Transcription Dynamics in Plant Immunity , 2011, Plant Cell.
[49] K. Palme,et al. Jasmonate modulates endocytosis and plasma membrane accumulation of the Arabidopsis PIN2 protein. , 2011, The New phytologist.
[50] Mariana Rivas-San Vicente,et al. Salicylic acid beyond defence: its role in plant growth and development. , 2011, Journal of experimental botany.
[51] S. Gutiérrez,et al. Functional Analysis of the Trichoderma harzianum nox1 Gene, Encoding an NADPH Oxidase, Relates Production of Reactive Oxygen Species to Specific Biocontrol Activity against Pythium ultimum , 2011, Applied and Environmental Microbiology.
[52] S. Shigeoka,et al. Understanding Oxidative Stress and Antioxidant Functions to Enhance Photosynthesis1 , 2010, Plant Physiology.
[53] S. Campbell,et al. Direct Activation of RhoA by Reactive Oxygen Species Requires a Redox-Sensitive Motif , 2009, PloS one.
[54] D. Archer,et al. SOD1-targeted gene disruption in the ericoid mycorrhizal fungus Oidiodendron maius reduces conidiation and the capacity for mycorrhization. , 2009, Molecular plant-microbe interactions : MPMI.
[55] John Mandawe,et al. Plant-Derived Sucrose Is a Key Element in the Symbiotic Association between Trichoderma virens and Maize Plants1[C][W] , 2009, Plant Physiology.
[56] D. Inzé,et al. Expression of the Arabidopsis jasmonate signalling repressor JAZ1/TIFY10A is stimulated by auxin , 2009, EMBO reports.
[57] K. Palme,et al. Arabidopsis ASA1 Is Important for Jasmonate-Mediated Regulation of Auxin Biosynthesis and Transport during Lateral Root Formation[W][OA] , 2009, The Plant Cell Online.
[58] L. Macías-Rodríguez,et al. Trichoderma virens, a Plant Beneficial Fungus, Enhances Biomass Production and Promotes Lateral Root Growth through an Auxin-Dependent Mechanism in Arabidopsis1[C][W][OA] , 2009, Plant Physiology.
[59] B. Ezaki,et al. Functions of two genes in aluminium (Al) stress resistance: repression of oxidative damage by the AtBCB gene and promotion of efflux of Al ions by the NtGDI1gene. , 2005, Journal of experimental botany.
[60] S. Meloche,et al. Rho Family GTPases Are Required for Activation of Jak/STAT Signaling by G Protein-Coupled Receptors , 2003, Molecular and Cellular Biology.
[61] Hong-Gu Kang,et al. Characterization of salicylic acid-responsive, arabidopsis Dof domain proteins: overexpression of OBP3 leads to growth defects. , 2000, The Plant journal : for cell and molecular biology.
[62] J. Glazebrook,et al. Arabidopsis PAD3, a Gene Required for Camalexin Biosynthesis, Encodes a Putative Cytochrome P450 Monooxygenase , 1999, Plant Cell.
[63] G. Hagen,et al. Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements. , 1997, The Plant cell.
[64] F. Skoog,et al. A revised medium for rapid growth and bio assays with tobacco tissue cultures , 1962 .
[65] Richard A. Wilson,et al. Reactive oxygen species metabolism and plant-fungal interactions. , 2018, Fungal genetics and biology : FG & B.
[66] A. P. Souza,et al. Correction: Author Correction , 2018 .
[67] B. Scott,et al. Morphogenesis, Growth, and Development of the Grass Symbiont Epichlöe festucae , 2012 .
[68] I. Chet,et al. Plant-beneficial effects of Trichoderma and of its genes. , 2012, Microbiology.
[69] Gary E. Harman,et al. Trichoderma species — opportunistic, avirulent plant symbionts , 2004, Nature Reviews Microbiology.
[70] P. Benfey,et al. Organization and cell differentiation in lateral roots of Arabidopsis thaliana. , 1997, Development.