Artificial evolution extends the spectrum of viruses that are targeted by a disease-resistance gene from potato.
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Fine mapping and DNA fiber FISH analysis locates the tobamovirus resistance gene L3 of Capsicum chinense in a 400-kb region of R-like genes cluster embedded in highly repetitive sequences.The cyst nematode SPRYSEC protein RBP-1 elicits Gpa2- and RanGAP2-dependent plant cell deathCo-evolutionary interactions between host resistance and pathogen effector genes in flax rust disease.Intramolecular interaction influences binding of the Flax L5 and L6 resistance proteins to their AvrL567 ligands.Evolution and variability of Solanum RanGAP2, a cofactor in the incompatible interaction between the resistance protein GPA2 and the Globodera pallida effector Gp-RBP-1Elucidation of virus-host interactions to enhance resistance breeding for control of virus diseases in potato.Detection of the virulent form of AVR3a from Phytophthora infestans following artificial evolution of potato resistance gene R3aRecognition and activation domains contribute to allele-specific responses of an Arabidopsis NLR receptor to an oomycete effector proteinMolecular and functional analyses of a maize autoactive NB-LRR protein identify precise structural requirements for activityThe effect on the transcriptome of Anemone coronaria following infection with rust (Tranzschelia discolor).Indirect activation of a plant nucleotide binding site-leucine-rich repeat protein by a bacterial proteaseRandom mutagenesis of the nucleotide-binding domain of NRC1 (NB-LRR Required for Hypersensitive Response-Associated Cell Death-1), a downstream signalling nucleotide-binding, leucine-rich repeat (NB-LRR) protein, identifies gain-of-function mutationDirected Evolution of FLS2 towards Novel Flagellin Peptide Recognition.Leucine zipper motif in RRS1 is crucial for the regulation of Arabidopsis dual resistance protein complex RPS4/RRS1Rumble in the nuclear jungle: compartmentalization, trafficking, and nuclear action of plant immune receptors.From pathogen genomes to host plant processes: the power of plant parasitic oomycetesThe evolution of virulence and pathogenicity in plant pathogen populations.Strategies for antiviral resistance in transgenic plants.Stepwise artificial evolution of a plant disease resistance geneImmune Receptors and Co-receptors in Antiviral Innate Immunity in Plants.Sources of natural resistance to plant viruses: status and prospects.Improving crop disease resistance: lessons from research on Arabidopsis and tomato.Biotechnological strategies and tools for Plum pox virus resistance: trans-, intra-, cis-genesis, and beyondSequence Exchange between Homologous NB-LRR Genes Converts Virus Resistance into Nematode Resistance, and Vice Versa.Plant immunity against viruses: antiviral immune receptors in focus.Fine mapping of RYMV3: a new resistance gene to Rice yellow mottle virus from Oryza glaberrima.Utilization of engineered resistance to viruses in crops of the developing world, with emphasis on sub-Saharan Africa.Evidence for different, host-dependent functioning of Rx against both wild-type and recombinant Pepino mosaic virus.RanGAP2 mediates nucleocytoplasmic partitioning of the NB-LRR immune receptor Rx in the Solanaceae, thereby dictating Rx function.Physical association of the NB-LRR resistance protein Rx with a Ran GTPase-activating protein is required for extreme resistance to Potato virus X.Tsw gene-based resistance is triggered by a functional RNA silencing suppressor protein of the Tomato spotted wilt virus.Rye Pm8 and wheat Pm3 are orthologous genes and show evolutionary conservation of resistance function against powdery mildew.The effector SPRYSEC-19 of Globodera rostochiensis suppresses CC-NB-LRR-mediated disease resistance in plants.Structural determinants at the interface of the ARC2 and leucine-rich repeat domains control the activation of the plant immune receptors Rx1 and Gpa2.Nucleocytoplasmic distribution is required for activation of resistance by the potato NB-LRR receptor Rx1 and is balanced by its functional domains.Cloning of novel rice blast resistance genes from two rapidly evolving NBS-LRR gene families in rice.The coiled-coil and nucleotide binding domains of the Potato Rx disease resistance protein function in pathogen recognition and signaling.Evolutionary and Functional Dynamics of Oomycete Effector GenesEngineering Barriers to Infection by Undermining Pathogen Effector Function or by Gaining Effector Recognition
P2860
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P2860
Artificial evolution extends the spectrum of viruses that are targeted by a disease-resistance gene from potato.
description
2006 nî lūn-bûn
@nan
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Artificial evolution extends t ...... e-resistance gene from potato.
@ast
Artificial evolution extends t ...... e-resistance gene from potato.
@en
Artificial evolution extends t ...... e-resistance gene from potato.
@en-gb
type
label
Artificial evolution extends t ...... e-resistance gene from potato.
@ast
Artificial evolution extends t ...... e-resistance gene from potato.
@en
Artificial evolution extends t ...... e-resistance gene from potato.
@en-gb
prefLabel
Artificial evolution extends t ...... e-resistance gene from potato.
@ast
Artificial evolution extends t ...... e-resistance gene from potato.
@en
Artificial evolution extends t ...... e-resistance gene from potato.
@en-gb
P2860
P356
P1476
Artificial evolution extends t ...... e-resistance gene from potato.
@en
P2093
Garry Farnham
P2860
P304
18828-18833
P356
10.1073/PNAS.0605777103
P407
P577
2006-10-04T00:00:00Z