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1.
Front Plant Sci ; 15: 1369299, 2024.
Article in English | MEDLINE | ID: mdl-38681221

ABSTRACT

The Flavin Monooxygenase (FMO) gene superfamily in plants is involved in various processes most widely documented for its involvement in auxin biosynthesis, specialized metabolite biosynthesis, and plant microbial defense signaling. The roles of FMOs in defense signaling and disease resistance have recently come into focus as they may present opportunities to increase immune responses in plants including leading to systemic acquired resistance, but are not well characterized. We present a comprehensive catalogue of FMOs found in genomes across vascular plants and explore, in depth, 170 wheat TaFMO genes for sequence architecture, cis-acting regulatory elements, and changes due to Transposable Element insertions. A molecular phylogeny separates TaFMOs into three clades (A, B, and C) for which we further report gene duplication patterns, and differential rates of homoeologue expansion and retention among TaFMO subclades. We discuss Clade B TaFMOs where gene expansion is similarly seen in other cereal genomes. Transcriptome data from various studies point towards involvement of subclade B2 TaFMOs in disease responses against both biotrophic and necrotrophic pathogens, substantiated by promoter element analysis. We hypothesize that certain TaFMOs are responsive to both abiotic and biotic stresses, providing potential targets for enhancing disease resistance, plant yield and other important agronomic traits. Altogether, FMOs in wheat and other crop plants present an untapped resource to be exploited for improving the quality of crops.

2.
Science ; 376(6598): 1187-1191, 2022 06 10.
Article in English | MEDLINE | ID: mdl-35679407

ABSTRACT

Many plant-associated fungi are obligate biotrophs that depend on living hosts to proliferate. However, little is known about the molecular basis of the biotrophic lifestyle, despite the impact of fungi on the environment and food security. In this work, we show that combinations of organic acids and glucose trigger phenotypes that are associated with the late stage of biotrophy for the maize pathogen Ustilago maydis. These phenotypes include the expression of a set of effectors normally observed only during biotrophic development, as well as the formation of melanin associated with sporulation in plant tumors. U. maydis and other hemibiotrophic fungi also respond to a combination of carbon sources with enhanced proliferation. Thus, the response to combinations of nutrients from the host may be a conserved feature of fungal biotrophy.


Subject(s)
Dicarboxylic Acids , Glucose , Host-Pathogen Interactions , Plant Tumors , Ustilago , Zea mays , Dicarboxylic Acids/metabolism , Fungal Proteins/genetics , Fungal Proteins/metabolism , Glucose/metabolism , Plant Tumors/microbiology , Ustilago/genetics , Ustilago/metabolism , Ustilago/pathogenicity , Virulence , Zea mays/microbiology
3.
J Biol Chem ; 278(40): 38821-8, 2003 Oct 03.
Article in English | MEDLINE | ID: mdl-12819202

ABSTRACT

The structures of the liver X receptor LXRbeta (NR1H2) have been determined in complexes with two synthetic ligands, T0901317 and GW3965, to 2.1 and 2.4 A, respectively. Together with its isoform LXRalpha (NR1H3) it regulates target genes involved in metabolism and transport of cholesterol and fatty acids. The two LXRbeta structures reveal a flexible ligand-binding pocket that can adjust to accommodate fundamentally different ligands. The ligand-binding pocket is hydrophobic but with polar or charged residues at the two ends of the cavity. T0901317 takes advantage of this by binding to His-435 close to H12 while GW3965 orients itself with its charged group in the opposite direction. Both ligands induce a fixed "agonist conformation" of helix H12 (also called the AF-2 domain), resulting in a transcriptionally active receptor.


Subject(s)
Receptors, Cytoplasmic and Nuclear/chemistry , Alanine/chemistry , Binding Sites , Cholesterol/metabolism , DNA-Binding Proteins , Dimerization , Electrons , Escherichia coli/metabolism , Histidine/chemistry , Humans , Ligands , Liver X Receptors , Models, Chemical , Models, Molecular , Models, Statistical , Orphan Nuclear Receptors , Protein Binding , Protein Conformation , Protein Isoforms , Protein Structure, Tertiary , Receptors, Cytoplasmic and Nuclear/metabolism , Transcription Factors/metabolism , Transcription, Genetic , X-Rays
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