ABSTRACT
Plants are constantly under attack from a variety of microorganisms, and rely on a series of complex detection and response systems to protect themselves from infection. Here, we found that a by-product of glutamate fermentation triggered defense responses in grapevine, increasing the expression of defense response genes in cultured cells, foliar chitinase activity, and resistance to infection by downy mildew in leaf explants. To identify the molecule that triggered this innate immunity, we fractionated and purified candidates extracted from Corynebacterium glutamicum, a bacterium used in the production of amino acids by fermentation. Using hydrolysis by lysozyme, a silkworm larva plasma detection system, and gel filtration analysis, we identified peptidoglycan as inducing the defense responses. Peptidoglycans of Escherichia coli, Bacillus subtilis, and Staphylococcus aureus also generated similar defensive responses.
Subject(s)
Gene Expression Regulation, Plant/immunology , Peptidoglycan/pharmacology , Plant Diseases/immunology , Plant Leaves/genetics , Plant Proteins/immunology , Vitis/genetics , Bacillus subtilis/metabolism , Chitinases/genetics , Chitinases/immunology , Chitinases/metabolism , Complex Mixtures/chemistry , Corynebacterium glutamicum/metabolism , Escherichia coli/metabolism , Fermentation , Glutamic Acid/metabolism , Peptidoglycan/biosynthesis , Peptidoglycan/isolation & purification , Peronospora/growth & development , Peronospora/pathogenicity , Plant Diseases/genetics , Plant Immunity/drug effects , Plant Immunity/genetics , Plant Leaves/drug effects , Plant Leaves/immunology , Plant Proteins/genetics , Plant Proteins/metabolism , Staphylococcus aureus/metabolism , Vitis/drug effects , Vitis/immunologyABSTRACT
Pollen development is a fundamental and essential biological process in seed plants. Pollen mother cells generated in anthers undergo meiosis, which gives rise to haploid microspores. The haploid cells then develop into mature pollen grains through two mitotic cell divisions. Although several sporophytic and gametophytic mutations affecting male gametogenesis have been identified and analyzed, little is known about the underlying molecular mechanism. In this study, we investigated the function of the TCP16 gene, which encodes a putative transcription factor. Expression analysis of the promoter::GUS fusion gene revealed that TCP16 transcription occurred predominantly in developing microspores. GUS expression began at the tetrad stage and markedly increased in an early unicellular stage. Transgenic plants harboring a TCP16 RNA interference (RNAi) construct generated equal amounts of normal and abnormal pollen grains. The abnormal pollen grains exhibited morphological abnormality and degeneration of genomic DNA. The defective phenotype of the RNAi plants was first detectable at the middle of the unicellular stage. Our results therefore suggest that TCP16, a putative transcription factor, plays a crucial role in early processes in pollen development.
Subject(s)
Arabidopsis Proteins/physiology , Arabidopsis/growth & development , Pollen/growth & development , RNA Interference , Transcription Factors/physiology , Arabidopsis/genetics , Arabidopsis/metabolism , Arabidopsis Proteins/antagonists & inhibitors , Arabidopsis Proteins/genetics , Genes, Plant , Glucuronidase/analysis , Phenotype , Pollen/anatomy & histology , Pollen/genetics , Recombinant Fusion Proteins/analysis , Transcription Factors/antagonists & inhibitors , Transcription Factors/geneticsABSTRACT
cDNA of a monosaccharide transporter in rice, OsMST5 (Oryza sativa monosaccharide transporter 5) was cloned and its sugar transport activity was characterized by heterologous expression analysis. The amino acid sequence and topology were similar to the sequences and topology of other plant monosaccharide transporters. Yeast cells co-expressed with OsMST5 cDNA transported some monosaccharide substrates. The transport rate increased when ethanol as an electron donor was added, so the transporter was an energy-dependent active one. Most of the OsMST5 was expressed in panicles before pollination, indicating that it is associated with pollen development in rice.
Subject(s)
Monosaccharide Transport Proteins/genetics , Monosaccharide Transport Proteins/metabolism , Oryza/genetics , Oryza/metabolism , Amino Acid Sequence , Biological Transport , Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology , Cloning, Molecular , DNA, Complementary/genetics , Energy Metabolism , Ethanol/pharmacology , Hexoses/metabolism , Membrane Proteins/genetics , Models, Molecular , Molecular Sequence Data , Sequence Alignment , Sequence Homology, Amino Acid , Substrate Specificity , Yeasts/metabolismABSTRACT
Although the shoot apical meristem (SAM) is ultimately responsible for post-embryonic development in higher plants, lateral meristems also play an important role in determining the final morphology of the above-ground part. Axillary buds developing at the axils of leaves produce additional shoot systems, lateral branches. The rice TB1 gene (OsTB1) was first identified based on its sequence similarity with maize TEOSINTE BRANCHED 1 (TB1), which is involved in lateral branching in maize. Both genes encode putative transcription factors carrying a basic helix-loop-helix type of DNA-binding motif, named the TCP domain. The genetic locus of OsTB1 suggested that OsTB1 is a real counterpart of maize TB1. Transgenic rice plants overexpressing OsTB1 exhibited markedly reduced lateral branching without the propagation of axillary buds being affected. We also demonstrated that a rice strain carrying a classical morphological marker mutation, fine culm 1 (fc1), contain the loss-of-function mutation of OsTB1 and exhibits enhanced lateral branching. Expression of OsTB1, as examined with a putative promoter-glucuronidase (GUS) gene fusion, was observed throughout the axillary bud, as well as the basal part of the shoot apical meristem, vascular tissues in the pith and the lamina joint. Taking these data together, we concluded that OsTB1 functions as a negative regulator for lateral branching in rice, presumably through expression in axillary buds.