Anti-RPL3 polyclonal antibody

Secondary metabolites produced by pathogens during the infection process are thought to play a role as pathogenicity or virulence determinants in many plant diseases. Baker's yeast and the plant Arabidopsis thaliana are attractive models for elucidating molecular mechanisms of resistance to toxic substances. For the Fusarium mycotoxin deoxynivalenol, the following resistance mechanisms were identified in yeast: (1) reduced toxin uptake due to the ABC transporter protein Pdr5p (molecular efflux pump), (2) detoxification by the acetyltransferase Ayt1p, and (3) modification of the ribosomal target by amino acid changes in the ribosomal protein L3 (Rp13p). PDR5-like genes exist in plant genomes as large gene families and could play an important role as a first line of defence against a broad range of toxic metabolites. Amino acid alterations in the highly conserved RPL3 genes could likewise play a role in trichothecene resistance in plants. The knowledge obtained using model systems should be valuable in biotechnological approaches to disease control and marker-assisted resistance breeding.

Protein histidine methylation is a rarely studied posttranslational modification in eukaryotes. Although the presence of N-methylhistidine was demonstrated in actin in the early 1960s, so far, only a limited number of proteins containing N-methylhistidine have been reported, including S100A9, myosin, skeletal muscle myosin light chain kinase (MLCK 2), and ribosomal protein Rpl3. Furthermore, the role of histidine methylation in the functioning of the protein and in cell physiology remains unclear due to a shortage of studies focusing on this topic. However, the molecular identification of the first two distinct histidine-specific protein methyltransferases has been established in yeast (Hpm1) and in metazoan species (actin-histidine N-methyltransferase), giving new insights into the phenomenon of protein methylation at histidine sites. As a result, we are now beginning to recognize protein histidine methylation as an important regulatory mechanism of protein functioning whose loss may have deleterious consequences in both cells and in organisms. In this review, we aim to summarize the recent advances in the understanding of the chemical, enzymological, and physiological aspects of protein histidine methylation.