Identification of arginine- and lysine-methylation in the proteome of Saccharomyces cerevisiae and its functional implications View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2010-12

AUTHORS

Chi Nam Ignatius Pang, Elisabeth Gasteiger, Marc R Wilkins

ABSTRACT

BACKGROUND: The methylation of eukaryotic proteins has been proposed to be widespread, but this has not been conclusively shown to date. In this study, we examined 36,854 previously generated peptide mass spectra from 2,607 Saccharomyces cerevisiae proteins for the presence of arginine and lysine methylation. This was done using the FindMod tool and 5 filters that took advantage of the high number of replicate analysis per protein and the presence of overlapping peptides. RESULTS: A total of 83 high-confidence lysine and arginine methylation sites were found in 66 proteins. Motif analysis revealed many methylated sites were associated with MK, RGG/RXG/RGX or WXXXR motifs. Functionally, methylated proteins were significantly enriched for protein translation, ribosomal biogenesis and assembly and organellar organisation and were predominantly found in the cytoplasm and ribosome. Intriguingly, methylated proteins were seen to have significantly longer half-life than proteins for which no methylation was found. Some 43% of methylated lysine sites were predicted to be amenable to ubiquitination, suggesting methyl-lysine might block the action of ubiquitin ligase. CONCLUSIONS: This study suggests protein methylation to be quite widespread, albeit associated with specific functions. Large-scale tandem mass spectroscopy analyses will help to further confirm the modifications reported here. More... »

PAGES

92

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1186/1471-2164-11-92

    DOI

    http://dx.doi.org/10.1186/1471-2164-11-92

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1051710342

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/20137074


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