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The functional diversity of protein lysine methylation

Large‐scale characterization of post‐translational modifications (PTMs), such as phosphorylation, acetylation and ubiquitination, has highlighted their importance in the regulation of a myriad of signaling events. While high‐throughput technologies have tremendously helped cataloguing the proteins m...

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Autores principales: Lanouette, Sylvain, Mongeon, Vanessa, Figeys, Daniel, Couture, Jean‐François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023394/
https://www.ncbi.nlm.nih.gov/pubmed/24714364
http://dx.doi.org/10.1002/msb.134974
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author Lanouette, Sylvain
Mongeon, Vanessa
Figeys, Daniel
Couture, Jean‐François
author_facet Lanouette, Sylvain
Mongeon, Vanessa
Figeys, Daniel
Couture, Jean‐François
author_sort Lanouette, Sylvain
collection PubMed
description Large‐scale characterization of post‐translational modifications (PTMs), such as phosphorylation, acetylation and ubiquitination, has highlighted their importance in the regulation of a myriad of signaling events. While high‐throughput technologies have tremendously helped cataloguing the proteins modified by these PTMs, the identification of lysine‐methylated proteins, a PTM involving the transfer of one, two or three methyl groups to the ε‐amine of a lysine side chain, has lagged behind. While the initial findings were focused on the methylation of histone proteins, several studies have recently identified novel non‐histone lysine‐methylated proteins. This review provides a compilation of all lysine methylation sites reported to date. We also present key examples showing the impact of lysine methylation and discuss the circuitries wired by this important PTM.
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spelling pubmed-40233942014-05-16 The functional diversity of protein lysine methylation Lanouette, Sylvain Mongeon, Vanessa Figeys, Daniel Couture, Jean‐François Mol Syst Biol Review Large‐scale characterization of post‐translational modifications (PTMs), such as phosphorylation, acetylation and ubiquitination, has highlighted their importance in the regulation of a myriad of signaling events. While high‐throughput technologies have tremendously helped cataloguing the proteins modified by these PTMs, the identification of lysine‐methylated proteins, a PTM involving the transfer of one, two or three methyl groups to the ε‐amine of a lysine side chain, has lagged behind. While the initial findings were focused on the methylation of histone proteins, several studies have recently identified novel non‐histone lysine‐methylated proteins. This review provides a compilation of all lysine methylation sites reported to date. We also present key examples showing the impact of lysine methylation and discuss the circuitries wired by this important PTM. European Molecular Biology Organization 2014-04-08 /pmc/articles/PMC4023394/ /pubmed/24714364 http://dx.doi.org/10.1002/msb.134974 Text en © 2014 EMBO This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Lanouette, Sylvain
Mongeon, Vanessa
Figeys, Daniel
Couture, Jean‐François
The functional diversity of protein lysine methylation
title The functional diversity of protein lysine methylation
title_full The functional diversity of protein lysine methylation
title_fullStr The functional diversity of protein lysine methylation
title_full_unstemmed The functional diversity of protein lysine methylation
title_short The functional diversity of protein lysine methylation
title_sort functional diversity of protein lysine methylation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023394/
https://www.ncbi.nlm.nih.gov/pubmed/24714364
http://dx.doi.org/10.1002/msb.134974
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