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    When ubiquitination meets phosphorylation: a systems biology perspective of EGFR/MAPK signalling

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    Authors
    Nguyen, Lan K
    Kolch, Walter
    Kholodenko, Boris N
    Issue Date
    2013-07-31
    Keywords
    GENETICS
    Local subject classification
    CELL BIOLOGY
    SYSTEMS BIOLOGY
    
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    Citation
    Cell Communication and Signaling. 2013 Jul 31;11(1):52
    URI
    http://dx.doi.org/10.1186/1478-811X-11-52
    http://hdl.handle.net/10147/299874
    Abstract
    Abstract Ubiquitination, the covalent attachment of ubiquitin to target proteins, has emerged as a ubiquitous post-translational modification (PTM) whose function extends far beyond its original role as a tag for protein degradation identified three decades ago. Although sharing parallel properties with phosphorylation, ubiquitination distinguishes itself in important ways. Nevertheless, the interplay and crosstalk between ubiquitination and phosphorylation events have become a recurrent theme in cell signalling regulation. Understanding how these two major PTMs intersect to regulate signal transduction is an important research question. In this review, we first discuss the involvement of ubiquitination in the regulation of the EGF-mediated ERK signalling pathway via the EGF receptor, highlighting the interplay between ubiquitination and phosphorylation in this cancer-implicated system and addressing open questions. The roles of ubiquitination in pathways crosstalking to EGFR/MAPK signalling will then be discussed. In the final part of the review, we demonstrate the rich and versatile dynamics of crosstalk between ubiquitination and phosphorylation by using quantitative modelling and analysis of network motifs commonly observed in cellular processes. We argue that given the overwhelming complexity arising from inter-connected PTMs, a quantitative framework based on systems biology and mathematical modelling is needed to efficiently understand their roles in cell signalling.
    Item Type
    Article
    Language
    en
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