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Regulation of Met1‐linked polyubiquitin signalling by the deubiquitinase OTULIN
Author(s) -
Elliott Paul R.,
Komander David
Publication year - 2016
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/febs.13547
Subject(s) - deubiquitinating enzyme , ubiquitin , transcription factor , signalling , microbiology and biotechnology , signal transduction , biology , regulator , wnt signaling pathway , biochemistry , chemistry , gene
Modification of proteins with Met1‐linked ‘linear’ ubiquitin chains has emerged as a key regulatory signal to control inflammatory signalling via the master regulator, the transcription factor nuclear factor κB ( NF ‐κB). While the assembly machinery, the linear ubiquitin chain assembly complex ( LUBAC ), and receptors for this ubiquitin chain type have been known for years, it was less clear which deubiquitinating enzymes ( DUB s) hydrolyse Met1 linkages specifically. In 2013, two labs reported the previously unannotated protein FAM 105B/ OTULIN to be this missing Met1 linkage‐specific DUB . Structural studies have revealed how OTULIN achieves its remarkable specificity, employing a mechanism of ubiquitin‐assisted catalysis in which a glutamate residue on the substrate complements the active site of the enzyme. The specificity of OTULIN enables it to regulate global levels of Met1‐linked polyubiquitin in cells. This ability led to investigations of NF ‐κB activation from new angles, and also revealed involvement of Met1‐polyubiquitin in Wnt signalling. Interestingly, OTULIN directly interacts with LUBAC , and this interaction is dynamic and can be regulated by OTULIN phosphorylation. This provides a new paradigm for how individual linkage types can be regulated by dedicated enzyme complexes mediating assembly and removal. Here we review what has been learned about OTULIN 's mechanism, regulation and function, discuss the open questions in the field, and discuss how DUB s regulate the NF ‐κB response.