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K27-linked ubiquitylation promotes p97 substrate processing and is essential for cell proliferation

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Item Type:Article
Title:K27-linked ubiquitylation promotes p97 substrate processing and is essential for cell proliferation
Creators Name:Shearer, R.F. and Typas, D. and Coscia, F. and Schovsbo, S. and Kruse, T. and Mund, A. and Mailand, N.
Abstract:Conjugation of ubiquitin (Ub) to numerous substrate proteins regulates virtually all cellular processes. Eight distinct ubiquitin polymer linkages specifying different functional outcomes are generated in cells. However, the roles of some atypical poly-ubiquitin topologies, in particular linkages via lysine 27 (K27), remain poorly understood due to a lack of tools for their specific detection and manipulation. Here, we adapted a cell-based ubiquitin replacement strategy to enable selective and conditional abrogation of K27-linked ubiquitylation, revealing that this ubiquitin linkage type is essential for proliferation of human cells. We demonstrate that K27-linked ubiquitylation is predominantly a nuclear modification whose ablation deregulates nuclear ubiquitylation dynamics and impairs cell cycle progression in an epistatic manner with inactivation of the ATPase p97/VCP. Moreover, we show that a p97-proteasome pathway model substrate (Ub(G76V)-GFP) is directly modified by K27-linked ubiquitylation, and that disabling the formation of K27-linked ubiquitin signals or blocking their decoding via overexpression of the K27 linkage-specific binder UCHL3 impedes Ub(G76V)-GFP turnover at the level of p97 function. Our findings suggest a critical role of K27-linked ubiquitylation in supporting cell fitness by facilitating p97-dependent processing of ubiquitylated nuclear proteins.
Keywords:Cell Cycle, K27-Linked Ubiquitylation, p97/VCP, Ubiquitin, Ubiquitin-Proteasome System
Source:EMBO Journal
ISSN:0261-4189
Publisher:EMBO Press / Wiley
Volume:41
Number:9
Page Range:e110145
Date:2 May 2022
Official Publication:https://doi.org/10.15252/embj.2021110145
PubMed:View item in PubMed

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