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PMID: 21641804 Published · ppublish English Journal Article Review

Emerging roles for Lys11-linked polyubiquitin in cellular regulation.

Trends in biochemical sciences ·Vol. 36 ·No. 7 ·2011-07-00 ·Pages 355-63

Bremm A, Komander D

Abstract

Polyubiquitin chains are assembled via one of seven lysine (Lys) residues or the N terminus. The cellular roles of Lys48- and Lys63-linked polyubiquitin have been extensively studied; however, the cellular functions of Lys11-linked chains are less well understood. Recent insights into Lys11-linked ubiquitin chains have revealed their important function in cell cycle control. Additionally, Lys11 linkages have been identified in the context of mixed chains in many other cellular pathways. In this review, we introduce the specific enzymes that mediate Lys11-linked chain assembly and disassembly, and discuss the diverse cellular processes in which Lys11 linkages participate. Notably, mechanistic insights have revealed how the E2 ubiquitin-conjugating enzyme UBE2S achieves its Lys11 linkage specificity, and two structures of Lys11-linked polyubiquitin highlight the dynamic nature of this compact chain type.

MeSH Terms
Animals Endocytosis Endoplasmic Reticulum/genetics,metabolism Humans Lysine/chemistry,genetics,metabolism Polyubiquitin/chemistry,genetics,metabolism Signal Transduction Ubiquitins/genetics,metabolism
Chemicals
Ubiquitins Polyubiquitin Lysine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bremm Anja
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 0QH, UK.
Komander David
Article Info
Journal
Trends in biochemical sciences
Abbr.
Trends Biochem Sci
ISSN
0968-0004
Published
2011-07-00
Epub
2011-00-07
Pages
355-63
Language
English
Region
England
NLM ID
7610674
Subset
IM
Grants
Medical Research Council · MC_U105192732 · United Kingdom
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