Soond, Surinder M. and Chantry, Andrew (2011) How ubiquitination regulates the TGF-β signalling pathway: New insights and new players. BioEssays, 33 (10). pp. 749-758. ISSN 1521-1878
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Abstract
Ubiquitination of protein species in regulating signal transduction pathways is universally accepted as of fundamental importance for normal development, and defects in this process have been implicated in the progression of many human diseases. One pathway that has received much attention in this context is transforming growth factor-beta (TGF-ß) signalling, particularly during the regulation of epithelial-mesenchymal transition (EMT) and tumour progression. While E3-ubiquitin ligases offer themselves as potential therapeutic targets, much remains to be unveiled regarding mechanisms that culminate in their regulation. With this in mind, the focus of this review highlights the regulation of the ubiquitination pathway and the significance of a recently described group of NEDD4 E3-ubiquitin ligase isoforms in the context of TGF-ß pathway regulation. Moreover, we now broaden these observations to incorporate a growing number of protein isoforms within the ubiquitin ligase superfamily as a whole, and discuss their relevance in defining a new ‘iso-ubiquitinome’.
Item Type: | Article |
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Uncontrolled Keywords: | sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being |
Faculty \ School: | Faculty of Science > School of Biological Sciences |
UEA Research Groups: | Faculty of Science > Research Groups > Cells and Tissues |
Depositing User: | Users 2731 not found. |
Date Deposited: | 10 Jan 2012 14:52 |
Last Modified: | 21 Apr 2023 23:48 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/36056 |
DOI: | 10.1002/bies.201100057 |
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