The multivesicular body (MVB) pathway sorts ubiquitinated membrane cargo to intraluminal vesicles (ILVs) within the endosome, en route to the lysosomal lumen. The pathway involves the sequential action of conserved protein complexes [endosomal sorting complexes required for transport (ESCRTs)], culminating in the activation by ESCRT-II of ESCRT-III, a membrane-sculpting complex. Although this linear pathway of ESCRT activation is widely accepted, a study by Luzio and colleagues in a recent issue of the Biochemical Journal suggests that there is greater complexity in ESCRT-III activation, at least for some MVB cargoes. They show that ubiquitin-dependent sorting of major histocompatibility complex (MHC) class I to the MVB requires the central ESCRT-III complex but does not involve either ESCRT-II or functional links between ESCRT-II and ESCRT-III. Instead, they propose that MHC class I utilizes histidine-domain protein tyrosine phosphatase (HD-PTP), a non-canonical ESCRT interactor, to promote ESCRT-III activation.
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Showing TSPO transcriptional regulation cross-talk between hormone- and redox-sensitive signal transduction pathways. Courtesy of J. Gatliff and M. Campanella (see pages 107–121 for further details). - PDF Icon PDF LinkFront Matter
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Commentary|
January 05 2016
ESCRT-III on endosomes: new functions, new activation pathway
Philip Woodman
Philip Woodman
1
*Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, U.K.
1email [email protected]
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Publisher: Portland Press Ltd
Received:
October 22 2015
Accepted:
October 27 2015
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© 2016 Authors; published by Portland Press Limited
2016
Biochem J (2016) 473 (2): e5–e8.
Article history
Received:
October 22 2015
Accepted:
October 27 2015
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Citation
Philip Woodman; ESCRT-III on endosomes: new functions, new activation pathway. Biochem J 15 January 2016; 473 (2): e5–e8. doi: https://doi.org/10.1042/BJ20151115
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