Wakana, Y. and Takai, S. and Nakajima, K. -I. and Tani, K. and Yamamoto, A. and Watson, P. and Stephens, D. J. and Hauri, H. -P. and Tagaya, M.. (2008) Bap31 is an itinerant protein that moves between the peripheral endoplasmic reticulum (ER) and a juxtanuclear compartment related to ER-associated Degradation. Molecular Biology of the Cell, 19 (5). pp. 1825-1836.
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Official URL: http://edoc.unibas.ch/dok/A5257734
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Abstract
Certain endoplasmic reticulum (ER)-associated degradation (ERAD) substrates with transmembrane domains are segregated from other ER proteins and sorted into a juxtanuclear subcompartment, known as the ER quality control compartment. Bap31 is an ER protein with three transmembrane domains, and it is assumed to be a cargo receptor for ER export of some transmembrane proteins, especially those prone to ERAD. Here, we show that Bap31 is a component of the ER quality control compartment and that it moves between the peripheral ER and a juxtanuclear ER or ER-related compartment distinct from the conventional ER-Golgi intermediate compartment. The third and second transmembrane domains of Bap31 are principally responsible for the movement to and recycling from the juxtanuclear region, respectively. This cycling was blocked by depolymerization of microtubules and disruption of dynein-dynactin function. Overexpression of Sar1p and Arf1 mutants affected Bap31 cycling, suggesting that this cycling pathway is related to the conventional vesicular transport pathways.
Faculties and Departments: | 05 Faculty of Science > Departement Biozentrum > Former Organization Units Biozentrum > Pharmacology/Neurobiology (Hauri) |
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UniBasel Contributors: | Hauri, Hans-Peter |
Item Type: | Article, refereed |
Article Subtype: | Research Article |
Publisher: | American Society for Cell Biology |
ISSN: | 1059-1524 |
e-ISSN: | 1939-4586 |
Note: | Publication type according to Uni Basel Research Database: Journal article |
Language: | English |
Identification Number: | |
edoc DOI: | |
Last Modified: | 07 Nov 2017 08:03 |
Deposited On: | 22 Mar 2012 13:18 |
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