Literature DB >> 25896017

Distribution of Sec24 isoforms to each ER exit site is dynamically regulated in Saccharomyces cerevisiae.

Hirohiko Iwasaki1, Tomohiro Yorimitsu1, Ken Sato2.   

Abstract

COPII vesicles are formed at specific subdomains of the ER, termed ER exit sites (ERESs). Depending on the cell type, ERESs number from a few to several hundred per cell. However, whether these ERESs are functionally and compositionally identical at the cellular level remains unclear. Our live cell-imaging analysis in Saccharomyces cerevisiae revealed that the isoforms of cargo-adaptor subunits are unequally distributed to each ERES at steady state, whereas this distribution is altered in response to UPR activation. These results suggest that in S. cerevisiae cargo loading to ERES is dynamically controlled in response to environmental changes.
Copyright © 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  COPII; ER exit site; Endoplasmic reticulum; Lst1; Sec24; UPR

Mesh:

Substances:

Year:  2015        PMID: 25896017     DOI: 10.1016/j.febslet.2015.04.006

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  9 in total

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Journal:  Mol Biol Cell       Date:  2019-12-18       Impact factor: 4.138

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9.  Trafficking of the amino acid transporter B0,+ (SLC6A14) to the plasma membrane involves an exclusive interaction with SEC24C for its exit from the endoplasmic reticulum.

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