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  Integrated Functions of Membrane Property Sensors and a Hidden Side of the Unfolded Protein Response

Covino, R., Hummer, G., & Ernst, R. (2018). Integrated Functions of Membrane Property Sensors and a Hidden Side of the Unfolded Protein Response. Molecular Cell, 71(3), 458-467. doi:10.1016/j.molcel.2018.07.019.

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 Creators:
Covino, Roberto1, Author           
Hummer, Gerhard1, 2, Author                 
Ernst, Robert3, Author
Affiliations:
1Department of Theoretical Biophysics, Max Planck Institute of Biophysics, Max Planck Society, ou_2068292              
2Institute of Biophysics, Goethe University, 60438 Frankfurt am Main, Germany, ou_persistent22              
3Department of Medical Biochemistry and Molecular Biology, Saarland University, Kirrberger Str. 100, Gebäude 61.4, 66421 Homburg, Germany, ou_persistent22              

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 Abstract: Eukaryotic cells face the challenge of maintaining the complex composition of several coexisting organelles. The molecular mechanisms underlying the homeostasis of subcellular membranes and their adaptation during stress are only now starting to emerge. Here, we discuss three membrane property sensors of the endoplasmic reticulum (ER), namely OPI1, MGA2, and IRE1, each controlling a large cellular program impacting the lipid metabolic network. OPI1 coordinates the production of membrane and storage lipids, MGA2 regulates the production of unsaturated fatty acids required for membrane biogenesis, and IRE1 controls the unfolded protein response (UPR) to adjust ER size, protein folding, and the secretory capacity of the cell. Although these proteins use remarkably distinct sensing mechanisms, they are functionally connected via the ER membrane and cooperate to maintain membrane homeostasis. As a rationalization of the recently described mechanism of UPR activation by lipid bilayer stress, we propose that IRE1 can sense the protein-to-lipid ratio in the ER membrane to ensure a balanced production of membrane proteins and lipids.

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Language(s): eng - English
 Dates: 20182018-08-022018-08-02
 Publication Status: Issued
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.molcel.2018.07.019
 Degree: -

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Title: Molecular Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 71 (3) Sequence Number: - Start / End Page: 458 - 467 Identifier: ISSN: 1097-2765
CoNE: https://pure.mpg.de/cone/journals/resource/954925610929