| Literature DB >> 27320200 |
Roberto Covino1, Stephanie Ballweg2, Claudius Stordeur2, Jonas B Michaelis2, Kristina Puth2, Florian Wernig2, Amir Bahrami1, Andreas M Ernst3, Gerhard Hummer1, Robert Ernst4.
Abstract
Maintaining a fluid bilayer is essential for cell signaling and survival. Lipid saturation is a key factor determining lipid packing and membrane fluidity, and it must be tightly controlled to guarantee organelle function and identity. A dedicated eukaryotic mechanism of lipid saturation sensing, however, remains elusive. Here we show that Mga2, a transcription factor conserved among fungi, acts as a lipid-packing sensor in the ER membrane to control the production of unsaturated fatty acids. Systematic mutagenesis, molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a pivotal role of the oligomeric transmembrane helix (TMH) of Mga2 for intra-membrane sensing, and they show that the lipid environment controls the proteolytic activation of Mga2 by stabilizing alternative rotational orientations of the TMH region. This work establishes a eukaryotic strategy of lipid saturation sensing that differs significantly from the analogous bacterial mechanism relying on hydrophobic thickness.Entities:
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Year: 2016 PMID: 27320200 DOI: 10.1016/j.molcel.2016.05.015
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970