Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.celrep.2019.12.098
Title: Plasma Membrane Furrows Control Plasticity of ER-PM Contacts
Authors: Ng, A.Q.E.
Ng, A.Y.E.
Zhang, D. 
Issue Date: 2020
Publisher: Elsevier B.V.
Citation: Ng, A.Q.E., Ng, A.Y.E., Zhang, D. (2020). Plasma Membrane Furrows Control Plasticity of ER-PM Contacts. Cell Reports 30 (5) : 1434-14460000000. ScholarBank@NUS Repository. https://doi.org/10.1016/j.celrep.2019.12.098
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Ng et al. reveal a role of eisosome-coated plasma membrane (PM) furrows in regulating plasticity of endoplasmic reticulum (ER)-PM contacts. These sensory PM furrows function to strengthen local ER-PM association and attenuate tubular cER remodeling dynamics through electrostatic Scs2-Pil1 interactions. © 2019 The AuthorsThe plasma membrane (PM) forms extensive close junctions with the cortical endoplasmic reticulum (cER) in many cell types, ranging from yeast to mammals. How cells modulate structural plasticity of ER-PM contacts to accommodate space-demanding cortical events is largely unknown. Here, we report a role for eisosome-driven PM furrows in regulating ER-PM contact plasticity in fission yeast. We demonstrate that eisosome-coated PM invaginations function to stabilize local ER-PM contacts and attenuate cER remodeling dynamics through electrostatic Scs2-Pil1 interactions. We also identify divergent roles of ER-shaping proteins in controlling cER remodeling capacity and ER-PM contact plasticity. Furthermore, we show that eisosome organization is responsive to PM tension variations during active PM remodeling, which may enable adaptive control of ER-PM contact plasticity to potentially coordinate with space-demanding PM events. We thus propose a cellular strategy of modulating membrane contact plasticity by deploying sensory elements at contact sites. © 2019 The Authors
Source Title: Cell Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/198167
ISSN: 2211-1247
DOI: 10.1016/j.celrep.2019.12.098
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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