Literature DB >> 27180904

Sterol-Rich Membrane Domains Define Fission Yeast Cell Polarity.

Tatyana Makushok1, Paulo Alves2, Stephen Michiel Huisman3, Adam Rafal Kijowski3, Damian Brunner4.   

Abstract

Cell polarization is crucial for the functioning of all organisms. The cytoskeleton is central to the process but its role in symmetry breaking is poorly understood. We study cell polarization when fission yeast cells exit starvation. We show that the basis of polarity generation is de novo sterol biosynthesis, cell surface delivery of sterols, and their recruitment to the cell poles. This involves four phases occurring independent of the polarity factor cdc42p. Initially, multiple, randomly distributed sterol-rich membrane (SRM) domains form at the plasma membrane, independent of the cytoskeleton and cell growth. These domains provide platforms on which the growth and polarity machinery assembles. SRM domains are then polarized by the microtubule-dependent polarity factor tea1p, which prepares for monopolar growth initiation and later switching to bipolar growth. SRM polarization requires F-actin but not the F-actin organizing polarity factors for3p and bud6p. We conclude that SRMs are key to cell polarization.
Copyright © 2016 Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27180904     DOI: 10.1016/j.cell.2016.04.037

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  14 in total

Review 1.  Polar localization of MreB actin is inhibited by anionic phospholipids in the rod-shaped bacterium Escherichia coli.

Authors:  Daisuke Shiomi
Journal:  Curr Genet       Date:  2017-04-24       Impact factor: 3.886

Review 2.  How do fission yeast cells grow and connect growth to the mitotic cycle?

Authors:  Ákos Sveiczer; Anna Horváth
Journal:  Curr Genet       Date:  2016-07-27       Impact factor: 3.886

3.  Hallmarks of Reversible Separation of Living, Unperturbed Cell Membranes into Two Liquid Phases.

Authors:  Scott P Rayermann; Glennis E Rayermann; Caitlin E Cornell; Alexey J Merz; Sarah L Keller
Journal:  Biophys J       Date:  2017-12-05       Impact factor: 4.033

Review 4.  Cell Polarity in Yeast.

Authors:  Jian-Geng Chiou; Mohan K Balasubramanian; Daniel J Lew
Journal:  Annu Rev Cell Dev Biol       Date:  2017-08-07       Impact factor: 13.827

5.  Electron donor cytochrome b5 is required for hyphal tip accumulation of sterol-rich plasma membrane domains and membrane fluidity in Aspergillus fumigatus.

Authors:  Chi Zhang; Yiran Ren; Lu Gao; Huiyu Gu; Ling Lu
Journal:  Appl Environ Microbiol       Date:  2020-11-30       Impact factor: 4.792

6.  Sphingolipid biosynthetic pathway is crucial for growth, biofilm formation and membrane integrity of Scedosporium boydii.

Authors:  Rodrigo Rollin-Pinheiro; Victor Pereira Rochetti; Mariana Ingrid Dutra da Silva Xisto; Livia Cristina Liporagi-Lopes; Beatriz Bastos; Antonella Rella; Ashutosh Singh; Sonia Rozental; Maurizio Del Poeta; Eliana Barreto-Bergter
Journal:  Future Med Chem       Date:  2019-11-12       Impact factor: 3.808

Review 7.  Cell polarity: Regulators and mechanisms in plants.

Authors:  Kezhen Yang; Lu Wang; Jie Le; Juan Dong
Journal:  J Integr Plant Biol       Date:  2020-01       Impact factor: 7.061

8.  Gradients of phosphatidylserine contribute to plasma membrane charge localization and cell polarity in fission yeast.

Authors:  Armin Haupt; Nicolas Minc
Journal:  Mol Biol Cell       Date:  2016-11-16       Impact factor: 4.138

9.  Sterol biosensor reveals LAM-family Ltc1-dependent sterol flow to endosomes upon Arp2/3 inhibition.

Authors:  Magdalena Marek; Vincent Vincenzetti; Sophie G Martin
Journal:  J Cell Biol       Date:  2020-06-01       Impact factor: 10.539

10.  Local and global Cdc42 guanine nucleotide exchange factors for fission yeast cell polarity are coordinated by microtubules and the Tea1-Tea4-Pom1 axis.

Authors:  Ye Dee Tay; Marcin Leda; Andrew B Goryachev; Kenneth E Sawin
Journal:  J Cell Sci       Date:  2018-07-19       Impact factor: 5.285

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