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Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane
Phospholipases cleave phospholipids, major membrane constituents. They are thus essential for many developmental processes, including male gamete development. In flowering plants, mutation of phospholipase NOT-LIKE-DAD (NLD, also known as MTL or ZmPLA1) leads to peculiar defects in sexual reproducti...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327379/ https://www.ncbi.nlm.nih.gov/pubmed/34323919 http://dx.doi.org/10.1083/jcb.202010077 |
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author | Gilles, Laurine M. Calhau, Andrea R.M. La Padula, Veronica Jacquier, Nathanaël M.A. Lionnet, Claire Martinant, Jean-Pierre Rogowsky, Peter M. Widiez, Thomas |
author_facet | Gilles, Laurine M. Calhau, Andrea R.M. La Padula, Veronica Jacquier, Nathanaël M.A. Lionnet, Claire Martinant, Jean-Pierre Rogowsky, Peter M. Widiez, Thomas |
author_sort | Gilles, Laurine M. |
collection | PubMed |
description | Phospholipases cleave phospholipids, major membrane constituents. They are thus essential for many developmental processes, including male gamete development. In flowering plants, mutation of phospholipase NOT-LIKE-DAD (NLD, also known as MTL or ZmPLA1) leads to peculiar defects in sexual reproduction, notably the induction of maternal haploid embryos. Contrary to previous reports, NLD does not localize to cytosol and plasma membrane of sperm cells but to the pollen endo-plasma membrane (endo-PM), a specific membrane derived from the PM of the pollen vegetative cell that encircles the two sperm cells. After pollen tube burst, NLD localizes at the apical region of the egg apparatus. Pharmacological approaches coupled with targeted mutagenesis revealed that lipid anchoring together with electrostatic interactions are involved in the attachment of NLD to this atypical endo-PM. Membrane surface-charge and lipid biosensors indicated that phosphatidylinositol-4,5-bisphosphate is enriched in the endo-PM, uncovering a unique example of how membrane electrostatic properties can define a specific polar domain (i.e., endo-PM), which is critical for plant reproduction and gamete formation. |
format | Online Article Text |
id | pubmed-8327379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83273792022-04-04 Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane Gilles, Laurine M. Calhau, Andrea R.M. La Padula, Veronica Jacquier, Nathanaël M.A. Lionnet, Claire Martinant, Jean-Pierre Rogowsky, Peter M. Widiez, Thomas J Cell Biol Report Phospholipases cleave phospholipids, major membrane constituents. They are thus essential for many developmental processes, including male gamete development. In flowering plants, mutation of phospholipase NOT-LIKE-DAD (NLD, also known as MTL or ZmPLA1) leads to peculiar defects in sexual reproduction, notably the induction of maternal haploid embryos. Contrary to previous reports, NLD does not localize to cytosol and plasma membrane of sperm cells but to the pollen endo-plasma membrane (endo-PM), a specific membrane derived from the PM of the pollen vegetative cell that encircles the two sperm cells. After pollen tube burst, NLD localizes at the apical region of the egg apparatus. Pharmacological approaches coupled with targeted mutagenesis revealed that lipid anchoring together with electrostatic interactions are involved in the attachment of NLD to this atypical endo-PM. Membrane surface-charge and lipid biosensors indicated that phosphatidylinositol-4,5-bisphosphate is enriched in the endo-PM, uncovering a unique example of how membrane electrostatic properties can define a specific polar domain (i.e., endo-PM), which is critical for plant reproduction and gamete formation. Rockefeller University Press 2021-07-29 /pmc/articles/PMC8327379/ /pubmed/34323919 http://dx.doi.org/10.1083/jcb.202010077 Text en © 2021 Gilles et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Report Gilles, Laurine M. Calhau, Andrea R.M. La Padula, Veronica Jacquier, Nathanaël M.A. Lionnet, Claire Martinant, Jean-Pierre Rogowsky, Peter M. Widiez, Thomas Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title | Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title_full | Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title_fullStr | Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title_full_unstemmed | Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title_short | Lipid anchoring and electrostatic interactions target NOT-LIKE-DAD to pollen endo-plasma membrane |
title_sort | lipid anchoring and electrostatic interactions target not-like-dad to pollen endo-plasma membrane |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327379/ https://www.ncbi.nlm.nih.gov/pubmed/34323919 http://dx.doi.org/10.1083/jcb.202010077 |
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