4.6 Article

Sphingolipid biosynthesis modulates plasmodesmal ultrastructure and phloem unloading

Journal

NATURE PLANTS
Volume 5, Issue 6, Pages 604-615

Publisher

NATURE RESEARCH
DOI: 10.1038/s41477-019-0429-5

Keywords

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Categories

Funding

  1. Finnish Centre of Excellence in Molecular Biology of Primary Producers (Academy of Finland CoE program 2014-2019) [271832]
  2. Gatsby Foundation [GAT3395/PR3]
  3. National Science Foundation Biotechnology and Biological Sciences Research Council [BB/N013158/1]
  4. University of Helsinki [799992091]
  5. European Research Council Advanced Investigator Grant SYMDEV [323052]
  6. European Research Council under the European Union [772103-BRIDGING]
  7. Formation a la Recherche dans l'Industrie et l'Agriculture, Belgium [1.E.096.18]
  8. US Department of Energy Joint BioEnergy Institute - US Department of Energy, Office of Science, Office of Biological and Environmental Research [DE-AC02-05CH11231]
  9. Region Aquitaine [2011 13 04 007 PFM]
  10. [MetaboHUB-ANR-11-INBS-0010]
  11. BBSRC [BB/N013158/1] Funding Source: UKRI

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During phloem unloading, multiple cell-to-cell transport events move organic substances to the root meristem. Although the primary unloading event from the sieve elements to the phloem pole pericycle has been characterized to some extent, little is known about post-sieve element unloading. Here, we report a novel gene, PHLOEM UNLOADING MODULATOR (PLM), in the absence of which plasmodesmata-mediated symplastic transport through the phloem pole pericycle-endodermis interface is specifically enhanced. Increased unloading is attributable to a defect in the formation of the endoplasmic reticulum-plasma membrane tethers during plasmodesmal morphogenesis, resulting in the majority of pores lacking a visible cytoplasmic sleeve. PLM encodes a putative enzyme required for the biosynthesis of sphingolipids with very-long-chain fatty acid. Taken together, our results indicate that post-sieve element unloading involves sphingolipid metabolism, which affects plasmodesmal ultrastructure. They also raise the question of how and why plasmo-desmata with no cytoplasmic sleeve facilitate molecular trafficking.

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