4.7 Article

Multiple Exocytotic Markers Accumulate at the Sites of Perifungal Membrane Biogenesis in Arbuscular Mycorrhizas

Journal

PLANT AND CELL PHYSIOLOGY
Volume 53, Issue 1, Pages 244-255

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/pcp/pcr170

Keywords

Daucus carota; Exocytosis; Medicago truncatula; Membrane dynamics; Plant-microbe interactions; Symbiosis

Funding

  1. University of Turin
  2. Italian National Project PRIN
  3. Regione Piemonte [CIPE-BioBITs]
  4. Czech Science Foundation [GACR_P305/11/1629]
  5. Ministry of Education, Youth and Sports (MSMT) [MSM0021620858]
  6. Netherlands Organization for Scientific Research (NWO)
  7. Russian Federation for Basic Research [047.018.001]

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Arbuscular mycorrhizas (AMs) are symbiotic interactions established within the roots of most plants by soil fungi belonging to the Glomeromycota. The extensive accommodation of the fungus in the root tissues largely takes place intracellularly, within a specialized interface compartment surrounded by the so-called perifungal membrane, an extension of the host plasmalemma. By combining live confocal imaging of green fluorescent protein (GFP)-tagged proteins and transmission electron microscopy (TEM), we have investigated the mechanisms leading to the biogenesis of this membrane. Our results show that pre-penetration responses and symbiotic interface construction are associated with extensive membrane dynamics. They involve the main components of the exocytotic machinery, with a major participation of the Golgi apparatus, as revealed by both TEM and in vivo GFP imaging. The labeling of known exocytosis markers, such as v-SNARE proteins of the VAMP72 family and the EXO84b subunit of the exocyst complex, allowed live imaging of the cell components involved in perifungal membrane construction, clarifying how this takes place ahead of the growing intracellular hypha. Lastly, our novel data are used to illustrate a model of membrane dynamics within the pre-penetration apparatus during AM fungal penetration.

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