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

被引:76
作者
Genre, A. [1 ]
Ivanov, S. [2 ]
Fendrych, M. [3 ]
Faccio, A. [4 ]
Zarsky, V. [5 ]
Bisseling, T. [2 ]
Bonfante, P. [1 ]
机构
[1] Univ Turin, Dept Plant Biol, I-10125 Turin, Italy
[2] Wageningen Univ, Mol Biol Lab, Dept Plant Sci, NL-6708 PB Wageningen, Netherlands
[3] Acad Sci Czech Republ, Inst Expt Bot, CR-16502 Prague 6, Czech Republic
[4] IPP CNR, I-10125 Turin, Italy
[5] Charles Univ Prague, Dept Expt Plant Biol, Fac Sci, CR-12844 Prague 2, Czech Republic
关键词
Daucus carota; Exocytosis; Medicago truncatula; Membrane dynamics; Plant-microbe interactions; Symbiosis; ROOT EPIDERMAL-CELLS; MEDICAGO-TRUNCATULA; PLANT-CELL; EXOCYST COMPLEX; FUNGI; ARABIDOPSIS; INFECTION; REVEALS; INTERFACE; RESPONSES;
D O I
10.1093/pcp/pcr170
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:244 / 255
页数:12
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