Artículo

Laccaria bicolor MiSSP8 is a small-secreted protein decisive for the establishment of the ectomycorrhizal symbiosis

Pellegrin, Clément ; Pellegrin, Clément ; Ruytinx, Joske ; Guinet, Frédéric ; Kemppainen, Minna Johanna Icon; Frei dit Frey, Nicolas ; Puech Pagès, Virginie ; Hecker, Arnaud ; Pardo, Alejandro Guillermo Icon; Martin, Francis M. ; Veneault Fourrey, Claire

Otros responsables

Fecha

10/2019

Editorial

Wiley Blackwell Publishing, Inc

Revista

Environmental Microbiology

Título del libro

Nombre del evento

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Institución organizadora

ISSN

1462-2912

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

The ectomycorrhizal symbiosis is a predominant tree–microbe interaction in forest ecosystems sustaining tree growth and health. Its establishment and functioning implies a long‐term and intimate relationship between the soil‐borne fungi and the roots of trees. Mycorrhiza‐induced Small‐Secreted Proteins (MiSSPs) are hypothesized as keystone symbiotic proteins, required to set up the symbiosis by modifying the host metabolism and/or building the symbiotic interfaces. L. bicolor MiSSP8 is the third most highly induced MiSSPs in symbiotic tissues and it is also expressed in fruiting bodies. The MiSSP8‐RNAi knockdown mutants are strongly impaired in their mycorrhization ability with Populus, with the lack of fungal mantle and Hartig net development due to the lack of hyphal aggregation. MiSSP8 C‐terminus displays a repetitive motif containing a kexin cleavage site, recognized by KEX2 in vitro. This suggests MiSSP8 protein might be cleaved into small peptides. Moreover, the MiSSP8 repetitive motif is found in other proteins predicted secreted by both saprotrophic and ectomycorrhizal fungi. Thus, our data indicate that MiSSP8 is a small‐secreted protein involved at early stages of ectomycorrhizal symbiosis, likely by regulating hyphal aggregation and pseudoparenchyma formation.

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