The ex planta signal activity of a Medicago ribosomal uL2 protein suggests a moonlighting role in controlling secondary rhizobial infection.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 27 02 2020
accepted: 15 06 2020
entrez: 1 10 2020
pubmed: 2 10 2020
medline: 13 11 2020
Statut: epublish

Résumé

We recently described a regulatory loop, which we termed autoregulation of infection (AOI), by which Sinorhizobium meliloti, a Medicago endosymbiont, downregulates the root susceptibility to secondary infection events via ethylene. AOI is initially triggered by so-far unidentified Medicago nodule signals named signal 1 and signal 1' whose transduction in bacteroids requires the S. meliloti outer-membrane-associated NsrA receptor protein and the cognate inner-membrane-associated adenylate cyclases, CyaK and CyaD1/D2, respectively. Here, we report on advances in signal 1 identification. Signal 1 activity is widespread as we robustly detected it in Medicago nodule extracts as well as in yeast and bacteria cell extracts. Biochemical analyses indicated a peptidic nature for signal 1 and, together with proteomic analyses, a universally conserved Medicago ribosomal protein of the uL2 family was identified as a candidate signal 1. Specifically, MtRPuL2A (MtrunA17Chr7g0247311) displays a strong signal activity that requires S. meliloti NsrA and CyaK, as endogenous signal 1. We have shown that MtRPuL2A is active in signaling only in a non-ribosomal form. A Medicago truncatula mutant in the major symbiotic transcriptional regulator MtNF-YA1 lacked most signal 1 activity, suggesting that signal 1 is under developmental control. Altogether, our results point to the MtRPuL2A ribosomal protein as the candidate for signal 1. Based on the Mtnf-ya1 mutant, we suggest a link between root infectiveness and nodule development. We discuss our findings in the context of ribosomal protein moonlighting.

Identifiants

pubmed: 33002000
doi: 10.1371/journal.pone.0235446
pii: PONE-D-20-05716
pmc: PMC7529298
doi:

Substances chimiques

Ethylenes 0
Plant Proteins 0
Ribosomal Proteins 0
ethylene 91GW059KN7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0235446

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist

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Auteurs

Fernando Sorroche (F)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Violette Morales (V)

Laboratoire de Microbiologie et de Génétique Moléculaires, UMR5100, Centre de Biologie Intégrative (CBI), Centre National de la Recherche Scientifique (CNRS), Université de Toulouse, UPS, Toulouse, France.

Saïda Mouffok (S)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Carole Pichereaux (C)

Fédération de Recherche (FR3450), Agrobiosciences, Interactions et Biodiversité (AIB), CNRS, Toulouse, France.
Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse UPS, CNRS, Toulouse, France.

A Marie Garnerone (AM)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Lan Zou (L)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Badrish Soni (B)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Marie-Anne Carpéné (MA)

I2MC, Université de Toulouse UPS, INSERM, CNRS, Toulouse, France.

Audrey Gargaros (A)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse UPS, CNRS, Toulouse, France.

Fabienne Maillet (F)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Odile Burlet-Schiltz (O)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse UPS, CNRS, Toulouse, France.

Verena Poinsot (V)

I2MC, Université de Toulouse UPS, INSERM, CNRS, Toulouse, France.

Patrice Polard (P)

Laboratoire de Microbiologie et de Génétique Moléculaires, UMR5100, Centre de Biologie Intégrative (CBI), Centre National de la Recherche Scientifique (CNRS), Université de Toulouse, UPS, Toulouse, France.

Clare Gough (C)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

Jacques Batut (J)

Laboratoire des Interactions Plantes Microorganismes (LIPM), INRAE, CNRS, Castanet-Tolosan, France.

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