Plasmodesmal endoplasmic reticulum proteins regulate intercellular trafficking of cucumber mosaic virus in Arabidopsis

Author:

Ham Byung-Kook123ORCID,Wang Xiaohua4,Toscano-Morales Roberto3,Lin Jinxing4ORCID,Lucas William J3ORCID

Affiliation:

1. Global Institute for Food Security (GIFS), University of Saskatchewan , 421 Downey Rd, Saskatoon, SK S7N 4L8 , Canada

2. Department of Biology, University of Saskatchewan, 112 Science Place , Saskatoon, SK S7N 5E2 , Canada

3. Department of Plant Biology, College of Biological Sciences, University of California , Davis, CA 95616 , USA

4. Key Laboratory of Plant Resources, Institute of Botany, Chinese Academy of Sciences , Beijing 100093 , China

Abstract

Abstract Plasmodesmata (PD) are plasma membrane-lined cytoplasmic nanochannels that mediate cell-to-cell communication across the cell wall. A range of proteins are embedded in the PD plasma membrane and endoplasmic reticulum (ER), and function in regulating PD-mediated symplasmic trafficking. However, knowledge of the nature and function of the ER-embedded proteins in the intercellular movement of non-cell-autonomous proteins is limited. Here, we report the functional characterization of two ER luminal proteins, AtBiP1/2, and two ER integral membrane proteins, AtERdj2A/B, which are located within the PD. These PD proteins were identified as interacting proteins with cucumber mosaic virus (CMV) movement protein (MP) in co-immunoprecipitation studies using an Arabidopsis-derived plasmodesmal-enriched cell wall protein preparation (PECP). The AtBiP1/2 PD location was confirmed by TEM-based immunolocalization, and their AtBiP1/2 signal peptides (SPs) function in PD targeting. In vitro/in vivo pull-down assays revealed the association between AtBiP1/2 and CMV MP, mediated by AtERdj2A, through the formation of an AtBiP1/2–AtERdj2–CMV MP complex within PD. The role of this complex in CMV infection was established, as systemic infection was retarded in bip1/bip2w and erdj2b mutants. Our findings provide a model for a mechanism by which the CMV MP mediates cell-to-cell trafficking of its viral ribonucleoprotein complex.

Funder

National Institute of Food and Agriculture

National Science Foundation

Canada Foundation for Innovation

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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