A high‐confidence Physcomitrium patens plasmodesmata proteome by iterative scoring and validation reveals diversification of cell wall proteins during evolution

Author:

Gombos Sven1ORCID,Miras Manuel2ORCID,Howe Vicky3ORCID,Xi Lin1ORCID,Pottier Mathieu2ORCID,Kazemein Jasemi Neda S.3ORCID,Schladt Moritz2ORCID,Ejike J. Obinna2ORCID,Neumann Ulla4ORCID,Hänsch Sebastian5ORCID,Kuttig Franziska3,Zhang Zhaoxia1,Dickmanns Marcel26ORCID,Xu Peng6,Stefan Thorsten1,Baumeister Wolfgang6ORCID,Frommer Wolf B.27ORCID,Simon Rüdiger3ORCID,Schulze Waltraud X.1ORCID

Affiliation:

1. Department of Plant Systems Biology University of Hohenheim 70593 Stuttgart Germany

2. Department of Molecular Physiology Heinrich Heine University of Düsseldorf 40225 Düsseldorf Germany

3. Department of Developmental Genetics Heinrich Heine University of Düsseldorf 40225 Düsseldorf Germany

4. Central Microscopy Max Planck Institute for Plant Breeding Research 50829 Cologne Germany

5. Center for Advanced Imaging Heinrich Heine University of Düsseldorf 40225 Düsseldorf Germany

6. Department of Molecular Structural Biology Max Planck Institute of Biochemistry 82152 Martinsried Germany

7. Institute for Transformative Biomolecules Nagoya University Nagoya 464-0813 Japan

Abstract

Summary Plasmodesmata (PD) facilitate movement of molecules between plant cells. Regulation of this movement is still not understood. Plasmodesmata are hard to study, being deeply embedded within cell walls and incorporating several membrane types. Thus, structure and protein composition of PD remain enigmatic. Previous studies of PD protein composition identified protein lists with few validations, making functional conclusions difficult. We developed a PD scoring approach in iteration with large‐scale systematic localization, defining a high‐confidence PD proteome of Physcomitrium patens (HC300). HC300, together with bona fide PD proteins from literature, were placed in Pddb. About 65% of proteins in HC300 were not previously PD‐localized. Callose‐degrading glycolyl hydrolase family 17 (GHL17) is an abundant protein family with representatives across evolutionary scale. Among GHL17s, we exclusively found members of one phylogenetic clade with PD localization and orthologs occur only in species with developed PD. Phylogenetic comparison was expanded to xyloglucan endotransglucosylases/hydrolases and Exordium‐like proteins, which also diversified into PD‐localized and non‐PD‐localized members on distinct phylogenetic clades. Our high‐confidence PD proteome HC300 provides insights into diversification of large protein families. Iterative and systematic large‐scale localization across plant species strengthens the reliability of HC300 as basis for exploring structure, function, and evolution of this important organelle.

Funder

H2020 European Research Council

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Plant Science,Physiology

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