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Identification of protein interactions of grapevine fanleaf virus RNA-dependent RNA polymerase during infection of Nicotiana benthamiana by affinity purification and tandem mass spectrometry

The RNA-dependent RNA polymerase (1E(Pol)) is involved in replication of grapevine fanleaf virus (GFLV, Nepovirus, Secoviridae) and causes vein clearing symptoms in Nicotiana benthamiana. Information on protein 1E(Pol) interaction with other viral and host proteins is scarce. To study protein 1E(Pol...

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Detalles Bibliográficos
Autores principales: Osterbaan, Larissa J., Hoyle, Victoria, Curtis, Michelle, DeBlasio, Stacy, Rivera, Keith D., Heck, Michelle, Fuchs, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295916/
https://www.ncbi.nlm.nih.gov/pubmed/34043500
http://dx.doi.org/10.1099/jgv.0.001607
Descripción
Sumario:The RNA-dependent RNA polymerase (1E(Pol)) is involved in replication of grapevine fanleaf virus (GFLV, Nepovirus, Secoviridae) and causes vein clearing symptoms in Nicotiana benthamiana. Information on protein 1E(Pol) interaction with other viral and host proteins is scarce. To study protein 1E(Pol) biology, three GFLV infectious clones, i.e. GHu (a symptomatic wild-type strain), GHu-1E(K802G) (an asymptomatic GHu mutant) and F13 (an asymptomatic wild-type strain), were engineered with protein 1E(Pol) fused to a V5 epitope tag at the C-terminus. Following Agrobacterium tumefaciens -mediated delivery of GFLV clones in N. benthamiana and protein extraction at seven dpi, when optimal 1E(Pol):V5 accumulation was detected, two viral and six plant putative interaction partners of V5-tagged protein 1E(Pol) were identified for the three GFLV clones by affinity purification and tandem mass spectrometry. This study provides insights into the protein interactome of 1E(Pol) during GFLV systemic infection in N. benthamiana and lays the foundation for validation work.