The potato virus x TGBp2 protein association with the endoplasmic reticulum plays a role in but is not sufficient for viral cell-to-cell movement

• Published in: Virology (New York, N.Y.) N.Y.), 2003-07, Vol.312 (1), p.35-48
• Main Authors: Mitra, Ruchira, Krishnamurthy, Konduru, Blancaflor, Elison, Payton, Mark, Nelson, Richard S, Verchot-Lubicz, Jeanmarie
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Endoplasmic Reticulum - metabolism; Gene Expression Regulation, Viral; Green Fluorescent Proteins; Life Sciences (General); Luminescent Proteins; Molecular Sequence Data; Movement; Mutation; Nicotiana - cytology; Nicotiana - metabolism; Nicotiana - virology; Plant Leaves - cytology; Plant Leaves - metabolism; Plant Leaves - virology; Plants, Genetically Modified; Potexvirus - genetics; Potexvirus - physiology; Protein Transport; Sequence Alignment; Solanum tuberosum - virology; Viral Proteins - chemistry; Viral Proteins - genetics; Viral Proteins - metabolism
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/S0042-6822(03)00180-6

Potato virus X (PVX) TGBp1, TGBp2, TGBp3, and coat protein are required for virus cell-to-cell movement. Plasmids expressing GFP fused to TGBp2 were bombarded to leaf epidermal cells and GFP:TGBp2 moved cell to cell in Nicotiana benthamiana leaves but not in Nicotiana tabacum leaves. GFP:TGBp2 movement was observed in TGBp1-transgenic N. tabacum, indicating that TGBp2 requires TGBp1 to promote its movement in N. tabacum. In this study, GFP:TGBp2 was detected in a polygonal pattern that resembles the endoplasmic reticulum (ER) network. Amino acid sequence analysis revealed TGBp2 has two putative transmembrane domains. Two mutations separately introduced into the coding sequences encompassing the putative transmembrane domains within the GFP:TGBp2 plasmids and PVX genome, disrupted membrane binding of GFP:TGBp2, inhibited GFP:TGBp2 movement in N. benthamiana and TGBp1-expressing N. tabacum, and inhibited PVX movement. A third mutation, lying outside the transmembrane domains, had no effect on GFP:TGBp2 ER association or movement in N. benthamiana but inhibited GFP:TGBp2 movement in TGBp1-expressing N. tabacum and PVX movement in either Nicotiana species. Thus, ER association of TGBp2 may be required but not be sufficient for virus movement. TGBp2 likely provides an activity for PVX movement beyond ER association.