Institute of Virology and Biotechnology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China.
Division of Structural Biology, Henry Wellcome Building, Roosevelt Drive, Oxford OX3 7BN, UK.
J Gen Virol. 2013 Sep;94(Pt 9):2117-2128. doi: 10.1099/vir.0.053256-0. Epub 2013 Jun 12.
Emaravirus is a recently described genus of negative-strand RNA plant viruses. Emaravirus P4 protein localizes to plasmodesmata, suggesting that it could be a viral movement protein (MP). In the current study, we showed that the P4 protein of raspberry leaf blotch emaravirus (RLBV) rescued the cell-to-cell movement of a defective potato virus X (PVX) that had a deletion mutation in the triple gene block 1 movement-associated protein. This demonstrated that RLBV P4 is a functional MP. Sequence analyses revealed that P4 is a distant member of the 30K superfamily of MPs. All MPs of this family contain two highly conserved regions predicted to form β-strands, namely β1 and β2. We explored by alanine mutagenesis the role of two residues of P4 (Ile106 and Asp127) located in each of these strands. We also made the equivalent substitutions in the 29K MP of tobacco rattle virus, another member of the 30K superfamily. All substitutions abolished the ability to complement PVX movement, except for the I106A substitution in the β1 region of P4. This region has been shown to mediate membrane association of 30K MPs; our results show that it is possible to make non-conservative substitutions of a well-conserved aliphatic residue within β1 without preventing the membrane association or movement function of P4.
埃玛拉病毒是一种新近被描述的负链 RNA 植物病毒属。埃玛拉病毒 P4 蛋白定位于胞间连丝,表明它可能是一种病毒运动蛋白(MP)。在本研究中,我们表明,覆盆子叶斑疹埃玛拉病毒(RLBV)的 P4 蛋白拯救了在三重基因块 1 运动相关蛋白缺失突变的缺陷马铃薯病毒 X(PVX)的细胞间运动。这表明 RLBV P4 是一种功能性 MP。序列分析表明,P4 是 30K MP 超家族的一个远亲。该家族的所有 MPs 都包含两个高度保守的区域,预计这两个区域将形成β-链,即β1 和β2。我们通过丙氨酸诱变探索了位于这些链中的 P4 的两个残基(Ile106 和 Asp127)的作用。我们还在烟草脆裂病毒的 29K MP 中进行了等效取代,烟草脆裂病毒是 30K 超家族的另一个成员。除了 P4 的β1 区域中的 I106A 取代之外,所有取代都消除了补充 PVX 运动的能力。该区域已被证明介导 30K MPs 的膜结合;我们的结果表明,在β1 中保守的脂族残基中进行非保守取代而不阻止 P4 的膜结合或运动功能是可能的。