Basyuk Eugenia, Galli Thierry, Mougel Marylène, Blanchard Jean-Marie, Sitbon Marc, Bertrand Edouard
IGMM-CNRS UMR5535, Université Montpellier II, IFR 24, 1919, route de Mende, 34293 Cedex 5, Montpellier, France.
Dev Cell. 2003 Jul;5(1):161-74. doi: 10.1016/s1534-5807(03)00188-6.
The viral genomes of alpha- and gamma-retroviruses follow an outbound route through the cytoplasm before assembling with the budding particle at the plasma membrane. We show here that murine leukemia virus (MLV) RNAs are transported on lysosomes and transferrin-positive endosomes. Transport on transferrin-positive vesicles requires both Gag and Env polyproteins. In the presence of Env, Gag is rerouted from lysosomes to transferrin-positive endosomes, and virion production becomes highly sensitive to drugs poisoning vesicular and endosomal traffic. Vesicular transport of the RNA does not require prior endocytosis, indicating that it is recruited directly from the cytosol. Viral prebudding complexes containing Env, Gag, and retroviral RNAs are thus formed on endosomes, and subsequently routed to the plasma membrane. This may allow retroviruses to hijack the endosomal machinery as part of their biosynthetic pathway. More generally, tethering to vesicles may provide an efficient mechanism for directed RNA transport.
α-和γ-逆转录病毒的病毒基因组在与质膜上的出芽颗粒组装之前,会通过细胞质遵循一条向外的路径。我们在此表明,小鼠白血病病毒(MLV)RNA通过溶酶体和转铁蛋白阳性内体进行运输。在转铁蛋白阳性囊泡上的运输需要Gag和Env多聚蛋白。在Env存在的情况下,Gag从溶酶体重新定向到转铁蛋白阳性内体,并且病毒体产生对毒害囊泡和内体运输的药物变得高度敏感。RNA的囊泡运输不需要预先的内吞作用,这表明它是直接从细胞质溶胶中募集的。因此,含有Env、Gag和逆转录病毒RNA的病毒出芽前复合物在内体上形成,随后被转运到质膜。这可能使逆转录病毒能够劫持内体机制作为其生物合成途径的一部分。更普遍地说,与囊泡的拴系可能为定向RNA运输提供一种有效的机制。