Basyuk Eugenia, Boulon Séverine, Skou Pedersen Finn, Bertrand Edouard, Vestergaard Rasmussen Søren
IGMM-CNRS UMR5535, IFR 24, 1919, route de Mende 34293 Montpellier Cedex 5, France.
J Mol Biol. 2005 Nov 25;354(2):330-9. doi: 10.1016/j.jmb.2005.09.071. Epub 2005 Oct 10.
Packaging of MLV genomes requires four cis-acting stem-loops. Stem-loops A and B are self-complementary and bind Gag in their dimeric form, while the C and D elements mediate loop-loop interactions that facilitate RNA dimerization. Packaging also requires nuclear export of viral genomes, and their cytoplasmic transport toward the plasma membrane. For MLV, this is mediated by Gag and Env, and occurs on endosomal vesicles. Here, we report that MLV Psi acts at several steps during the transport of genomic RNAs. First, deletion of stem-loop B or C leads to the accumulation of genomic RNAs in the nucleus, suggesting that these elements are involved in export. Second, in chronically infected cells, mutation of the C and D loops impairs endosomal transport. This suggests that RNA dimerization is essential for vesicular transport, consistent with its proposed requirement for Gag binding. Surprisingly, deletion of stem-loop A blocks vesicular transport, whereas removal of stem-loop B has no effects. This suggests that stem-loop A has unique functions in packaging, not predicted from previous in vitro analyses. Finally, in packaging cells that do not express any Psi-containing RNA, endosomal RNA transport becomes sequence-independent. This non-specific activity of Gag likely promotes packaging of cellular mRNAs.
莫洛尼鼠白血病病毒(MLV)基因组的包装需要四个顺式作用茎环。茎环A和B是自我互补的,以二聚体形式结合Gag,而C和D元件介导促进RNA二聚化的环-环相互作用。包装还需要病毒基因组的核输出及其向质膜的细胞质运输。对于MLV来说,这是由Gag和Env介导的,发生在内体小泡上。在此,我们报告MLV的ψ在基因组RNA运输过程中的几个步骤发挥作用。首先,茎环B或C的缺失导致基因组RNA在细胞核中积累,这表明这些元件参与了输出。其次,在慢性感染细胞中,C和D环的突变会损害内体运输。这表明RNA二聚化对于小泡运输至关重要,与其对Gag结合的假定要求一致。令人惊讶的是,茎环A的缺失会阻断小泡运输,而茎环B的去除则没有影响。这表明茎环A在包装中具有独特功能,这是先前体外分析未预测到的。最后,在不表达任何含ψRNA的包装细胞中,内体RNA运输变得不依赖序列。Gag的这种非特异性活性可能促进细胞mRNA的包装。