Rowe Caitlin L, Wagstaff Kylie M, Oksayan Sibil, Glover Dominic J, Jans David A, Moseley Gregory W
Viral Pathogenesis Laboratory, Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, Victoria, Australia.
Nuclear Signaling Laboratory, Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.
PLoS One. 2016 Mar 3;11(3):e0150477. doi: 10.1371/journal.pone.0150477. eCollection 2016.
Rabies virus P-protein is expressed as five isoforms (P1-P5) which undergo nucleocytoplasmic trafficking important to roles in immune evasion. Although nuclear import of P3 is known to be mediated by an importin (IMP)-recognised nuclear localization sequence in the N-terminal region (N-NLS), the mechanisms underlying nuclear import of other P isoforms in which the N-NLS is inactive or has been deleted have remained unresolved. Based on the previous observation that mutation of basic residues K214/R260 of the P-protein C-terminal domain (P-CTD) can result in nuclear exclusion of P3, we used live cell imaging, protein interaction analysis and in vitro nuclear transport assays to examine in detail the nuclear trafficking properties of this domain. We find that the effect of mutation of K214/R260 on P3 is largely dependent on nuclear export, suggesting that nuclear exclusion of mutated P3 involves the P-CTD-localized nuclear export sequence (C-NES). However, assays using cells in which nuclear export is pharmacologically inhibited indicate that these mutations significantly inhibit P3 nuclear accumulation and, importantly, prevent nuclear accumulation of P1, suggestive of effects on NLS-mediated import activity in these isoforms. Consistent with this, molecular binding and transport assays indicate that the P-CTD mediates IMPα2/IMPβ1-dependent nuclear import by conferring direct binding to the IMPα2/IMPβ1 heterodimer, as well as to a truncated form of IMPα2 lacking the IMPβ-binding autoinhibitory domain (ΔIBB-IMPα2), and IMPβ1 alone. These properties are all dependent on K214 and R260. This provides the first evidence that P-CTD contains a genuine IMP-binding NLS, and establishes the mechanism by which P-protein isoforms other than P3 can be imported to the nucleus. These data underpin a refined model for P-protein trafficking that involves the concerted action of multiple NESs and IMP-binding NLSs, and highlight the intricate regulation of P-protein subcellular localization, consistent with important roles in infection.
狂犬病病毒P蛋白以五种异构体(P1 - P5)的形式表达,它们经历核质运输,这对免疫逃避作用很重要。虽然已知P3的核输入是由位于N端区域(N - NLS)的一种输入蛋白(IMP)识别的核定位序列介导的,但其他P异构体(其中N - NLS无活性或已被删除)的核输入机制仍未解决。基于先前的观察结果,即P蛋白C端结构域(P - CTD)的碱性残基K214/R260突变可导致P3的核排斥,我们使用活细胞成像、蛋白质相互作用分析和体外核运输测定来详细研究该结构域的核运输特性。我们发现K214/R260突变对P3的影响很大程度上取决于核输出,这表明突变型P3的核排斥涉及P - CTD定位的核输出序列(C - NES)。然而,使用药物抑制核输出的细胞进行的测定表明,这些突变显著抑制P3的核积累,重要的是,阻止P1的核积累,提示对这些异构体中NLS介导输入活性的影响。与此一致,分子结合和运输测定表明,P - CTD通过赋予与IMPα2/IMPβ1异二聚体以及缺乏IMPβ结合自抑制结构域的IMPα2截短形式(ΔIBB - IMPα2)和单独的IMPβ1直接结合来介导IMPα2/IMPβ1依赖性核输入。这些特性均依赖于K214和R260。这提供了第一个证据,即P - CTD包含一个真正的IMP结合NLS,并确立了除P3之外的P蛋白异构体可被导入细胞核的机制。这些数据支持了一个关于P蛋白运输的精细模型,该模型涉及多个NES和IMP结合NLS的协同作用,并突出了P蛋白亚细胞定位的复杂调控,这与感染中的重要作用一致。