Lombardo Eleuterio, Ramírez Juan C, Garcia Javier, Almendral José M
Centro de Biología Molecular Severo Ochoa, (Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid), 28049 Cantoblanco, Madrid, Spain.
J Virol. 2002 Jul;76(14):7049-59. doi: 10.1128/jvi.76.14.7049-7059.2002.
This report describes the distribution of conventional nuclear localization sequences (NLS) and of a beta-stranded so-called nuclear localization motif (NLM) in the two proteins (VP1, 82 kDa; VP2, 63 kDa) forming the T=1 icosahedral capsid of the parvovirus minute virus of mice (MVM) and their functions in viral biogenesis and the onset of infection. The approximately 10 VP1 molecules assembled in the MVM particle harbor in its 142-amino-acid (aa) N-terminal-specific region four clusters of basic amino acids, here called BC1 (aa 6 to 10), BC2 (aa 87 to 90), BC3 (aa 109 to 115), and BC4 (aa 126 to 130), that fit consensus NLS and an NLM placed toward the opposite end of the polypeptide (aa 670 to 680) found to be necessary for VP2 nuclear uptake. Deletions and site-directed mutations constructed in an infectious MVM plasmid showed that BC1, BC2, and NLM are cooperative nuclear transport sequences in singly expressed VP1 subunits and that they conferred nuclear targeting competence on the VP1/VP2 oligomers arising in normal infection, while BC3 and BC4 did not display nuclear transport activity. Notably, VP1 proteins mutated at BC1 and -2, and particularly with BC1 to -4 sequences deleted, induced nuclear and cytoplasmic foci of colocalizing conjugated ubiquitin that could be rescued from the ubiquitin-proteasome degradation pathway by the coexpression of VP2 and NS2 isoforms. These results suggest a role for VP2 in viral morphogenesis by assisting cytoplasmic folding of VP1/VP2 subviral complexes, which is further supported by the capacity of NLM-bearing transport-competent VP2 subunits to recruit VP1 into the nuclear capsid assembly pathway regardless of the BC composition. Instead, all four BC sequences, which are located in the interior of the capsid, were absolutely required by the incoming infectious MVM particle for the onset of infection, suggesting either an important conformational change or a disassembly of the coat for nuclear entry of a VP1-associated viral genome. Therefore, the evolutionarily conserved BC sequences and NLM domains provide complementary nuclear transport functions to distinct supramolecular complexes of capsid proteins during the autonomous parvovirus life cycle.
本报告描述了常规核定位序列(NLS)以及一种β链状的所谓核定位基序(NLM)在构成小鼠细小病毒(MVM)T = 1二十面体衣壳的两种蛋白质(VP1,82 kDa;VP2,63 kDa)中的分布情况,以及它们在病毒生物发生和感染起始过程中的功能。组装在MVM颗粒中的约10个VP1分子在其142个氨基酸(aa)的N端特异性区域含有四个碱性氨基酸簇,这里称为BC1(aa 6至10)、BC2(aa 87至90)、BC3(aa 109至115)和BC4(aa 126至130),这些符合共有NLS,并且一个NLM位于多肽的另一端(aa 670至680),已发现该NLM对于VP2的核摄取是必需的。在感染性MVM质粒中构建的缺失和定点突变表明,BC1、BC2和NLM是单独表达的VP1亚基中的协同核转运序列,并且它们赋予了正常感染中产生的VP1/VP2寡聚体核靶向能力,而BC3和BC4未表现出核转运活性。值得注意的是,在BC1和-2处发生突变,特别是缺失BC1至-4序列的VP1蛋白,诱导了共定位的共轭泛素的核内和胞质聚集灶,通过VP2和NS2亚型的共表达可将其从泛素-蛋白酶体降解途径中拯救出来。这些结果表明VP2在病毒形态发生中通过协助VP1/VP2亚病毒复合物的胞质折叠发挥作用,这进一步得到了携带NLM的具有转运能力的VP2亚基能够将VP1募集到核衣壳组装途径中的能力的支持,而与BC组成无关。相反,位于衣壳内部的所有四个BC序列是进入的感染性MVM颗粒起始感染绝对必需的,这表明要么发生了重要的构象变化,要么衣壳解体以允许与VP1相关的病毒基因组进入细胞核。因此,在自主细小病毒生命周期中,进化上保守的BC序列和NLM结构域为衣壳蛋白的不同超分子复合物提供了互补的核转运功能。