Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, NY 11944, USA.
Virology. 2011 Mar 30;412(1):68-74. doi: 10.1016/j.virol.2010.12.060. Epub 2011 Jan 23.
Here we show that IQGAP1, a cellular protein that plays a pivotal role as a regulator of the cytoskeleton interacts with Classical Swine Fever Virus (CSFV) Core protein. Sequence analyses identified residues within CSFV Core protein (designated as areas I, II, III and IV) that maintain homology to regions within the matrix protein of Moloney Murine Leukemia Virus (MMLV) that mediate binding to IQGAP1 [EMBO J, 2006 25:2155]. Alanine-substitution within Core regions I, II, III and IV identified residues that specifically mediate the Core-IQGAP1 interaction. Recombinant CSFV viruses harboring alanine substitutions at residues (207)ATI(209) (I), (210)VVE(212) (II), (213)GVK(215) (III), or (232)GLYHN(236) (IV) have defective growth in primary swine macrophage cultures. In vivo, substitutions of residues in areas I and III yielded viruses that were completely attenuated in swine. These data shows that the interaction of Core with an integral component of cytoskeletal regulation plays a role in the CSFV cycle.
在这里,我们展示了 IQGAP1,一种作为细胞骨架调节剂发挥关键作用的细胞蛋白,与经典猪瘟病毒(CSFV)核心蛋白相互作用。序列分析鉴定出 CSFV 核心蛋白中的残基(指定为区域 I、II、III 和 IV),这些残基与 Moloney 鼠白血病病毒(MMLV)基质蛋白中的区域保持同源性,介导与 IQGAP1 的结合[EMBO J,2006 25:2155]。在核心区域 I、II、III 和 IV 中进行丙氨酸取代鉴定出特异性介导核心-IQGAP1 相互作用的残基。在残基 (207)ATI(209)(I)、(210)VVE(212)(II)、(213)GVK(215)(III)或 (232)GLYHN(236)(IV)处携带丙氨酸取代的重组 CSFV 病毒在原代猪巨噬细胞培养物中的生长受到缺陷。在体内,区域 I 和 III 中的残基取代产生的病毒在猪中完全减毒。这些数据表明,核心与细胞骨架调节的组成部分的相互作用在 CSFV 周期中发挥作用。