Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, Canada.
PLoS Pathog. 2010 Jul 8;6(7):e1000984. doi: 10.1371/journal.ppat.1000984.
Ribonucleotide reductases (RRs) are evolutionarily-conserved enzymes that catalyze the rate-limiting step during dNTP synthesis in mammals. RR consists of both large (R1) and small (R2) subunits, which are both required for catalysis by the R1(2)R2(2) heterotetrameric complex. Poxviruses also encode RR proteins, but while the Orthopoxviruses infecting humans [e.g. vaccinia (VACV), variola, cowpox, and monkeypox viruses] encode both R1 and R2 subunits, the vast majority of Chordopoxviruses encode only R2 subunits. Using plaque morphology, growth curve, and mouse model studies, we investigated the requirement of VACV R1 (I4) and R2 (F4) subunits for replication and pathogenesis using a panel of mutant viruses in which one or more viral RR genes had been inactivated. Surprisingly, VACV F4, but not I4, was required for efficient replication in culture and virulence in mice. The growth defects of VACV strains lacking F4 could be complemented by genes encoding other Chordopoxvirus R2 subunits, suggesting conservation of function between poxvirus R2 proteins. Expression of F4 proteins encoding a point mutation predicted to inactivate RR activity but still allow for interaction with R1 subunits, caused a dominant negative phenotype in growth experiments in the presence or absence of I4. Co-immunoprecipitation studies showed that F4 (as well as other Chordopoxvirus R2 subunits) form hybrid complexes with cellular R1 subunits. Mutant F4 proteins that are unable to interact with host R1 subunits failed to rescue the replication defect of strains lacking F4, suggesting that F4-host R1 complex formation is critical for VACV replication. Our results suggest that poxvirus R2 subunits form functional complexes with host R1 subunits to provide sufficient dNTPs for viral replication. Our results also suggest that R2-deficient poxviruses may be selective oncolytic agents and our bioinformatic analyses provide insights into how poxvirus nucleotide metabolism proteins may have influenced the base composition of these pathogens.
核糖核苷酸还原酶(RRs)是进化上保守的酶,在哺乳动物中催化 dNTP 合成的限速步骤。RR 由大(R1)和小(R2)亚基组成,这两个亚基都是 R1(2)R2(2)杂四聚体复合物催化所必需的。痘病毒也编码 RR 蛋白,但感染人类的正痘病毒[例如,牛痘(VACV)、天花、牛痘和猴痘病毒]编码 R1 和 R2 亚基,而绝大多数的腔肠痘病毒只编码 R2 亚基。我们使用噬菌斑形态、生长曲线和小鼠模型研究,使用一组 RR 基因失活的突变病毒研究 VACV R1(I4)和 R2(F4)亚基对复制和发病机制的需求。令人惊讶的是,VACV F4,但不是 I4,是在培养中有效复制和在小鼠中毒力所必需的。缺乏 F4 的 VACV 株的生长缺陷可以通过编码其他腔肠痘病毒 R2 亚基的基因来互补,这表明痘病毒 R2 蛋白之间存在功能保守性。表达预测失活 RR 活性但仍允许与 R1 亚基相互作用的 F4 蛋白的点突变,在存在或不存在 I4 的情况下,在生长实验中引起显性负表型。共免疫沉淀研究表明,F4(以及其他腔肠痘病毒 R2 亚基)与细胞 R1 亚基形成杂合复合物。无法与宿主 R1 亚基相互作用的突变 F4 蛋白未能挽救缺乏 F4 的菌株的复制缺陷,这表明 F4-宿主 R1 复合物的形成对 VACV 的复制至关重要。我们的结果表明,痘病毒 R2 亚基与宿主 R1 亚基形成功能性复合物,为病毒复制提供足够的 dNTP。我们的结果还表明,R2 缺陷型痘病毒可能是选择性溶瘤剂,我们的生物信息学分析提供了有关痘病毒核苷酸代谢蛋白如何影响这些病原体的碱基组成的见解。