Eckert Dawn, Williams Ollie, Meseda Clement A, Merchlinsky Michael
Laboratory of DNA Viruses, Division of Viral Products, Center for Biologics Evaluation and Research, Food and Drug Administration, HFM-457, 1401 Rockville Pike, Rockville, MD 20852-1448, USA.
J Virol. 2005 Dec;79(24):15084-90. doi: 10.1128/JVI.79.24.15084-15090.2005.
Vaccinia virus encodes an enzyme with DNA modifying activity that cleaves and inefficiently cross-links cruciformic DNA. This enzyme is contained within the virion, expressed at late times postinfection, and processes DNA in an energy-independent, Mg2+ ion-independent manner. Viral nuclease activity was measured in extracts from cells infected with well-defined viral mutants. Since some viral extracts lacked nuclease activity, the gene encoding the activity was postulated to be one of the open reading frames absent in the viruses lacking activity. Inducible expression of each candidate open reading frame revealed that only the gene VACWR035, or K4L, was required for nuclease activity. A recombinant virus missing only the open reading frame for K4L lacked nuclease activity. Extracts from a recombinant virus expressing K4L linked to a FLAG polypeptide were able to cleave and cross-link cruciformic DNA. There were no significant differences between the virus lacking K4L and wild-type vaccinia virus WR with respect to infectivity, growth characteristics, or processing of viral replicative intermediate DNA, including both telomeric and cross-linked forms. Purification of the K4L FLAG polypeptide expressed in bacteria yielded protein containing nicking-joining activity, implying that K4L is the only vaccinia virus protein required for the nicking-joining enzymatic activity.
痘苗病毒编码一种具有DNA修饰活性的酶,该酶可切割并低效交联十字形DNA。这种酶存在于病毒粒子中,在感染后期表达,并以能量非依赖性、Mg2+离子非依赖性方式处理DNA。在感染了明确的病毒突变体的细胞提取物中测量病毒核酸酶活性。由于一些病毒提取物缺乏核酸酶活性,因此推测编码该活性的基因是缺乏活性的病毒中不存在的开放阅读框之一。每个候选开放阅读框的诱导表达表明,只有基因VACWR035或K4L是核酸酶活性所必需的。仅缺失K4L开放阅读框的重组病毒缺乏核酸酶活性。表达与FLAG多肽连接的K4L的重组病毒提取物能够切割并交联十字形DNA。在缺乏K4L的病毒与野生型痘苗病毒WR之间,在感染性、生长特性或病毒复制中间DNA(包括端粒形式和交联形式)的处理方面没有显著差异。在细菌中表达的K4L FLAG多肽的纯化产生了具有切口连接活性的蛋白质,这意味着K4L是切口连接酶活性所需的唯一痘苗病毒蛋白。