Martin D W, Deb S P, Klauer J S, Deb S
Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758.
J Virol. 1991 Aug;65(8):4359-69. doi: 10.1128/JVI.65.8.4359-4369.1991.
The herpes simplex virus type 1 (HSV-1) OriS region resides within a 90-bp sequence that contains two binding sites for the origin-binding protein (OBP), designated sites I and II. A third presumptive OBP-binding site (III) within OriS has strong sequence similarity to sites I and II, but no sequence-specific OBP binding has yet been demonstrated at this site. We have generated mutations in sites I, II, and III and determined their replication efficiencies in a transient in vivo assay in the presence of a helper virus. Mutations in any one of the sites reduced DNA replication significantly. To study the role of OriS sequence elements in site I and the presumptive site III in DNA replication, we have also generated a series of mutations that span from site I across the presumptive binding site III. These mutants were tested for their ability to replicate and for the ability to bind OBP by using gel shift analyses. The results indicate that mutations across site I drastically reduce DNA replication. Triple-base-pair substitution mutations that fall within the crucial OBP-binding domain, 5'-YGYTCGCACT-3' (where Y represents C or T), show a reduced level of OBP binding and DNA replication. Substitution mutations in site I that are outside this crucial binding sequence show a more detrimental effect on DNA replication than on OBP binding. This suggests that these sequences are required for initiation of DNA replication but are not critical for OBP binding. Mutations across the presumptive OBP-binding site III also resulted in a loss in efficiency of DNA replication. These mutations influenced OBP binding to OriS in gel shift assays, even though the mutated sequences are not contained within known OBP-binding sites. Replacement of the wild-type site III with a perfect OBP-binding site I results in a drastic reduction of DNA replication. Thus, our DNA replication assays and in vitro DNA-binding studies suggest that the binding of the origin sequence by OBP is not the only determining factor for initiation of DNA replication in vivo.
单纯疱疹病毒1型(HSV-1)的OriS区域位于一段90个碱基对的序列内,该序列包含两个与起始结合蛋白(OBP)的结合位点,分别命名为位点I和位点II。OriS内的第三个假定OBP结合位点(III)与位点I和位点II具有很强的序列相似性,但尚未在该位点证明有序列特异性的OBP结合。我们在位点I、II和III中产生了突变,并在存在辅助病毒的情况下,通过体内瞬时试验确定了它们的复制效率。任何一个位点的突变都会显著降低DNA复制。为了研究OriS序列元件在位点I和假定位点III在DNA复制中的作用,我们还产生了一系列从位点I跨越假定结合位点III的突变。通过凝胶迁移分析测试了这些突变体的复制能力和结合OBP的能力。结果表明,跨越位点I的突变会大幅降低DNA复制。位于关键OBP结合域5'-YGYTCGCACT-3'(其中Y代表C或T)内的三碱基对取代突变,显示出OBP结合水平和DNA复制水平降低。在位点I中位于这个关键结合序列之外的取代突变对DNA复制的影响比对OBP结合的影响更大。这表明这些序列是DNA复制起始所必需的,但对OBP结合并不关键。跨越假定OBP结合位点III的突变也导致DNA复制效率丧失。这些突变在凝胶迁移试验中影响了OBP与OriS的结合,尽管突变序列并不包含在已知的OBP结合位点内。用完美的OBP结合位点I替换野生型位点III会导致DNA复制大幅减少。因此,我们的DNA复制试验和体外DNA结合研究表明,OBP与起始序列的结合不是体内DNA复制起始的唯一决定因素。