Wides R J, Challberg M D, Rawlins D R, Kelly T J
Mol Cell Biol. 1987 Feb;7(2):864-74. doi: 10.1128/mcb.7.2.864-874.1987.
The initiation of adenovirus DNA takes place at the termini of the viral genome and requires the presence of specific nucleotide sequence elements. To define the sequence organization of the viral origin, we tested a large number of deletion, insertion, and base substitution mutants for their ability to support initiation and replication in vitro. The data demonstrate that the origin consists of at least three functionally distinct domains, A, B, and C. Domain A (nucleotides 1 to 18) contains the minimal sequence sufficient for origin function. Domains B (nucleotides 19 to 40) and C (nucleotides 41 to 51) contain accessory sequences that significantly increase the activity of the minimal origin. The presence of domain B increases the efficiency of initiation by more than 10-fold in vitro, and the presence of domains B and C increases the efficiency of initiation by more than 30-fold. Mutations that alter the distance between the minimal origin and the accessory domains by one or two base pairs dramatically decrease initiation efficiency. This critical spacing requirement suggests that there are specific interactions between the factors that recognize the two regions.
腺病毒DNA的起始发生在病毒基因组的末端,并且需要特定核苷酸序列元件的存在。为了确定病毒起源的序列组织,我们测试了大量的缺失、插入和碱基替换突变体在体外支持起始和复制的能力。数据表明,起源至少由三个功能不同的结构域A、B和C组成。结构域A(核苷酸1至18)包含足以实现起源功能的最小序列。结构域B(核苷酸19至40)和C(核苷酸41至51)包含显著增加最小起源活性的辅助序列。结构域B的存在使体外起始效率提高了10倍以上,结构域B和C的存在使起始效率提高了30倍以上。将最小起源与辅助结构域之间的距离改变一两个碱基对的突变会显著降低起始效率。这种关键的间距要求表明,识别这两个区域的因子之间存在特定的相互作用。