Knopf C W, Spies B, Kaerner H C
Nucleic Acids Res. 1986 Nov 11;14(21):8655-67. doi: 10.1093/nar/14.21.8655.
The nucleotide sequences of the origins of DNA replication (ori) of the S- and L-component (oriS, oriL) of the herpes simplex virus type 1 (HSV-1) standard genome were determined from HSV-1 strain Angelotti (ANG). In contrast to other HSV-1 strains, the ANG oriS sequence revealed an insertion of an TA-dinucleotide in an otherwise very conserved but imperfect palindromic sequence of 47 bp. The oriL sequence of the standard ANG genome was found to be identical to that of an ANG class II defective genome which exhibits a duplication of a 144 bp palindrome. A model is presented to explain the origination of the amplified ANG oriL sequences from the parental genome with a single copy of oriL via illegitimate recombination. Alignment of the ori sequences of HSV, adeno- and papovaviruses unveiled that the HSV ori region can be subdivided into two distinct sites of homology to the DNA initiation signals of papova- and adenoviruses, suggesting that the HSV origins of replication comprise elements for DNA replication by both, cellular and virus-encoded DNA polymerases.
从单纯疱疹病毒1型(HSV-1)标准基因组的S和L成分(oriS、oriL)的DNA复制起点(ori)的核苷酸序列是从HSV-1安杰洛蒂毒株(ANG)中确定的。与其他HSV-1毒株不同,ANG oriS序列显示在一个47 bp的、原本非常保守但不完美的回文序列中插入了一个TA二核苷酸。发现标准ANG基因组的oriL序列与ANG II类缺陷基因组的oriL序列相同,后者表现出一个144 bp回文序列的重复。提出了一个模型来解释通过非法重组从具有单个oriL拷贝的亲本基因组中产生扩增的ANG oriL序列。HSV、腺病毒和乳头瘤病毒的ori序列比对显示,HSV ori区域可细分为与乳头瘤病毒和腺病毒的DNA起始信号有两个不同同源性的位点,这表明HSV复制起点包含细胞和病毒编码的DNA聚合酶进行DNA复制的元件。