Boehmer P E, Lehman I R
Department of Biochemistry, Beckman Center, Stanford University School of Medicine, California 94305-5307.
J Virol. 1993 Feb;67(2):711-5. doi: 10.1128/JVI.67.2.711-715.1993.
The major single-stranded DNA-binding protein, ICP8, of herpes simplex virus type 1 (HSV-1) is one of seven virus-encoded polypeptides required for HSV-1 DNA replication. To investigate the role of ICP8 in viral DNA replication, we have examined the interaction of ICP8 with partial DNA duplexes and found that it can displace oligonucleotides annealed to single-stranded M13 DNA. In addition, ICP8 can melt small fragments of fully duplex DNA. Unlike a DNA helicase, ICP8-promoted strand displacement is ATP and Mg2+ independent and exhibits no directionality. It requires saturating amounts of ICP8 and is both efficient and highly cooperative. These properties make ICP8 suitable for a role in DNA replication in which ICP8 destabilizes duplex DNA during origin unwinding and replication fork movement.
单纯疱疹病毒1型(HSV-1)的主要单链DNA结合蛋白ICP8是HSV-1 DNA复制所需的七种病毒编码多肽之一。为了研究ICP8在病毒DNA复制中的作用,我们检测了ICP8与部分DNA双链体的相互作用,发现它可以取代退火到单链M13 DNA上的寡核苷酸。此外,ICP8可以使完全双链DNA的小片段解链。与DNA解旋酶不同,ICP8促进的链置换不依赖ATP和Mg2+,且没有方向性。它需要饱和量的ICP8,并且高效且高度协同。这些特性使ICP8适合在DNA复制中发挥作用,即在起始点解旋和复制叉移动过程中使双链DNA不稳定。