Dean F B, Borowiec J A, Ishimi Y, Deb S, Tegtmeyer P, Hurwitz J
Graduate Program in Molecular Biology, Sloan Kettering Cancer Center, New York, NY 10021.
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8267-71. doi: 10.1073/pnas.84.23.8267.
Simian virus 40 (SV40) large tumor antigen (T antigen) unwinds DNA containing the SV40 origin of replication. The origin requirement for unwinding can be satisfied by the 64-base-pair SV40 core origin that supports T-antigen-dependent DNA replication both in vivo and in vitro. The core origin contains three domains with specific DNA sequence features. These include an inverted repeat, a central T-antigen binding domain, and an adenine- and thymine-rich domain containing a DNA bending focus. The domain and spacer requirements of the core origin for DNA unwinding and replication in vitro are strikingly similar to the origin requirements for DNA replication in vivo. Thus, each of the three functional domains of the core origin contributes directly to the initiation of duplex DNA unwinding by T antigen.
猴病毒40(SV40)大T抗原可解开含有SV40复制起点的DNA。支持体内和体外T抗原依赖性DNA复制的64个碱基对的SV40核心起点可满足解开DNA所需的起点要求。核心起点包含三个具有特定DNA序列特征的结构域。这些结构域包括一个反向重复序列、一个中央T抗原结合结构域以及一个富含腺嘌呤和胸腺嘧啶的结构域,该结构域含有一个DNA弯曲焦点。核心起点在体外进行DNA解旋和复制时对结构域和间隔区的要求与体内DNA复制对起点的要求极为相似。因此,核心起点的三个功能结构域中的每一个都直接促成了T抗原引发双链DNA解旋。