Hu Jianhong, Renne Rolf
Division of Hematology/Oncology and Department of Molecular Genetics and Microbiology, Case Western Reserve University, Cleveland, OH, USA.
J Virol. 2005 Feb;79(4):2637-42. doi: 10.1128/JVI.79.4.2637-2642.2005.
The latency-associated nuclear antigen (LANA) of Kaposi's sarcoma-associated herpesvirus (KSHV) binds to two sites within the 801-bp-long terminal repeat (TR) and is the only viral protein required for episomal maintenance. While two or more copies of TR are required for long-term maintenance, a single TR confers LANA-dependent origin activity on plasmid DNA. Deletion mapping revealed a 71-bp-long minimal replicator containing two distinctive sequence elements: LANA binding sites (LBS1/2) and an adjacent 29- to 32-bp-long GC-rich sequence which we termed the replication element. Furthermore, the transcription factor Sp1 can bind to TR outside the minimal replicator and contributes to TR's previously reported enhancer activity.
卡波西肉瘤相关疱疹病毒(KSHV)的潜伏相关核抗原(LANA)与801bp长的末端重复序列(TR)内的两个位点结合,并且是游离型维持所必需的唯一病毒蛋白。虽然长期维持需要两个或更多拷贝的TR,但单个TR可赋予质粒DNA上依赖LANA的起始活性。缺失作图揭示了一个71bp长的最小复制子,其包含两个独特的序列元件:LANA结合位点(LBS1/2)和相邻的29至32bp长的富含GC的序列,我们将其称为复制元件。此外,转录因子Sp1可以结合最小复制子外的TR,并有助于TR先前报道的增强子活性。