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卡波西肉瘤相关疱疹病毒潜伏起源最小复制子的特性分析

Characterization of the minimal replicator of Kaposi's sarcoma-associated herpesvirus latent origin.

作者信息

Hu Jianhong, Renne Rolf

机构信息

Division of Hematology/Oncology and Department of Molecular Genetics and Microbiology, Case Western Reserve University, Cleveland, OH, USA.

出版信息

J Virol. 2005 Feb;79(4):2637-42. doi: 10.1128/JVI.79.4.2637-2642.2005.

Abstract

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.

摘要

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。

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