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卡波西肉瘤相关疱疹病毒(人类疱疹病毒8型)的潜伏相关核抗原与活化转录因子4/环磷腺苷效应元件结合蛋白2结合,并抑制其转录激活活性。

Latency-associated nuclear antigen of Kaposi's sarcoma-associated herpesvirus (human herpesvirus-8) binds ATF4/CREB2 and inhibits its transcriptional activation activity.

作者信息

Lim Chunghun, Sohn Hekwang, Gwack Yousang, Choe Joonho

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejeon 305-701, Korea1.

出版信息

J Gen Virol. 2000 Nov;81(Pt 11):2645-2652. doi: 10.1099/0022-1317-81-11-2645.

Abstract

Latency-associated nuclear antigen (LANA), encoded by ORF 73 of Kaposi's sarcoma-associated herpesvirus (KSHV; human herpesvirus-8), may play an important role in the persistence of the viral episome by tethering it to host chromosomes during mitosis. It also has been suggested from its amino acid sequence features that LANA may have transcription-regulatory activity. Here, it is reported that LANA interacts with activating transcription factor (ATF) 4/cAMP response element-binding protein (CREB) 2, a member of the ATF/CREB family of transcription factors, and represses the transcriptional activation activity of ATF4/CREB2. Repression by LANA is independent of the DNA-binding ability of ATF4/CREB2, since LANA also represses transactivation of ATF4/CREB2 fused to the GAL4 DNA-binding domain and does not affect the DNA-binding ability of ATF4/CREB2 in an electrophoretic mobility shift assay. The putative leucine zipper domain of LANA is required for binding to the relatively conserved basic region/leucine zipper domain (bZIP) of ATF4/CREB2, suggesting that the interaction may involve leucine zipper dimerization.

摘要

潜伏期相关核抗原(LANA)由卡波西肉瘤相关疱疹病毒(KSHV;人类疱疹病毒8型)的开放阅读框73编码,它可能通过在有丝分裂期间将病毒附加体拴系到宿主染色体上,在病毒附加体的持续存在中发挥重要作用。从其氨基酸序列特征也可推测,LANA可能具有转录调节活性。在此报道,LANA与转录激活因子(ATF)4/环磷酸腺苷反应元件结合蛋白(CREB)2相互作用,ATF4/CREB2是ATF/CREB转录因子家族的成员,LANA可抑制ATF4/CREB2的转录激活活性。LANA的抑制作用独立于ATF4/CREB2的DNA结合能力,因为LANA也抑制与GAL4 DNA结合结构域融合的ATF4/CREB2的反式激活,并且在电泳迁移率变动分析中不影响ATF4/CREB2的DNA结合能力。LANA的假定亮氨酸拉链结构域对于与ATF4/CREB2相对保守的碱性区域/亮氨酸拉链结构域(bZIP)结合是必需的,这表明这种相互作用可能涉及亮氨酸拉链二聚化。

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