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Kaposi's Sarcoma-associated Herpesvirus (KSHV) Encodes a SUMO E3 ligase That Is SIM-dependent and SUMO-2/3-specific*

机译:卡波西氏肉瘤相关疱疹病毒(KSHV)编码SUMO E3连接酶,该酶依赖于SIM且具有SUMO-2 / 3特异性*

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摘要

Sumoylation has emerged as a major post-translational modification of cellular proteins, affecting a variety of cellular processes. Viruses have exploited the sumoylation pathway to advance their own replication by evolving several ways to perturb the host sumoylation apparatus. However, there has been no report of virally encoded enzymes directly involved in catalyzing the sumoylation reaction. Here, we report that the K-bZIP protein encoded by Kaposi's sarcoma-associated herpesvirus (KSHV) is a SUMO E3 ligase with specificity toward SUMO2/3. K-bZIP is a nuclear factor that functions to modulate viral gene expression and to prolong the G1 phase, allowing viral transcription and translation to proceed at the early stage of infection. In addition to functioning as a transcriptional factor, we show that K-bZIP carries a SIM (SUMO-interacting motif), which specifically binds to SUMO-2/3 but not SUMO-1. K-bZIP catalyzes its own SUMO modification as well as that of its interacting partners such as the cellular tumor suppressor proteins p53 and Rb, both in vitro and in vivo. This reaction depends on an intact SIM. Sumoylation of p53 leads to its activation and K-bZIP is recruited to several p53 target chromatin sites in a SIM-dependent manner. In addition to the identification of a viral SUMO-2/3 E3 ligase, our results provide additional insights into the mechanisms whereby K-bZIP induces cell cycle arrest.
机译:糖基化已经成为细胞蛋白的主要翻译后修饰,影响了多种细胞过程。病毒通过发展几种扰动宿主SUMO化设备的方法,利用SUMO化途径来促进自身复制。但是,尚无直接参与催化SUMO化反应的病毒编码酶的报道。在这里,我们报道由卡波济氏肉瘤相关疱疹病毒(KSHV)编码的K-bZIP蛋白是一种SUMO E3连接酶,对SUMO2 / 3具有特异性。 K-bZIP是一种核因子,其功能是调节病毒基因表达并延长G1期,从而使病毒的转录和翻译在感染的早期进行。除了起转录因子的作用外,我们还显示K-bZIP带有一个SIM(SUMO相互作用基序),它可以与SUMO-2 / 3特异性结合,但不能与SUMO-1结合。在体外和体内,K-bZIP都可催化自身的SUMO修饰及其相互作用的伴侣,例如细胞肿瘤抑制蛋白p53和Rb。此反应取决于完整的SIM卡。 p53的糖基化导致其激活,并且K-bZIP以SIM依赖的方式募集到几个p53靶染色质位点。除了鉴定病毒SUMO-2 / 3 E3连接酶外,我们的结果还提供了有关K-bZIP诱导细胞周期停滞的机制的更多见解。

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