首页> 外文期刊>The Journal of biological chemistry >Kaposi's Sarcoma-associated Herpesvirus (KSHV) Encodes a SUMO E3 ligase That Is SIM-dependent and SUMO-2/3-specific
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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:Kaposi的Sarcoma相关的Herpesvirus(KSHV)编码了SIMO E3连接酶,它是SIM依赖和SUMO-2/3特定的

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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:Sumoylation已成为细胞蛋白的主要翻译后修饰,影响各种细胞过程。病毒利用Sublation途径通过演变几种来扰乱主机象限装置来推进自己的复制。然而,没有直接参与催化Sublation反应的病毒编码酶的报道。在这里,我们报告说,由Kaposi的肉瘤相关的Herpesvirus(Kshv)编码的K-Bzip蛋白是Sumo E3连接酶,其具有比SuMO2 / 3的特异性。 K-BZIP是一种核因子,其用于调节病毒基因表达并延长G1相,允许病毒转录和翻译在感染的早期进行。除了用作转录因子之外,我们还表明K-BZIP承载SIM(相互作用的基序),其特异性结合SUMO-2/3但不是SUMO-1。 K-BZIP催化其自身的SUMO改性以及其相互作用的伴侣,例如细胞肿瘤抑制剂蛋白P53和RB,在体外和体内。该反应取决于完整的SIM卡。 P53的Sumoylation将其激活,并且以SIM依赖性方式募集到几个P53靶染色质位点K-Bzip。除了鉴定病毒SUMO-2/3 E3连接酶外,我们的结果还提供了k-bzip诱导细胞周期停滞的机制的额外见解。

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