Li Shijun, Tan Min, Juillard Franceline, Ponnusamy Rajesh, Correia Bruno, Simas J Pedro, Carrondo Maria A, McVey Colin E, Kaye Kenneth M
Departments of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, 02115.
Instituto de Tecnologia Quimica e Biologica, Universidade Nova de Lisboa, 2781-901 Oeiras, Portugal.
J Biol Chem. 2015 Nov 20;290(47):28084-28096. doi: 10.1074/jbc.M115.674622. Epub 2015 Sep 29.
Kaposi sarcoma-associated herpesvirus (KSHV) has a causative role in several human malignancies. KSHV latency-associated nuclear antigen (LANA) mediates persistence of viral episomes in latently infected cells. LANA mediates KSHV DNA replication and segregates episomes to progeny nuclei. The structure of the LANA DNA binding domain was recently solved, revealing a positive electrostatic patch opposite the DNA binding surface, which is the site of BET protein binding. Here we investigate the functional role of the positive patch in LANA-mediated episome persistence. As expected, LANA mutants with alanine or glutamate substitutions in the central, peripheral, or lateral portions of the positive patch maintained the ability to bind DNA by EMSA. However, all of the substitution mutants were deficient for LANA DNA replication and episome maintenance. Mutation of the peripheral region generated the largest deficiencies. Despite these deficiencies, all positive patch mutants concentrated to dots along mitotic chromosomes in cells containing episomes, similar to LANA. The central and peripheral mutants, but not the lateral mutants, were reduced for BET protein interaction as assessed by co-immunoprecipitation. However, defects in BET protein binding were independent of episome maintenance function. Overall, the reductions in episome maintenance closely correlated with DNA replication deficiencies, suggesting that the replication defects account for the reduced episome persistence. Therefore, the electrostatic patch exerts a key role in LANA-mediated DNA replication and episome persistence and may act through a host cell partner(s) other than a BET protein or by inducing specific structures or complexes.
卡波西肉瘤相关疱疹病毒(KSHV)在多种人类恶性肿瘤中具有致病作用。KSHV潜伏相关核抗原(LANA)介导病毒附加体在潜伏感染细胞中的持续存在。LANA介导KSHV DNA复制并将附加体分离到子代细胞核中。LANA DNA结合结构域的结构最近得到解析,揭示了与DNA结合表面相对的正电荷静电斑块,这是BET蛋白结合的位点。在此,我们研究了正电荷斑块在LANA介导的附加体持续存在中的功能作用。正如预期的那样,在正电荷斑块的中央、周边或侧面部分用丙氨酸或谷氨酸替代的LANA突变体通过电泳迁移率变动分析(EMSA)仍保持结合DNA的能力。然而,所有替代突变体在LANA DNA复制和附加体维持方面均存在缺陷。周边区域的突变产生的缺陷最大。尽管存在这些缺陷,但在含有附加体的细胞中,所有正电荷斑块突变体都像LANA一样沿着有丝分裂染色体浓缩成点。通过免疫共沉淀评估,中央和周边突变体,但不是侧面突变体,与BET蛋白的相互作用减少。然而,BET蛋白结合缺陷与附加体维持功能无关。总体而言,附加体维持的减少与DNA复制缺陷密切相关,表明复制缺陷导致附加体持续存在减少。因此,静电斑块在LANA介导的DNA复制和附加体持续存在中发挥关键作用,可能通过除BET蛋白之外的宿主细胞伙伴起作用,或者通过诱导特定结构或复合物起作用。