González Carlos M, Wong Emily L, Bowser Brian S, Hong Gregory K, Kenney Shannon, Damania Blossom
Lineberger Comprehensive Cancer Center, CB#7295, University of North Carolina--Chapel Hill, North Carolina 27599, USA.
J Virol. 2006 Mar;80(6):3062-70. doi: 10.1128/JVI.80.6.3062-3070.2006.
Kaposi's sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's disease. Kaposi's sarcoma is the most common neoplasm among human immunodeficiency virus-positive individuals. Like other herpesviruses, KSHV is able to establish a predominantly latent, life-long infection in its host. The KSHV lytic cycle can be triggered by a number of stimuli that induce the expression of the key lytic switch protein, the replication and transcription activator (RTA) encoded by Orf50. The expression of Rta is necessary and sufficient to trigger the full lytic program resulting in the ordered expression of viral proteins, release of viral progeny, and host cell death. We have characterized an unknown open reading frame, Orf49, which lies adjacent and in the opposite orientation to Orf50. Orf49 is expressed during the KSHV lytic cycle and shows early transcription kinetics. We have mapped the 5' and 3' ends of the unspliced Orf49 transcript, which encodes a 30-kDa protein that is localized to both the nucleus and the cytoplasm. Interestingly, we found that Orf49 was able to cooperate with Rta to activate several KSHV lytic promoters containing AP-1 sites. The Orf49-encoded protein was also able to induce transcriptional activation through c-Jun but not the ATF1, ATF2, or CREB transcription factor. We found that Orf49 could induce phosphorylation and activation of the transcription factor c-Jun, the Jun N-terminal kinase (JNK), and p38. Our data suggest that Orf49 functions to activate the JNK and p38 pathways during the KSHV lytic cycle.
卡波西肉瘤相关疱疹病毒(KSHV)是卡波西肉瘤、原发性渗出性淋巴瘤和多中心Castleman病的病原体。卡波西肉瘤是人类免疫缺陷病毒阳性个体中最常见的肿瘤。与其他疱疹病毒一样,KSHV能够在其宿主中建立主要为潜伏性的终身感染。KSHV的裂解周期可由多种刺激触发,这些刺激诱导关键裂解开关蛋白即由Orf50编码的复制和转录激活因子(RTA)的表达。Rta的表达对于触发完整的裂解程序是必要且充分的,该程序导致病毒蛋白的有序表达、病毒后代的释放以及宿主细胞死亡。我们鉴定了一个未知的开放阅读框Orf49,它与Orf50相邻且方向相反。Orf49在KSHV裂解周期中表达,并表现出早期转录动力学。我们绘制了未剪接的Orf49转录本的5'和3'末端,该转录本编码一种30 kDa的蛋白质,定位于细胞核和细胞质。有趣的是,我们发现Orf49能够与Rta协同激活几个含有AP-1位点的KSHV裂解启动子。Orf49编码的蛋白质还能够通过c-Jun而非ATF1、ATF2或CREB转录因子诱导转录激活。我们发现Orf49可以诱导转录因子c-Jun、Jun N末端激酶(JNK)和p38的磷酸化和激活。我们的数据表明,Orf49在KSHV裂解周期中发挥作用,激活JNK和p38途径。