相扑蛋白
溶解循环
生物
抑制因子
基因沉默
病毒潜伏期
细胞生物学
转录因子
病毒复制
基因
病毒学
遗传学
泛素
病毒
作者
Qiliang Cai,Cai Shen,Caixia Zhu,Suhbash C. Verma,Ji-Young Choi,Erle S. Robertson
出处
期刊:PLOS Pathogens
[Public Library of Science]
日期:2013-11-21
卷期号:9 (11): e1003750-e1003750
被引量:58
标识
DOI:10.1371/journal.ppat.1003750
摘要
Kaposi's sarcoma-associated herpesvirus (KSHV) stabilizes hypoxia-inducible factor α (HIF-1α) during latent infection, and HIF-1α reactivates lytic replication under hypoxic stress. However, the mechanism utilized by KSHV to block lytic reactivation with the accumulation of HIF-1α in latency remains unclear. Here, we report that LANA encoded by KSHV contains a unique SUMO-interacting motif (LANASIM) which is specific for interaction with SUMO-2 and facilitates LANA SUMOylation at lysine 1140. Proteomic and co-immunoprecipitation analysis further reveal that the SUMO-2 modified transcription repressor KAP1 is a critical factor recruited by LANASIM. Deletion of LANASIM led to functional loss of both LANA-mediated viral episome maintenance and lytic gene silencing. Moreover, hypoxia reduced KAP1 SUMOylation and resulted in dissociation of both KAP1 and Sin3A repressors from LANASIM-associated complex. Therefore, the LANASIM motif plays an essential role in KSHV latency and is a potential drug target against KSHV-associated cancers.
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