Regulation of the Abundance of Kaposi’s Sarcoma-Associated Herpesvirus ORF50 Protein by Oncoprotein MDM2

PLoS Pathogens

Li-Kwan Chang¹  Pey-Jium Chang²  Shie-Shan Wang³  Lee-Wen Chen⁴  Tzu-Hsuan Chang⁵  Shih-Tung Liu⁵  Ying-Ju Shih⁶ 

[1] Department of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei, Taiwan;Department of Microbiology and Immunology, College of Medicine, Chang-Gung University, Taoyuan, Taiwan;Department of Pediatric Surgery, Chang-Gung Memorial Hospital, Chiayi, Taiwan;Department of Respiratory Care, Chang-Gung University of Science and Technology, Chiayi, Taiwan;Graduate Institute of Biomedical Sciences, College of Medicine, Chang-Gung University, Taoyuan, Taiwan;Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang-Gung University, Taoyuan, Taiwan

关键词: 293T cells;    Immunoprecipitation;    Immunoblotting;    Lysine;    Ubiquitination;    Protein abundance;    Ligases;    Cytoplasm;   

DOI  :  10.1371/journal.ppat.1005918

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

The switch between latency and the lytic cycle of Kaposi’s sarcoma-associated herpesvirus (KSHV) is controlled by the expression of virally encoded ORF50 protein. Thus far, the regulatory mechanism underlying the protein stability of ORF50 is unknown. Our earlier studies have demonstrated that a protein abundance regulatory signal (PARS) at the ORF50 C-terminal region modulates its protein abundance. The PARS region consists of PARS-I (aa 490–535) and PARS-II (aa 590–650), and mutations in either component result in abundant expression of ORF50. Here, we show that ORF50 protein is polyubiquitinated and its abundance is controlled through the proteasomal degradation pathway. The PARS-I motif mainly functions as a nuclear localization signal in the control of ORF50 abundance, whereas the PARS-II motif is required for the binding of ubiquitin enzymes in the nucleus. We find that human oncoprotein MDM2, an ubiquitin E3 ligase, is capable of interacting with ORF50 and promoting ORF50 degradation in cells. The interaction domains between both proteins are mapped to the PARS region of ORF50 and the N-terminal 220-aa region of MDM2. Additionally, we identify lysine residues at positions 152 and 154 in the N-terminal domain of ORF50 critically involved in MDM2-mediated downregulation of ORF50 levels. Within KSHV-infected cells, the levels of MDM2 were greatly reduced during viral lytic cycle and genetic knockdown of MDM2 in these cells favored the enhancement of ORF50 expression, supporting that MDM2 is a negative regulator of ORF50 expression. Collectively, the study elucidates the regulatory mechanism of ORF50 stability and implicates that MDM2 may have a significant role in the maintenance of viral latency by lowering basal level of ORF50.

【 授权许可】

CC BY