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VP2 of Chicken Anaemia Virus Interacts with Apoptin for Down-regulation of Apoptosis through De-phosphorylated Threonine 108 on Apoptin.
Lai, Guan-Hua; Lien, Yi-Yang; Lin, Ming-Kuem; Cheng, Jai-Hong; Tzen, Jason Tc; Sun, Fang-Chun; Lee, Meng-Shiunn; Chen, Hsi-Jien; Lee, Meng-Shiou.
Affiliation
  • Lai GH; Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, 40402, Taiwan.
  • Lien YY; Department of Veterinary Medicine, National Pingtung University of Science and Technology, Pingtung, 91201, Taiwan.
  • Lin MK; Department of Chinese Pharmaceutical Science and Chinese Medicine Resources, China Medical University, Taichung, 40402, Taiwan.
  • Cheng JH; Center for Shockwave Medicine and Tissue Engineering, Department of Medical Research, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, 83301, Taiwan.
  • Tzen JT; Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, 40402, Taiwan.
  • Sun FC; Department of Bioresources, Da-Yeh University, Changhua, 515, Taiwan.
  • Lee MS; Research Assistance Center, Show Chwan Memorial Hospital, Changhua, 500, Taiwan.
  • Chen HJ; Department of Safety, Health and Environmental Engineering, Ming Chi University of Technology, New Taipei, 24301, Taiwan.
  • Lee MS; Department of Chinese Pharmaceutical Science and Chinese Medicine Resources, China Medical University, Taichung, 40402, Taiwan. leemengshiou@mail.cmu.edu.tw.
Sci Rep ; 7(1): 14799, 2017 11 01.
Article in En | MEDLINE | ID: mdl-29093508
ABSTRACT
Chicken anaemia virus (CAV) is an important contagious agent that causes immunosuppressive disease in chickens. CAV Apoptin is a nucleoplasmic shuffling protein that induces apoptosis in chicken lymphoblastoid cells. In the present study, confocal microscopy revealed co-localisation of expressed CAV non-structural protein VP2 with Apoptin in the nucleus of MDCC-MSB1 cells and the nucleoplasmic compartment of CHO-K1 cells. In vitro pull-down and ex vivo biomolecular fluorescent complementation (BiFC) assays further showed that the VP2 protein directly interacts with Apoptin. Transient co-expression of VP2 and Apoptin in MDCC-MSB1 cells significantly decreased the rate of apoptosis compared with that in cells transfected with the Apoptin gene alone. In addition, the phosphorylation status of threonine 108 (Thr108) of Apoptin was found to decrease upon interaction with VP2. Although dephosphorylated Thr108 did not alter the subcellular distribution of Apoptin in the nucleus of MDCC-MSB1 cells, it did suppress apoptosis. These findings provide the first evidence that VP2 directly interacts with Apoptin in the nucleus to down-regulate apoptosis through alterations in the phosphorylation status of the latter. This information will be useful to further elucidate the underlying mechanism of viral replication in the CAV life cycle.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Virus Replication / Down-Regulation / Gene Expression Regulation, Viral / Apoptosis / Chicken anemia virus / Capsid Proteins Limits: Animals Language: En Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Virus Replication / Down-Regulation / Gene Expression Regulation, Viral / Apoptosis / Chicken anemia virus / Capsid Proteins Limits: Animals Language: En Year: 2017 Type: Article