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. 2021 Feb 2;10:609071. doi: 10.3389/fcimb.2020.609071

Table 1.

Molecules that interact with CAV and PCV ORF3 proteins.

Viruses Cellular localization Interacting molecules Biological effects References
CAV Nucleus PML The disruption of the interaction between the PML and ORF3 proteins does not affect their cytotoxicities (Heilman et al., 2006)
CDK1 and CDK2 Induce ORF3 Thr108 phosphorylation; regulate ORF3 subcellular localization (Maddika et al., 2009; Zhao et al., 2013)
PKC β Make ORF3 phosphorylated (Jiang et al., 2010; Bullenkamp et al., 2015)
APC1 Induces cell cycle arrest in mitosis (Teodoro et al., 2004)
DEDAF
  • Increases apoptosis

(Danen-van Oorschot et al., 2004)
Cytoplasm Nmi May alter the activity of Nmi (Sun et al., 2002)
Importin β1 Facilitates ORF3 nuclear translocation (Poon et al., 2005; Kuusisto et al., 2008)
PI3K Activates PI3K and Akt; facilitates Akt nuclear translocation (Maddika et al., 2007; Maddika et al., 2008)
Hippi Co-localizes with ORF3 protein in the cytoplasm of non-cancerous cells, whereas in tumor cells, the ORF3 protein migrates to the nucleus and Hippi remains in the cytoplasm (Cheng et al., 2003)
Ppil3 Facilitates cytoplasmic localization of ORF3 (Huo et al., 2008)
FADD Co-localizes in so-called death effector filaments (Guelen et al., 2004)
Bcl10 Co-localizes to cytoplasmic filaments; regulates apoptosis and NF-κB activation (Guelen et al., 2004)
Hsp70 Inhibit the Hsp70 expression and reduce its transcription (Chen et al., 2011; Yuan et al., 2013)
Hsc70 Affects ORF3-induced Akt phosphorylation (Chen et al., 2011)
PCV Cytoplasm pPirh2 Leads to the accumulation of p53 and induction of a caspase cascade to apoptosis in the intrinsic pathway of apoptosis (Leng et al., 2003; Liu et al., 2007)
RGS16 Causes ubiquitin-mediated proteasomal degradation of RGS16 and increases NF-κB translocation into the nucleus through the ERK1/2 signaling pathway; induces an increase in IL-6 and IL-8 mRNA transcripts (Timmusk et al., 2009; Choi et al., 2015)
/ DDE-like transposase
  • No more information is available.

(Timmusk et al., 2006)