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Updated: Jun 25, 2026

Examination of Pyroptosis by Flow Cytometry
Published on: May 31, 2024
Apoptosis-inducing proteins in chicken anemia virus and TT virus
1Department of Molecular Genetics, Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333 CC Leiden, The Netherlands. m.smit@chem.leidenuniv.nl
Abstract:
Torque teno viruses (TTVs) share several genomic similarities with the chicken anemia virus (CAV). CAV encodes the protein apoptin that specifically induces apoptosis in (human) tumor cells. Functional studies reveal that apoptin induces apoptosis in a very broad range of (human) tumor cells. A putative TTV open reading frame (ORF) in TTV genotype 1, named TTV apoptosis inducing protein (TAIP), it induces, like apoptin, p53-independent apoptosis in various human hepatocarcinoma cell lines to a similar level as apoptin. In comparison to apoptin, TAIP action is less pronounced in several analyzed human non-hepatocarcinoma-derived cell lines. Detailed sequence analysis has revealed that the TAIP ORF is conserved within a limited group of the heterogeneous TTV population. However, its N-terminal half, N-TAIP, is rather well conserved in a much broader set of TTV isolates. The similarities between apoptin and TAIP, and their relevance for the development and treatment of diseases is discussed.
Insights
Torque teno viruses (TTVs) possess a protein, TAIP, that induces apoptosis in human tumor cells, similar to chicken anemia virus
Area of Science:
- Virology
- Molecular Biology
- Oncology
Background:
- Torque teno viruses (TTVs) exhibit genomic similarities to chicken anemia virus (CAV).
- CAV encodes the protein apoptin, known for inducing apoptosis in human tumor cells.
- Apoptin demonstrates broad-spectrum apoptosis induction in diverse human tumor cell lines.
Purpose of the Study:
- To investigate a putative TTV open reading frame (ORF) in TTV genotype 1, named TAIP.
- To compare the apoptosis-inducing capabilities of TAIP with CAV's apoptin.
- To analyze the conservation and potential therapeutic relevance of TAIP.
Main Methods:
- Functional studies of TAIP in various human hepatocarcinoma and non-hepatocarcinoma cell lines.
- Comparative analysis of TAIP and apoptin's apoptosis-inducing activity.
- Detailed sequence analysis of the TAIP ORF and its N-terminal half (N-TAIP) across TTV isolates.
Main Results:
- TAIP induces p53-independent apoptosis in human hepatocarcinoma cell lines, comparable to apoptin.
- TAIP's apoptotic effect is less pronounced in non-hepatocarcinoma cell lines compared to apoptin.
- The TAIP ORF is conserved in a subset of TTVs, while N-TAIP is broadly conserved among TTV isolates.
Conclusions:
- TAIP represents a TTV-encoded protein with significant apoptosis-inducing potential, particularly in liver cancer cells.
- The conserved N-TAIP region suggests a potential role in TTV biology and possible therapeutic applications.
- Further research into TAIP and apoptin similarities may offer insights into disease development and treatment strategies.
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